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FILamentAGGRegatingproteIN&#41; &#233; uma prote&#237;na encontrada nos corne&#243;citos respons&#225;vel por agregar a queratina na forma&#231;&#227;o do estrato c&#243;rneo&#46;<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">3</span></a> &#201; produzida a partir de um precursor&#44; a pr&#243;&#8208;filagrina&#44; que se localiza na camada granulosa da epiderme nos gr&#226;nulos de querato hialina&#46; A pr&#243;&#8208;filagrina &#233; subsequentemente desfosforilada&#44; resulta na forma&#231;&#227;o de mon&#243;meros de filagrina que t&#234;m propriedades de agrega&#231;&#227;o de filamentos de queratina&#46; A degrada&#231;&#227;o da filagrina gera os fatores de hidrata&#231;&#227;o natural &#40;<span class="elsevierStyleItalic">Natural Mosturizing Factors</span> &#8722; NMFs&#41;&#44; que incluem amino&#225;cidos livres&#44; &#225;cido uroc&#226;nico &#40;UCA&#41; e &#225;cido pirrolid&#244;nico carbox&#237;lico &#40;PCA&#41;&#46; Os NMFs promovem capta&#231;&#227;o e aprisionamento da &#225;gua e manuten&#231;&#227;o do pH &#225;cido da pele&#44; essencial para o processo de hidrata&#231;&#227;o e manuten&#231;&#227;o da barreira cut&#226;nea&#46;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">4</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">O gene que codifica a filagrina est&#225; localizado no cromossomo&#160;1q21&#44; em uma regi&#227;o denominada complexo de diferencia&#231;&#227;o epid&#233;rmica&#46;<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">3</span></a> De acordo com a literatura&#59; 27&#44;5&#37; dos brancos americanos&#59; 48&#37; dos europeus&#59; 31&#44;4&#37; dos chineses e 20&#37; dos japoneses portadores de dermatite at&#243;pica apresentam muta&#231;&#245;es no gene da filagrina&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Atualmente 47&#160;muta&#231;&#245;es com perda de fun&#231;&#227;o j&#225; foram identificadas no gene que codifica a filagrina em pacientes com DA&#46; Perfis distintos de muta&#231;&#245;es foram identificados em pacientes da Europa e da &#193;sia&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">6</span></a> Entre as muta&#231;&#245;es descritas&#44; as mais comumente encontradas nos brancos s&#227;o a R501X e a 2282del4 &#40;compreendem 50&#37; do total&#41;&#44; al&#233;m da R2447X e da S3247X&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">7</span></a> Na popula&#231;&#227;o japonesa&#44; as principais muta&#231;&#245;es foram a 3321delA e a S2554X&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">8</span></a> Essas muta&#231;&#245;es parecem variar de acordo com grupos &#233;tnicos&#44; por exemplo&#44; na popula&#231;&#227;o negra estudos demonstraram uma preval&#234;ncia bem menor que nos brancos&#46;<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">9</span></a> Gao et al&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">10</span></a> encontraram a R501X em 3&#44;2&#37; &#91;U1&#93; de 187&#160;pacientes negros com dermatite at&#243;pica e nenhuma associa&#231;&#227;o com 2282del4&#46; J&#225; Margolis et al&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">7</span></a> avaliaram o gen&#243;tipo de 370&#160;negros com DA e encontraram muta&#231;&#245;es em apenas 1&#37; dos pacientes<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">8</span></a> &#40;R501X 3&#44;2&#37;&#59; 2282del4&#160;0&#44;5&#37;&#59; S3247X&#160;3&#37; e R2447X&#160;1&#44;4&#37;&#41;&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">A filagrina&#160;2 &#233; uma prote&#237;na com fun&#231;&#227;o semelhante &#224; filagrina e tamb&#233;m codificada na regi&#227;o denominada complexo de diferencia&#231;&#227;o da epiderme&#46; De acordo com Makino et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">11</span></a> a express&#227;o da prote&#237;na filagrina&#160;2 est&#225; diminu&#237;da em portadores de DA&#46; H&#225; relato de uma associa&#231;&#227;o entre polimorfismos no gene da filagrina&#160;2 &#40;rs&#160;12568784 e rs&#160;1689937411&#41; e DA persistente em pacientes negros portadores de dermatite at&#243;pica&#46;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">12</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">N&#227;o h&#225; estudos sobre a preval&#234;ncia de filagrina e filagrina&#160;2 na popula&#231;&#227;o brasileira&#46; O objetivo deste estudo foi avaliar os polimorfismos no gene da filagrina&#160;2 &#40;rs&#160;12568784 e rs&#160;16899374&#41; em crian&#231;as e adultos com dermatite at&#243;pica e verificar a associa&#231;&#227;o desses com a gravidade do quadro cl&#237;nico&#44; presen&#231;a de outras doen&#231;as al&#233;rgicas e fatores sociodemogr&#225;ficos&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">M&#233;todos</span><p id="par0045" class="elsevierStylePara elsevierViewall">Estudo transversal&#44; envolveu pacientes de ambos os sexos&#44; entre&#160;um&#160;e&#160;27&#160;anos&#44; com diagn&#243;stico de dermatite at&#243;pica&#44; de acordo com os crit&#233;rios da <span class="elsevierStyleItalic">United Kingdom Working Party</span> &#40;UK&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">13</span></a> recrutados nos ambulat&#243;rios de dermatite at&#243;pica&#46; Foram exclu&#237;dos aqueles com outras doen&#231;as cr&#244;nicas da pele &#40;psor&#237;ase&#44; entre outras&#41; ou doen&#231;as sist&#234;micas que afetam a pele&#44; como imunodefici&#234;ncias prim&#225;rias&#44; l&#250;pus eritematoso sist&#234;mico&#44; entre outras&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">De acordo com a ordem de chegada ao ambulat&#243;rio&#44; os pacientes responderam a um question&#225;rio com as seguintes vari&#225;veis&#58; sexo&#44; idade&#44; etnia&#44; in&#237;cio da DA&#44; hist&#243;ria familiar de doen&#231;as al&#233;rgicas e presen&#231;a de asma&#44; alergia alimentar e rinite&#46; Usou&#8208;se o question&#225;rio ISAAC&#44; validado para nossa linguagem&#44;<a class="elsevierStyleCrossRefs" href="#bib0170"><span class="elsevierStyleSup">14&#44;15</span></a> para avaliar a presen&#231;a de asma e rinite&#46; Al&#233;m disso&#44; foi feita an&#225;lise da gravidade da DA pelo <span class="elsevierStyleItalic">Scoring Atopic Dermatitis</span> &#40;SCORAD&#41;&#46; Os n&#237;veis de gravidade da DA foram definidos como&#59; leve&#44; SCORAD at&#233;&#160;25&#160;pontos&#59; moderado&#44; entre&#160;25&#8211;50&#160;pontos&#59; e grave&#44; acima de&#160;50&#160;pontos&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">16</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Ap&#243;s a assinatura de termos de consentimento&#44; que relataram os principais objetivos&#44; riscos e benef&#237;cios da pesquisa&#44; por parte dos respons&#225;veis e de assentimento por parte dos pacientes adolescentes&#44; amostras de sangue venoso foram coletadas em tubos contendo EDTA&#46; A fim de aumentar a confiabilidade do estudo em rela&#231;&#227;o &#224; an&#225;lise das muta&#231;&#245;es&#44; foram analisadas amostras controle&#46; Devido &#224; dificuldade &#233;tica de criar um grupo controle pedi&#225;trico com coleta de sangue&#44; optou&#8208;se por amostras de um mesmo grupo populacional provenientes de um banco de medula &#243;ssea&#44; as quais foram pareadas por sexo e etnia&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Para a determina&#231;&#227;o da varia&#231;&#227;o gen&#233;tica da filagrina&#160;2&#44; o DNA gen&#244;mico dos indiv&#237;duos participantes do estudo foi purificado com aux&#237;lio do kit QIAamp DNA Blood Mini kit &#40;Qiagen&#44; Valencia&#44; CA&#41;&#44; de acordo com as instru&#231;&#245;es do fabricante&#46; O princ&#237;pio desse kit baseia&#8208;se na extra&#231;&#227;o de DNA gen&#244;mico de c&#233;lulas sangu&#237;neas nucleadas e posterior liga&#231;&#227;o do DNA a uma matriz de fibra de vidro contida em uma coluna de MicroSpin&#46; Resumidamente&#44; ap&#243;s a digest&#227;o das membranas celulares pela proteinase&#160;K&#44; o material nucleico foi transferido para uma membrana de s&#237;lica&#44; onde sofreu v&#225;rias lavagens com solu&#231;&#245;es alco&#243;licas&#46; A elui&#231;&#227;o foi feita pela adi&#231;&#227;o de &#225;gua ultrapura&#46; O DNA gen&#244;mico foi quantificado atrav&#233;s da medida da absorb&#226;ncia na densidade &#243;ptica de 260&#160;nm &#40;OD260&#41; com o espectrofot&#244;metro NanoDrop Lite &#40;<span class="elsevierStyleItalic">ThermoScientific</span>&#41;&#46; A prepara&#231;&#227;o final foi armazenada a &#8208;20<span class="elsevierStyleHsp" style=""></span>&#176;C&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">A genotipagem do gene da filagrina&#160;2 &#40;rs&#160;16833974 e rs&#160;12568784&#41; foi feita atrav&#233;s de PCR em tempo real&#44; usou&#8208;se sonda TaqMan&#174; de uso comercial &#40;ABI assay&#59; <span class="elsevierStyleItalic">Applied Biosystems</span>&#41; marcada com os fluoroforos VIC e FAM para cada alelo&#44; sendo C&#95;34256909&#95;10 para rs16833974 e C&#95;11261511 para rs12568784&#46; Resumidamente&#44; a rea&#231;&#227;o foi feita em um volume final de 10&#160;uL&#44; com 40&#160;ng de DNA gen&#244;mico&#44; Taqman SNP GenotypingAssays 40X e TaqmanGenotyping Master Mix&#44; de acordo com as instru&#231;&#245;es do fabricante&#46; Inicialmente as amostras foram submetidas a uma etapa de leitura pr&#233;&#8208;PCR a 60<span class="elsevierStyleHsp" style=""></span>&#176;C por 30&#160;segundos&#44; seguida pela etapa de desnatura&#231;&#227;o a 95<span class="elsevierStyleHsp" style=""></span>&#176;C durante 10&#160;minutos&#46; Em seguida foram submetidas &#224; etapa de amplifica&#231;&#227;o&#44; que consistia em 40&#160;ciclos de 95<span class="elsevierStyleHsp" style=""></span>&#176;C por 15&#160;segundos e 60<span class="elsevierStyleHsp" style=""></span>&#176;C por 1&#160;minuto&#44; para anelamento do <span class="elsevierStyleItalic">primer</span> e extens&#227;o dos fragmentos&#46; Ap&#243;s a amplifica&#231;&#227;o dos fragmentos de DNA&#44; as amostras foram submetidas &#224; etapa final de leitura p&#243;s&#8208;PCR a 60<span class="elsevierStyleHsp" style=""></span>&#176;C durante 30 segundos&#46; A rea&#231;&#227;o da PCR foi feita com aux&#237;lio do termociclador ABI StepOnePlus Real&#8208;Time PCR System &#40;Applied Biosystems&#44; Foster City&#44; CA&#41;&#46; Os resultados da an&#225;lise de discrimina&#231;&#227;o al&#233;lica foram plotados em um gr&#225;fico de dispers&#227;o que contrastou a fluoresc&#234;ncia de cada sonda&#46;</p><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">An&#225;lise estat&#237;stica</span><p id="par0075" class="elsevierStylePara elsevierViewall">Usou&#8208;se uma amostra de 48&#160;pacientes com um grupo controle maior &#40;1&#44;7&#160;vez&#41; de 83&#160;pacientes&#44; para uma melhor an&#225;lise estat&#237;stica&#46; Fez&#8208;se uso das estat&#237;sticas de frequ&#234;ncia&#44; frequ&#234;ncia relativa e teste qui&#8208;quadrado linear para apresenta&#231;&#227;o das vari&#225;veis em tabelas descritivas&#44; com objetivo de compreender o perfil da amostra e tamb&#233;m do controle&#46; Com o intuito de verificar poss&#237;veis associa&#231;&#245;es usou&#8208;se o teste estat&#237;stico qui&#8208;quadrado&#44; ou o exato de Fisher&#44; para identificar evid&#234;ncias que comprovem signific&#226;ncia de determinadas vari&#225;veis em rela&#231;&#227;o &#224; muta&#231;&#227;o gen&#233;tica estudada e n&#237;vel de <span class="elsevierStyleItalic">Scoring Atopic Dermatitis</span> &#40;SCORAD&#41;&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">Usou&#8208;se o n&#237;vel de signific&#226;ncia de&#160;0&#44;05&#59; p&#8208;valor&#160;&#60;&#160;0&#44;05 para avalia&#231;&#227;o das associa&#231;&#245;es entre a vari&#225;vel dependente &#40;muta&#231;&#245;es no gene da filagrina&#160;2&#41; e as demais vari&#225;veis de interesse do estudo&#46; Os programas Microsoft Excel 2010 e Software R&#44; vers&#227;o&#160;3&#46;3&#46;1 &#40;R Core Team 2015&#44; Viena&#44; &#193;ustria&#41;&#44; foram empregados para organiza&#231;&#227;o&#44; cria&#231;&#227;o de tabelas e an&#225;lise estat&#237;stica dos dados&#46; O estudo seguiu os princ&#237;pios da Declara&#231;&#227;o de Helsinki e foi aprovado pelo comit&#234; de &#233;tica sob parecer n&#176;&#160;36934514&#46;9&#46;0000&#46;5259&#46;</p></span></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Resultados</span><p id="par0090" class="elsevierStylePara elsevierViewall">De novembro&#160;de 2015 a fevereiro de&#160;2016 foram coletados os dados de&#160;48&#160;pacientes&#44; 54&#37; do sexo masculino&#46; O grupo controle foi constitu&#237;do por&#160;83&#160;amostras&#46; A preval&#234;ncia total do polimorfismo rs&#160;16833974 no grupo de pacientes &#233;&#160;16&#44;7&#37; &#40;14&#44;6&#37;&#160;heterozigoto e 2&#44;1&#37;&#160;homozigoto&#41; e no controle 15&#44;7&#37;&#160;&#40;heterozigotos&#41;&#46; J&#225; a preval&#234;ncia total do polimorfismo rs&#160;12568784 &#233;&#58;&#160;43&#44;7&#37; dos pacientes &#40;35&#44;4&#37;&#160;heterozigotos e 8&#44;3&#37;&#160;homozigotos&#41; e dos controles 46&#44;9&#37; &#40;37&#44;3&#37;&#160;heterozigoto e 9&#44;6&#37;&#160;homozigoto&#41;&#46; As principais caracter&#237;sticas da amostra e do grupo controle s&#227;o descritas na <a class="elsevierStyleCrossRef" href="#tbl0005">tabela 1</a></p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0095" class="elsevierStylePara elsevierViewall">A distribui&#231;&#227;o do polimorfismo gen&#233;tico de rs&#160;16833974 e rs&#160;12568784 de acordo com as vari&#225;veis sociodemogr&#225;ficas da amostra e do grupo controle &#233; demonstrada respectivamente na <a class="elsevierStyleCrossRef" href="#tbl0010">tabela 2</a>&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">As principais vari&#225;veis estudadas foram&#58; sexo&#44; etnia&#44; SCORAD&#44; hist&#243;ria familiar de atopia e doen&#231;as al&#233;rgicas associadas&#46; Quanto ao polimorfismo rs&#160;16833974&#44; foram encontradas diferen&#231;as estat&#237;sticas quanto &#224; vari&#225;vel etnia&#44; quanto mais escura a cor da pele&#44; maior a chance de se ter o polimorfismo&#44; p&#8208;valor&#160;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>&#160;0&#44;031 &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">tabela 3</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><p id="par0105" class="elsevierStylePara elsevierViewall">Foram encontradas diferen&#231;as estatisticamente significantes&#44; p &#62; 0&#44;05&#44; de acordo com a <a class="elsevierStyleCrossRef" href="#tbl0020">tabela 4</a>&#46;</p><elsevierMultimedia ident="tbl0020"></elsevierMultimedia><p id="par0110" class="elsevierStylePara elsevierViewall">Quanto ao polimorfismo rs12568784&#44; tamb&#233;m foram estudadas as seguintes vari&#225;veis&#58; sexo&#44; etnia&#44; SCORAD&#44; hist&#243;rico familiar de atopia e doen&#231;as al&#233;rgicas associadas &#40;alergia alimentar&#44; asma e rinite&#41; e n&#227;o foi encontrada signific&#226;ncia estat&#237;stica entre as vari&#225;veis&#44; exceto a vari&#225;vel parental&#46; O teste apresentou p&#8208;valor&#160;<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>&#160;0&#44;032&#44; menor do que o n&#237;vel de signific&#226;ncia de&#160;0&#44;05&#160;&#40;5&#37;&#41;&#46; Visto isso&#44; &#233; poss&#237;vel afirmar a exist&#234;ncia de evid&#234;ncias estat&#237;sticas que comprovem alguma rela&#231;&#227;o de causa entre polimorfismo e atopia &#40;Pai&#41;&#46; De acordo com os dados da tabela pode&#8208;se perceber uma redu&#231;&#227;o no polimorfismo rs&#160;12568784 na presen&#231;a de Atopia &#40;Pai&#41; &#40;<a class="elsevierStyleCrossRef" href="#tbl0020">tabela 4</a>&#41;&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">Foram feitos 46&#160;cruzamentos de interesses no total&#44; buscou&#8208;se verificar signific&#226;ncia estat&#237;stica entre polimorfismo e hist&#243;ria familiar&#44; sexo&#44; etnia&#44; gravidade da doen&#231;a&#44; atopia &#40;asma&#44; rinite&#44; alergia familiar&#41; e compara&#231;&#227;o com o controle quanto &#224; frequ&#234;ncia da muta&#231;&#227;o&#44; etnia e sexo&#46; Buscamos fazer avalia&#231;&#227;o separadamente dos polimorfismos heterozigotos e homozigotos&#44; por&#233;m nenhuma associa&#231;&#227;o foi encontrada&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Discuss&#227;o</span><p id="par0125" class="elsevierStylePara elsevierViewall">A rela&#231;&#227;o entre polimorfismos do gene da filagrina&#160;2 e dermatite at&#243;pica foi recentemente relatada&#46;<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">11</span></a> De acordo com a literatura&#44; o polimorfismo da filagrina&#160;2 pode influenciar a gravidade do quadro&#46;<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">11</span></a> Neste estudo&#44; buscamos analisar alguns pontos dessa associa&#231;&#227;o de forma ampla&#44; atrav&#233;s da an&#225;lise explorat&#243;ria e correla&#231;&#227;o de dados cl&#237;nicos e demogr&#225;ficos&#46;</p><p id="par0130" class="elsevierStylePara elsevierViewall">&#201; importante considerar que o grupo controle usado no estudo foi de conveni&#234;ncia&#44; com amostras de banco de medula &#243;ssea&#44; visto a dificuldade de organizar um grupo controle de crian&#231;as&#46; Foi feito pareamento de sexo e etnia entre os grupos&#46; Este &#233; o primeiro trabalho que usa controles para avaliar polimorfismos da filagrina&#160;2 e DA&#46; N&#227;o foram encontradas diferen&#231;as estat&#237;sticas entre a preval&#234;ncia dos polimorfismos no grupo de pacientes com DA e no grupo controle&#46; Al&#233;m disso&#44; tamb&#233;m n&#227;o houve diferen&#231;a quanto ao n&#237;vel de gravidade em pacientes portadores do polimorfismo&#46;</p><p id="par0135" class="elsevierStylePara elsevierViewall">Da mesma forma&#44; quando se analisaram as correla&#231;&#245;es entre a idade no in&#237;cio da DA e os polimorfismos&#44; n&#227;o houve diferen&#231;as estat&#237;sticas&#46; Assim como descrito por Margolis et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">12</span></a> tamb&#233;m n&#227;o foi encontrada associa&#231;&#227;o do polimorfismo com outros doen&#231;as at&#243;picas avaliadas &#40;asma&#44; rinite&#44; alergia alimentar&#41;&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">A hist&#243;ria familiar &#233; um importante fator de risco para o desenvolvimento da DA&#46; Aproximadamente&#160;70&#37; dos pacientes com DA apresentam hist&#243;ria familiar de doen&#231;as at&#243;picas&#46; A probabilidade de desenvolvimento da DA &#233; de cerca de duas a tr&#234;s vezes maior em crian&#231;as com um dos pais at&#243;picos e aumenta para tr&#234;s a cinco vezes se ambos os pais forem at&#243;picos&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">17</span></a> De um modo geral&#44; a hist&#243;ria materna de DA &#233; mais preditiva para o desenvolvimento de DA em rela&#231;&#227;o &#224; atopia paterna&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">18</span></a> Em nosso estudo&#44;&#160;85&#37; dos pacientes apresentaram hist&#243;ria familiar positiva para atopia&#44; corroboraram a literatura&#46;</p><p id="par0145" class="elsevierStylePara elsevierViewall">De um modo geral&#44; n&#227;o foram observadas diferen&#231;as estat&#237;sticas entre hist&#243;ria familiar de atopia e polimorfismos de filagrina&#160;2&#44; exceto para aumento da frequ&#234;ncia da muta&#231;&#227;o do polimorfismo rs&#160;12568784 na presen&#231;a de atopia paterna&#46; Esse dado pode referir&#8208;se apenas a um achado estat&#237;stico&#44; em fun&#231;&#227;o do reduzido n&#250;mero amostral e possivelmente sem plausibilidade biol&#243;gica&#46; Mais estudos s&#227;o necess&#225;rios para elucidar esse achado&#46;</p><p id="par0150" class="elsevierStylePara elsevierViewall">De acordo com Margolis et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">12</span></a> os polimorfismos do gene da filagrina&#160;2&#44; rs&#160;12568784 e rs&#160;16833974&#44; est&#227;o associadas com a persist&#234;ncia da DA em negros e est&#227;o ausentes&#44; ou s&#227;o raramente encontrados&#44; em indiv&#237;duos de origem europeia&#46; Na popula&#231;&#227;o do estudo&#44; houve signific&#226;ncia estat&#237;stica entre o polimorfismo rs&#160;16833974 e os pacientes com DA autodeclarados negros&#44; o que corroborou a literatura&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">A popula&#231;&#227;o brasileira tem um alto grau de miscigena&#231;&#227;o e segue diferentes padr&#245;es &#233;tnicos quando comparada a grupos populacionais de outros pa&#237;ses e continentes&#44; como China&#44; Estados Unidos&#44; Jap&#227;o e Europa&#44; onde j&#225; existem estudos com preval&#234;ncia da filagrina&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">5</span></a> Portanto&#44; &#233; dif&#237;cil estabelecer uma classifica&#231;&#227;o por etnias em nosso pa&#237;s&#46; O uso exclusivo de informa&#231;&#245;es da etnia autodeclarada n&#227;o &#233; o melhor m&#233;todo para&#160;classi&#64257;ca&#231;&#227;o &#233;tnica<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">19</span></a> e &#233; uma limita&#231;&#227;o do estudo&#46;</p><p id="par0160" class="elsevierStylePara elsevierViewall">Os genomas da maioria dos brasileiros s&#227;o miscigenados e os marcadores gen&#233;ticos s&#227;o capazes de fornecer novos e valiosos <span class="elsevierStyleItalic">insights</span> sobre a estrutura atual da popula&#231;&#227;o brasileira&#46;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">19</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">Perspectivas futuras de an&#225;lises de ancestralidade das amostras sangu&#237;neas de nosso estudo poder&#227;o permitir um melhor esclarecimento acerca da associa&#231;&#227;o entre a filagrina&#160;2 e DA&#44; visto que a preval&#234;ncia das muta&#231;&#245;es do gene da filagrina apresenta diferen&#231;as &#233;tnicas tanto na popula&#231;&#227;o geral quanto em indiv&#237;duos portadores de DA&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">20</span></a></p><p id="par0170" class="elsevierStylePara elsevierViewall">O pequeno tamanho amostral pode ter limitado a signific&#226;ncia de nossos resultados e talvez uma maior amostra e&#47;ou o estudo de ancestralidade poder&#225; contribuir para o esclarecimento entre indiv&#237;duos com DA e os polimorfismo da filagrina&#160;2&#46; A feitura do estudo prote&#244;mico da filagrina&#160;2&#44; j&#225; que diferen&#231;as estruturais podem se dever a controles p&#243;s&#8208;transcricionais&#44; tamb&#233;m contribuiria para uma melhor avalia&#231;&#227;o da filagrina&#160;2&#46;</p><p id="par0175" class="elsevierStylePara elsevierViewall">At&#233; o momento&#44; n&#227;o h&#225; estudos de polimorfismos do gene da filagrina&#160;2 e DA na Am&#233;rica Latina&#44; o que refor&#231;ando a relev&#226;ncia de nosso estudo e o ineditismo dessa iniciativa no Brasil&#46; Al&#233;m disso&#44; este &#233; o primeiro estudo em n&#237;vel mundial que usa um grupo controle para avaliar altera&#231;&#245;es no gene da filagrina&#160;2&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Conclus&#227;o</span><p id="par0185" class="elsevierStylePara elsevierViewall">Muito pouco se sabe sobre o perfil de polimorfismos de filagrinas&#160;2 associados &#224; DA na altamente miscigenada popula&#231;&#227;o brasileira&#46; Os resultados deste trabalho podem ser um consider&#225;vel incentivo &#224;s pesquisas sobre polimorfismos e DA no pa&#237;s&#44; colaborar para uma melhor compreens&#227;o&#44; n&#227;o apenas de formas de tratamento da doen&#231;a&#44; mas tamb&#233;m do perfil gen&#233;tico da popula&#231;&#227;o&#46;</p><p id="par0190" class="elsevierStylePara elsevierViewall">Quanto ao polimorfismo rs16833974&#44; foram encontradas diferen&#231;as estatisticamente significantes em rela&#231;&#227;o &#224; vari&#225;vel etnia&#46; Quanto mais escura a cor da pele&#44; maior a chance de ocorrer o polimorfismo&#44; valor de p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;031&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Suporte financeiro</span><p id="par0200" class="elsevierStylePara elsevierViewall">Fundo de Apoio &#224; Dermatologia &#40;Funaderm&#41;&#44; da Sociedade Brasileira de Dermatologia&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Contribui&#231;&#227;o dos autores</span><p id="par0210" class="elsevierStylePara elsevierViewall">Amanda Hertz&#58; Concep&#231;&#227;o e planejamento do estudo&#59; obten&#231;&#227;o&#44; an&#225;lise e interpreta&#231;&#227;o dos dados&#59; revis&#227;o cr&#237;tica da literatura&#46;</p><p id="par0215" class="elsevierStylePara elsevierViewall">Luna Azulay&#8208;Abulafia&#58; Participa&#231;&#227;o efetiva na orienta&#231;&#227;o da pesquisa&#46;</p><p id="par0220" class="elsevierStylePara elsevierViewall">Adriana Paulino do Nascimento&#58; Concep&#231;&#227;o e planejamento do estudo&#59; obten&#231;&#227;o&#44; an&#225;lise e interpreta&#231;&#227;o dos dados&#46;</p><p id="par0225" class="elsevierStylePara elsevierViewall">Cintya Yumi Ohara&#58; Concep&#231;&#227;o e planejamento do estudo&#46;</p><p id="par0230" class="elsevierStylePara elsevierViewall">Fabio Chigres Kuschnir&#58; Revis&#227;o cr&#237;tica da literatura&#59; revis&#227;o cr&#237;tica do manuscrito&#46;</p><p id="par0235" class="elsevierStylePara elsevierViewall">Lu&#237;s Cristov&#227;o Porto&#58; Concep&#231;&#227;o e planejamento do estudo&#59; obten&#231;&#227;o&#44; an&#225;lise e interpreta&#231;&#227;o dos dados&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Conflitos de interesse</span><p id="par0245" class="elsevierStylePara elsevierViewall">Nenhum&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Fundamentos</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Polimorfismos do gene da filagrina&#160;2 &#40;rs&#160;12568784 e rs&#160;16899374&#41; est&#227;o associados com dermatite at&#243;pica persistente em pacientes negros&#46; A filagrina&#160;2 &#233; uma prote&#237;na com fun&#231;&#227;o semelhante &#224; filagrina e tamb&#233;m codificada no complexo de diferencia&#231;&#227;o da epiderme no cromossomo 1q21&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Objetivo</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Avaliar os polimorfismos no gene da filagrina&#160;2 &#40;rs&#160;12568784 e rs&#160;16899374&#41; em crian&#231;as e adultos com dermatite at&#243;pica e verificar a associa&#231;&#227;o desses com a gravidade do quadro cl&#237;nico&#44; presen&#231;a de outras doen&#231;as al&#233;rgicas e fatores sociodemogr&#225;ficos&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">M&#233;todo</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">O estudo foi feito com pacientes do ambulat&#243;rio de dermatite at&#243;pica e grupo controle&#46; Foram usados question&#225;rios para avaliar etnia&#44; sexo&#44; faixa et&#225;ria&#44; hist&#243;rico familiar&#44; <span class="elsevierStyleItalic">Scoring</span><span class="elsevierStyleItalic">Atopic Dermatitis</span> &#40;SCORAD&#41;&#44; entre outros par&#226;metros&#46; A genotipagem do gene da filagrina&#160;2 foi feita atrav&#233;s de rea&#231;&#227;o em cadeia da polimerase em tempo real&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Resultados</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Foram avaliados&#160;48&#160;pacientes e 83&#160;controles&#46; N&#227;o foi encontrada uma correla&#231;&#227;o entre as vari&#225;veis estudadas dos pacientes com dermatite at&#243;pica e os polimorfismos&#46; Tamb&#233;m n&#227;o houve diferen&#231;a significativa entre a preval&#234;ncia dos polimorfismos nos pacientes e no grupo controle p&#160;&#62;&#160;0&#44;05&#46;</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Limita&#231;&#245;es do estudo</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">O uso exclusivo de informa&#231;&#245;es da etnia autodeclarada e o n&#250;mero da amostra&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Resultados</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Os resultados deste trabalho podem ser um incentivo para o estudo de polimorfismos na dermatite at&#243;pica&#44; considerando&#8208;se a caracter&#237;stica multi&#233;tnica da popula&#231;&#227;o brasileira&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conclus&#227;o</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Este &#233; um trabalho in&#233;dito no Brasil e o primeiro estudo no mundo a ter um grupo controle para avaliar altera&#231;&#245;es no gene da filagrina&#160;2&#46;</p></span>"
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">35&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pardos&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">12&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">25&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">26&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">31&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#44;51&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pretos&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">18&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">38&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">28&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">34&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o identificado&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">2&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " colspan="7" align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " colspan="7" align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">Idade</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Infanto &#40;0&#8211;2 anos&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">8&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">21&#8211;30 anos&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">55&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">66&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Crian&#231;as &#40;3&#8211;9 anos&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">28&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">58&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">31&#8211;45 anos&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">21&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">25&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Adolescentes &#40;10&#8211;19 anos&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">13&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">27&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&#62; 45 anos&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">7&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Adultos &#40;20&#160;anos ou mais&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">6&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">N&#227;o identificado&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">1&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
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        "etiqueta" => "Tabela 2"
        "tipo" => "MULTIMEDIATABLA"
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            "detalle" => "Tabela "
            "rol" => "short"
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                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td-with-role" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">Vari&#225;veis sociodemogr&#225;ficas&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="10" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Polimorfismo rs16833974</th></tr><tr title="table-row"><th class="td" title="\n
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                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="5" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Pacientes</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="5" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Controle</th></tr><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="2" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Presente</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="2" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Ausente</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">p&#8208;valor&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="2" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Presente</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " colspan="2" align="center" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Ausente</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">p&#8208;valor&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">n&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">n&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
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            1 => array:2 [
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                  \t\t\t\t" scope="col">Vari&#225;veis sociodemogr&#225;ficas&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col">Vari&#225;veis estudadas&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Polimorfismo rs 16833974</th><th class="td" title="\n
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                  \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n
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                  \t\t\t\t  " colspan="8" align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o identificado&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Alergia alimentar</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t" scope="col">Vari&#225;veis estudadas&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Polimorfismo rs12568784</th><th class="td" title="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o identificado&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o identificado&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Alergia alimentar</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N&#227;o&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">7&#37;&nbsp;\t\t\t\t\t\t\n
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Vol. 95. Núm. 2.
Páginas 173-179 (1 março 2020)
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Vol. 95. Núm. 2.
Páginas 173-179 (1 março 2020)
Investigação
Open Access
Análise dos polimorfismos no gene da filagrina 2 em pacientes com dermatite atópica
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Amanda Hertza,
Autor para correspondência
hertzamanda@gmail.com

Autor para correspondência.
, Luna Azulay‐Abulafiab, Adriana Paulino do Nascimentoc, Cintya Yumi Oharad, Fabio Chigres Kuschnire,f, Luís Cristovão Portoc
a Ambulatório de Dermatologia Pediátrica, Instituto de Dermatologia Prof. Rubem David Azulay, Rio de Janeiro, RJ, Brasil
b Departamento de Dermatologia, Instituto de Dermatologia Prof. Rubem David Azulay, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
c Laboratório de Histocompatibilidade e Criopreservação, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
d Departamento de Alergia e Imunopatologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
e Departamento de Pediatria, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
f Departamento de Alergia, Universidade Estadual do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
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Estatísticas
Tabelas (4)
Tabela 1. Distribuição dos dados sociodemográficos dos pacientes e controles
Tabela 2. Distribuição do polimorfismo rs16833974 e rs12568784 de acordo com as variáveis sociodemográficas da amostra e do grupo controle
Tabela 3. Variáveis estudadas na amostra e polimorfismo rs16833974
Tabela 4. Variáveis estudadas na amostra e polimorfismo rs1256878
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Resumo
Fundamentos

Polimorfismos do gene da filagrina 2 (rs 12568784 e rs 16899374) estão associados com dermatite atópica persistente em pacientes negros. A filagrina 2 é uma proteína com função semelhante à filagrina e também codificada no complexo de diferenciação da epiderme no cromossomo 1q21.

Objetivo

Avaliar os polimorfismos no gene da filagrina 2 (rs 12568784 e rs 16899374) em crianças e adultos com dermatite atópica e verificar a associação desses com a gravidade do quadro clínico, presença de outras doenças alérgicas e fatores sociodemográficos.

Método

O estudo foi feito com pacientes do ambulatório de dermatite atópica e grupo controle. Foram usados questionários para avaliar etnia, sexo, faixa etária, histórico familiar, ScoringAtopic Dermatitis (SCORAD), entre outros parâmetros. A genotipagem do gene da filagrina 2 foi feita através de reação em cadeia da polimerase em tempo real.

Resultados

Foram avaliados 48 pacientes e 83 controles. Não foi encontrada uma correlação entre as variáveis estudadas dos pacientes com dermatite atópica e os polimorfismos. Também não houve diferença significativa entre a prevalência dos polimorfismos nos pacientes e no grupo controle p > 0,05.

Limitações do estudo

O uso exclusivo de informações da etnia autodeclarada e o número da amostra.

Resultados

Os resultados deste trabalho podem ser um incentivo para o estudo de polimorfismos na dermatite atópica, considerando‐se a característica multiétnica da população brasileira.

Conclusão

Este é um trabalho inédito no Brasil e o primeiro estudo no mundo a ter um grupo controle para avaliar alterações no gene da filagrina 2.

Palavras‐chave:
Alergia
Dermatite atópica
Imunologia
Polimorfismo genético
Texto Completo
Introdução

A dermatite atópica (DA) é uma doença inflamatória da pele frequente e que afeta aproximadamente 20% das crianças, compromete a qualidade de vida do paciente e da família. Mutações no gene que codifica a proteína epidérmica filagrina demonstram ser um fator importante para o desenvolvimento dessa doença.1 A filagrina também está associada com a persistência e coexistência de outras doenças alérgicas.2

A filagrina (FILAGGRIN: FILamentAGGRegatingproteIN) é uma proteína encontrada nos corneócitos responsável por agregar a queratina na formação do estrato córneo.3 É produzida a partir de um precursor, a pró‐filagrina, que se localiza na camada granulosa da epiderme nos grânulos de querato hialina. A pró‐filagrina é subsequentemente desfosforilada, resulta na formação de monómeros de filagrina que têm propriedades de agregação de filamentos de queratina. A degradação da filagrina gera os fatores de hidratação natural (Natural Mosturizing Factors − NMFs), que incluem aminoácidos livres, ácido urocânico (UCA) e ácido pirrolidônico carboxílico (PCA). Os NMFs promovem captação e aprisionamento da água e manutenção do pH ácido da pele, essencial para o processo de hidratação e manutenção da barreira cutânea.4

O gene que codifica a filagrina está localizado no cromossomo 1q21, em uma região denominada complexo de diferenciação epidérmica.3 De acordo com a literatura; 27,5% dos brancos americanos; 48% dos europeus; 31,4% dos chineses e 20% dos japoneses portadores de dermatite atópica apresentam mutações no gene da filagrina.5

Atualmente 47 mutações com perda de função já foram identificadas no gene que codifica a filagrina em pacientes com DA. Perfis distintos de mutações foram identificados em pacientes da Europa e da Ásia.6 Entre as mutações descritas, as mais comumente encontradas nos brancos são a R501X e a 2282del4 (compreendem 50% do total), além da R2447X e da S3247X.7 Na população japonesa, as principais mutações foram a 3321delA e a S2554X.8 Essas mutações parecem variar de acordo com grupos étnicos, por exemplo, na população negra estudos demonstraram uma prevalência bem menor que nos brancos.9 Gao et al.10 encontraram a R501X em 3,2% [U1] de 187 pacientes negros com dermatite atópica e nenhuma associação com 2282del4. Já Margolis et al.7 avaliaram o genótipo de 370 negros com DA e encontraram mutações em apenas 1% dos pacientes8 (R501X 3,2%; 2282del4 0,5%; S3247X 3% e R2447X 1,4%).

A filagrina 2 é uma proteína com função semelhante à filagrina e também codificada na região denominada complexo de diferenciação da epiderme. De acordo com Makino et al.,11 a expressão da proteína filagrina 2 está diminuída em portadores de DA. Há relato de uma associação entre polimorfismos no gene da filagrina 2 (rs 12568784 e rs 1689937411) e DA persistente em pacientes negros portadores de dermatite atópica.12

Não há estudos sobre a prevalência de filagrina e filagrina 2 na população brasileira. O objetivo deste estudo foi avaliar os polimorfismos no gene da filagrina 2 (rs 12568784 e rs 16899374) em crianças e adultos com dermatite atópica e verificar a associação desses com a gravidade do quadro clínico, presença de outras doenças alérgicas e fatores sociodemográficos.

Métodos

Estudo transversal, envolveu pacientes de ambos os sexos, entre um e 27 anos, com diagnóstico de dermatite atópica, de acordo com os critérios da United Kingdom Working Party (UK),13 recrutados nos ambulatórios de dermatite atópica. Foram excluídos aqueles com outras doenças crônicas da pele (psoríase, entre outras) ou doenças sistêmicas que afetam a pele, como imunodeficiências primárias, lúpus eritematoso sistêmico, entre outras.

De acordo com a ordem de chegada ao ambulatório, os pacientes responderam a um questionário com as seguintes variáveis: sexo, idade, etnia, início da DA, história familiar de doenças alérgicas e presença de asma, alergia alimentar e rinite. Usou‐se o questionário ISAAC, validado para nossa linguagem,14,15 para avaliar a presença de asma e rinite. Além disso, foi feita análise da gravidade da DA pelo Scoring Atopic Dermatitis (SCORAD). Os níveis de gravidade da DA foram definidos como; leve, SCORAD até 25 pontos; moderado, entre 25–50 pontos; e grave, acima de 50 pontos.16

Após a assinatura de termos de consentimento, que relataram os principais objetivos, riscos e benefícios da pesquisa, por parte dos responsáveis e de assentimento por parte dos pacientes adolescentes, amostras de sangue venoso foram coletadas em tubos contendo EDTA. A fim de aumentar a confiabilidade do estudo em relação à análise das mutações, foram analisadas amostras controle. Devido à dificuldade ética de criar um grupo controle pediátrico com coleta de sangue, optou‐se por amostras de um mesmo grupo populacional provenientes de um banco de medula óssea, as quais foram pareadas por sexo e etnia.

Para a determinação da variação genética da filagrina 2, o DNA genômico dos indivíduos participantes do estudo foi purificado com auxílio do kit QIAamp DNA Blood Mini kit (Qiagen, Valencia, CA), de acordo com as instruções do fabricante. O princípio desse kit baseia‐se na extração de DNA genômico de células sanguíneas nucleadas e posterior ligação do DNA a uma matriz de fibra de vidro contida em uma coluna de MicroSpin. Resumidamente, após a digestão das membranas celulares pela proteinase K, o material nucleico foi transferido para uma membrana de sílica, onde sofreu várias lavagens com soluções alcoólicas. A eluição foi feita pela adição de água ultrapura. O DNA genômico foi quantificado através da medida da absorbância na densidade óptica de 260 nm (OD260) com o espectrofotômetro NanoDrop Lite (ThermoScientific). A preparação final foi armazenada a ‐20°C.

A genotipagem do gene da filagrina 2 (rs 16833974 e rs 12568784) foi feita através de PCR em tempo real, usou‐se sonda TaqMan® de uso comercial (ABI assay; Applied Biosystems) marcada com os fluoroforos VIC e FAM para cada alelo, sendo C_34256909_10 para rs16833974 e C_11261511 para rs12568784. Resumidamente, a reação foi feita em um volume final de 10 uL, com 40 ng de DNA genômico, Taqman SNP GenotypingAssays 40X e TaqmanGenotyping Master Mix, de acordo com as instruções do fabricante. Inicialmente as amostras foram submetidas a uma etapa de leitura pré‐PCR a 60°C por 30 segundos, seguida pela etapa de desnaturação a 95°C durante 10 minutos. Em seguida foram submetidas à etapa de amplificação, que consistia em 40 ciclos de 95°C por 15 segundos e 60°C por 1 minuto, para anelamento do primer e extensão dos fragmentos. Após a amplificação dos fragmentos de DNA, as amostras foram submetidas à etapa final de leitura pós‐PCR a 60°C durante 30 segundos. A reação da PCR foi feita com auxílio do termociclador ABI StepOnePlus Real‐Time PCR System (Applied Biosystems, Foster City, CA). Os resultados da análise de discriminação alélica foram plotados em um gráfico de dispersão que contrastou a fluorescência de cada sonda.

Análise estatística

Usou‐se uma amostra de 48 pacientes com um grupo controle maior (1,7 vez) de 83 pacientes, para uma melhor análise estatística. Fez‐se uso das estatísticas de frequência, frequência relativa e teste qui‐quadrado linear para apresentação das variáveis em tabelas descritivas, com objetivo de compreender o perfil da amostra e também do controle. Com o intuito de verificar possíveis associações usou‐se o teste estatístico qui‐quadrado, ou o exato de Fisher, para identificar evidências que comprovem significância de determinadas variáveis em relação à mutação genética estudada e nível de Scoring Atopic Dermatitis (SCORAD).

Usou‐se o nível de significância de 0,05; p‐valor < 0,05 para avaliação das associações entre a variável dependente (mutações no gene da filagrina 2) e as demais variáveis de interesse do estudo. Os programas Microsoft Excel 2010 e Software R, versão 3.3.1 (R Core Team 2015, Viena, Áustria), foram empregados para organização, criação de tabelas e análise estatística dos dados. O estudo seguiu os princípios da Declaração de Helsinki e foi aprovado pelo comitê de ética sob parecer n° 36934514.9.0000.5259.

Resultados

De novembro de 2015 a fevereiro de 2016 foram coletados os dados de 48 pacientes, 54% do sexo masculino. O grupo controle foi constituído por 83 amostras. A prevalência total do polimorfismo rs 16833974 no grupo de pacientes é 16,7% (14,6% heterozigoto e 2,1% homozigoto) e no controle 15,7% (heterozigotos). Já a prevalência total do polimorfismo rs 12568784 é: 43,7% dos pacientes (35,4% heterozigotos e 8,3% homozigotos) e dos controles 46,9% (37,3% heterozigoto e 9,6% homozigoto). As principais características da amostra e do grupo controle são descritas na tabela 1

Tabela 1.

Distribuição dos dados sociodemográficos dos pacientes e controles

Variáveis sociodemográficas  PacientesControle
     
Sexo
22  46%    33  40%  0,58 
26  54%    50  60%   
Etnia
Brancos  17  35%    29  35%   
Pardos  12  25%    26  31%  0,51 
Pretos  18  38%    28  34%   
Não identificado  2%    0%   
Idade
Infanto (0–2 anos)  8%  21–30 anos  55  66%   
Crianças (3–9 anos)  28  58%  31–45 anos  21  25%   
Adolescentes (10–19 anos)  13  27%  > 45 anos  7%   
Adultos (20 anos ou mais)  6%  Não identificado  1%   

A distribuição do polimorfismo genético de rs 16833974 e rs 12568784 de acordo com as variáveis sociodemográficas da amostra e do grupo controle é demonstrada respectivamente na tabela 2.

Tabela 2.

Distribuição do polimorfismo rs16833974 e rs12568784 de acordo com as variáveis sociodemográficas da amostra e do grupo controle

Variáveis sociodemográficas  Polimorfismo rs16833974
  PacientesControle
  PresenteAusentep‐valor  PresenteAusentep‐valor 
     
Sexo
8%  18  38%  6%  28  34%  0,14 
8%  22  46%    10%  42  51%   
Etnia
Brancos  2%  16  33%  0,08  1%  28  34%  0,03 
Pardos  2%  11  23%    5%  22  27%   
Pretos  13%  12  25%    10%  20  24%   
Não identificado  0%  2%    0%  0%   
Variáveis sociodemográficas  Polimorfismo rs12568784
  PacientesControle
  PresenteAusentep‐valor  PresenteAusentep‐valor 
     
Sexo
11  23%  11  23%  0,56  19  23%  14  17%  0,17 
10  21%  16  33%    20  24%  30  36%   
Etnia
Brancos  15%  10  21%  0,38  10  12%  19  23%  0,51 
Pardos  6%  19%    17  20%  11%   
Pretos  10  21%  17%    12  14%  16  19%   
Não identificado  2%  0%    0%  0%   

As principais variáveis estudadas foram: sexo, etnia, SCORAD, história familiar de atopia e doenças alérgicas associadas. Quanto ao polimorfismo rs 16833974, foram encontradas diferenças estatísticas quanto à variável etnia, quanto mais escura a cor da pele, maior a chance de se ter o polimorfismo, p‐valor = 0,031 (tabela 3).

Tabela 3.

Variáveis estudadas na amostra e polimorfismo rs16833974

Variáveis estudadas  Polimorfismo rs 16833974Totalp‐valor 
  PresenteAusente 
       
Sexo
50%  18  45%  22  46%   
50%  22  55%  26  54%   
Total  100%  40  100%  48  100%   
Scorad
Leve  75%  13  33%  19  40%  0,026 
Moderado  25%  15  38%  17  35%   
Grave  0%  10  25%  10  21%   
Não identificado  0%  5%  4%   
Total  100%  40  100%  48  100%   
HF Atopia
Sim  100%  33  83%  41  85%  0,56 
Não  0%  13%  10%   
Não identificado  0%  5%  4%   
Total  100%  40  100%  48  100%   
Mãe
Sim  63%  18  45%  23  48%  0,7 
Não  38%  17  43%  20  42%   
Não identificado  0%  13%  10%   
Total  100%  40  100%  48  100%   
Pai
Sim  75%  16  40%  22  46%  0,24 
Não  25%  19  48%  21  44%   
Não identificado  0%  13%  10%   
Total  100%  40  100%  48  100%   
Etnia
Brancos  13%  16  40%  17  35%  0,031 
Pardos  13%  11  28%  12  25%   
Pretos  75%  12  30%  18  38%   
Não identificado  0%  3%  2%   
Total  100%  40  100%  48  100%   
Asma
Sim  50%  18  45%  22  46%  0,66 
Não  25%  19  48%  21  44%   
Não identificado  25%  8%  10%   
Total  100%  40  100%  48  100%   
Alergia alimentar
Sim  13%  15  38%  16  33%  0,37 
Não  63%  22  55%  27  56%   

Foram encontradas diferenças estatisticamente significantes, p > 0,05, de acordo com a tabela 4.

Tabela 4.

Variáveis estudadas na amostra e polimorfismo rs1256878

Variáveis estudadas  Polimorfismo rs12568784Totalp‐valor 
  PresenteAusente 
       
Sexo
11  52%  11  41%  22  46%  0,56 
10  48%  16  59%  26  54%   
Total  21  100%  27  100%  48  100%   
Scorad
Leve  43%  10  37%  19  40%  0,91 
Moderado  24%  12  44%  17  35%   
Grave  24%  19%  10  21%   
Não identificado  10%  0%  4%   
Total  21  100%  27  100%  48  100%   
HF atopia
Sim  20  95%  21  78%  41  85%  0,059 
Não  0%  19%  10%   
Não identificado  5%  4%  4%   
Total  21  100%  27  100%  48  100%   
Mãe
Sim  11  52%  12  44%  23  48%  1,00 
Não  43%  11  41%  20  42%   
Não identificado  5%  15%  10%   
Total  21  100%  27  100%  48  100%   
Pai
Sim  14  67%  30%  22  46%  0,032 
Não  29%  15  56%  21  44%   
Não identificado  5%  15%  10%   
Total  21  100%  27  100%  48  100%   
Etnia
Brancos  33%  10  37%  17  35%  0,38 
Pardos  14%  33%  12  25%   
Pretos  10  48%  30%  18  38%   
Não identificado  5%  0%  2%   
Total  21  100%  27  100%  48  100%   
Asma
Sim  38%  14  52%  22  46%  0,54 
Não  10  48%  11  41%  21  44%   
Não identificado  14%  7%  10%   
Total  21  100%  27  100%  48  100%   
Alergia alimentar
Sim  29%  10  37%  16  33%  0,75 
Não  12  57%  15  56%  27  56%   
Não identificado  14%  7%  10%   
Total  21  100%  27  100%  48  100%   

Quanto ao polimorfismo rs12568784, também foram estudadas as seguintes variáveis: sexo, etnia, SCORAD, histórico familiar de atopia e doenças alérgicas associadas (alergia alimentar, asma e rinite) e não foi encontrada significância estatística entre as variáveis, exceto a variável parental. O teste apresentou p‐valor = 0,032, menor do que o nível de significância de 0,05 (5%). Visto isso, é possível afirmar a existência de evidências estatísticas que comprovem alguma relação de causa entre polimorfismo e atopia (Pai). De acordo com os dados da tabela pode‐se perceber uma redução no polimorfismo rs 12568784 na presença de Atopia (Pai) (tabela 4).

Foram feitos 46 cruzamentos de interesses no total, buscou‐se verificar significância estatística entre polimorfismo e história familiar, sexo, etnia, gravidade da doença, atopia (asma, rinite, alergia familiar) e comparação com o controle quanto à frequência da mutação, etnia e sexo. Buscamos fazer avaliação separadamente dos polimorfismos heterozigotos e homozigotos, porém nenhuma associação foi encontrada.

Discussão

A relação entre polimorfismos do gene da filagrina 2 e dermatite atópica foi recentemente relatada.11 De acordo com a literatura, o polimorfismo da filagrina 2 pode influenciar a gravidade do quadro.11 Neste estudo, buscamos analisar alguns pontos dessa associação de forma ampla, através da análise exploratória e correlação de dados clínicos e demográficos.

É importante considerar que o grupo controle usado no estudo foi de conveniência, com amostras de banco de medula óssea, visto a dificuldade de organizar um grupo controle de crianças. Foi feito pareamento de sexo e etnia entre os grupos. Este é o primeiro trabalho que usa controles para avaliar polimorfismos da filagrina 2 e DA. Não foram encontradas diferenças estatísticas entre a prevalência dos polimorfismos no grupo de pacientes com DA e no grupo controle. Além disso, também não houve diferença quanto ao nível de gravidade em pacientes portadores do polimorfismo.

Da mesma forma, quando se analisaram as correlações entre a idade no início da DA e os polimorfismos, não houve diferenças estatísticas. Assim como descrito por Margolis et al.,12 também não foi encontrada associação do polimorfismo com outros doenças atópicas avaliadas (asma, rinite, alergia alimentar).

A história familiar é um importante fator de risco para o desenvolvimento da DA. Aproximadamente 70% dos pacientes com DA apresentam história familiar de doenças atópicas. A probabilidade de desenvolvimento da DA é de cerca de duas a três vezes maior em crianças com um dos pais atópicos e aumenta para três a cinco vezes se ambos os pais forem atópicos.17 De um modo geral, a história materna de DA é mais preditiva para o desenvolvimento de DA em relação à atopia paterna.18 Em nosso estudo, 85% dos pacientes apresentaram história familiar positiva para atopia, corroboraram a literatura.

De um modo geral, não foram observadas diferenças estatísticas entre história familiar de atopia e polimorfismos de filagrina 2, exceto para aumento da frequência da mutação do polimorfismo rs 12568784 na presença de atopia paterna. Esse dado pode referir‐se apenas a um achado estatístico, em função do reduzido número amostral e possivelmente sem plausibilidade biológica. Mais estudos são necessários para elucidar esse achado.

De acordo com Margolis et al.,12 os polimorfismos do gene da filagrina 2, rs 12568784 e rs 16833974, estão associadas com a persistência da DA em negros e estão ausentes, ou são raramente encontrados, em indivíduos de origem europeia. Na população do estudo, houve significância estatística entre o polimorfismo rs 16833974 e os pacientes com DA autodeclarados negros, o que corroborou a literatura.

A população brasileira tem um alto grau de miscigenação e segue diferentes padrões étnicos quando comparada a grupos populacionais de outros países e continentes, como China, Estados Unidos, Japão e Europa, onde já existem estudos com prevalência da filagrina.5 Portanto, é difícil estabelecer uma classificação por etnias em nosso país. O uso exclusivo de informações da etnia autodeclarada não é o melhor método para classificação étnica19 e é uma limitação do estudo.

Os genomas da maioria dos brasileiros são miscigenados e os marcadores genéticos são capazes de fornecer novos e valiosos insights sobre a estrutura atual da população brasileira.19

Perspectivas futuras de análises de ancestralidade das amostras sanguíneas de nosso estudo poderão permitir um melhor esclarecimento acerca da associação entre a filagrina 2 e DA, visto que a prevalência das mutações do gene da filagrina apresenta diferenças étnicas tanto na população geral quanto em indivíduos portadores de DA.20

O pequeno tamanho amostral pode ter limitado a significância de nossos resultados e talvez uma maior amostra e/ou o estudo de ancestralidade poderá contribuir para o esclarecimento entre indivíduos com DA e os polimorfismo da filagrina 2. A feitura do estudo proteômico da filagrina 2, já que diferenças estruturais podem se dever a controles pós‐transcricionais, também contribuiria para uma melhor avaliação da filagrina 2.

Até o momento, não há estudos de polimorfismos do gene da filagrina 2 e DA na América Latina, o que reforçando a relevância de nosso estudo e o ineditismo dessa iniciativa no Brasil. Além disso, este é o primeiro estudo em nível mundial que usa um grupo controle para avaliar alterações no gene da filagrina 2.

Conclusão

Muito pouco se sabe sobre o perfil de polimorfismos de filagrinas 2 associados à DA na altamente miscigenada população brasileira. Os resultados deste trabalho podem ser um considerável incentivo às pesquisas sobre polimorfismos e DA no país, colaborar para uma melhor compreensão, não apenas de formas de tratamento da doença, mas também do perfil genético da população.

Quanto ao polimorfismo rs16833974, foram encontradas diferenças estatisticamente significantes em relação à variável etnia. Quanto mais escura a cor da pele, maior a chance de ocorrer o polimorfismo, valor de p=0,031.

Suporte financeiro

Fundo de Apoio à Dermatologia (Funaderm), da Sociedade Brasileira de Dermatologia.

Contribuição dos autores

Amanda Hertz: Concepção e planejamento do estudo; obtenção, análise e interpretação dos dados; revisão crítica da literatura.

Luna Azulay‐Abulafia: Participação efetiva na orientação da pesquisa.

Adriana Paulino do Nascimento: Concepção e planejamento do estudo; obtenção, análise e interpretação dos dados.

Cintya Yumi Ohara: Concepção e planejamento do estudo.

Fabio Chigres Kuschnir: Revisão crítica da literatura; revisão crítica do manuscrito.

Luís Cristovão Porto: Concepção e planejamento do estudo; obtenção, análise e interpretação dos dados.

Conflitos de interesse

Nenhum.

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Como citar este artigo: Hertz A, Azulay‐Abulafia L, Nascimento AP, Ohara CY, Kuschnir FC, Porto LC. Analysis of filaggrin 2 gene polymorphisms in patients with atopic dermatitis. An Bras Dermatol. 2020;95:173–179.

Trabalho realizado no Ambulatório de Dermatite Atópica, Policlínica Piquet Carneiro, Universidade do Estado do Rio de Janeiro, RJ, Brasil.

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