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Association of FOXP3 gene polymorphism in Chinese women with endometriosis / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 106-110, 2013.
Artigo em Chinês | WPRIM | ID: wpr-232193
ABSTRACT
<p><b>OBJECTIVE</b>To assess the association between single nucleotide polymorphisms (SNPs) of forkhead box P3 gene (FOXP3) and endometriosis in Chinese Han women from central China.</p><p><b>METHODS</b>MassARRAY IPLEX and matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) technique was used to determine the genotypes of FOXP3 gene in 314 patients with endometriosis and 358 healthy controls.</p><p><b>RESULTS</b>Genotypes of C/T polymorphism for the rs2280883 locus, A/C for the rs3761548 locus, and C/T for the rs3761549 locus were determined. No significant difference was detected in distribution of genotypes CC, CT and TT (P=0.770, OR=0.960; P=0.923, OR=1.013) and frequencies of C and T alleles (P=0.772, OR=0.960; P=0.925, OR=1.013) for rs2280883 and rs3761549 between the two groups. And no significant difference was detected in distribution of genotypes AA, AC and CC (P=0.762, OR=0.958) and frequencies of A and C alleles (P=0.715, OR=0.950) for rs3761548 was detected between the two groups. Based on r-AFS classification, the patients were divided into two groups (respectively with I-II stage and III-IV stage endometriosis). Again, no significant difference was detected in distribution of genotypes CC, CT and TT (P=0.454, OR=1.198, P=0.526, OR=0.909; P=0.220, OR=0.750, P=0.548, OR=1.094) and frequencies of C and T alleles (P=0.473, OR=1.215, P=0.532, OR=0.912; P=0.204, OR=0.737, P=0.558, OR=1.089) for rs22080883 and rs3761549 loci between the two patient groups. No association was found between distribution of genotypes AA, AC and CC (P=0.431, OR=1.211; P=0.508, OR=0.905) and frequencies of A and C alleles (P=0.417, OR=1.226; P=0.516, OR=0.908) for rs3761548 locus between the two patient groups.</p><p><b>CONCLUSION</b>Our study has failed to found any association between FOXP3 gene polymorphisms rs2280883, rs3761548 and rs3761549 with endometriosis in Chinese Han patients.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Estudos de Casos e Controles / China / Estudos Retrospectivos / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / Endometriose / Alelos / Fatores de Transcrição Forkhead / Frequência do Gene Tipo de estudo: Estudo observacional / Fatores de risco Limite: Adolescente / Adulto / Feminino / Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2013 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Estudos de Casos e Controles / China / Estudos Retrospectivos / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / Endometriose / Alelos / Fatores de Transcrição Forkhead / Frequência do Gene Tipo de estudo: Estudo observacional / Fatores de risco Limite: Adolescente / Adulto / Feminino / Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2013 Tipo de documento: Artigo