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首页> 外文期刊>British Journal of Dermatology >Association study between keratinocyte-derived growth factor gene polymorphisms and susceptibility to vitiligo vulgaris in a Taiwanese population: potential involvement of stem cell factor.
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Association study between keratinocyte-derived growth factor gene polymorphisms and susceptibility to vitiligo vulgaris in a Taiwanese population: potential involvement of stem cell factor.

机译:台湾人群中角质形成细胞衍生的生长因子基因多态性与寻常型白癜风易感性的关联研究:干细胞因子的潜在参与。

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摘要

BACKGROUND: Vitiligo vulgaris is a depigmentary disorder resulting from the disappearance of functional melanocytes. Currently, the pathogenesis of this disorder remains obscure. OBJECTIVES: Genetic analysis of patients with vitilgo may provide important clues for elucidating the complex pathomechanisms involved in the disease process. Because dysfunctional keratinocytes have recently been implicated in the pathogenesis of vitiligo vulgaris, we conducted a case-control association study to investigate this phenomenon. PATIENTS AND METHODS: Fifty-one patients with vitiligo vulgaris and 118 healthy controls from Taiwan were recruited to investigate the association between relevant keratinocyte-related genes and the occurrence of vitiligo vulgaris. This study genotyped 11 single-nucleotide polymorphisms (SNPs) in five genes including stem cell factor (SCF, also known as KITLG), basic fibroblast growth factor (bFGF, also known as NuDT6), endothelin-1 (EDN1), hepatocyte growth factor (HGF) and stem cell growth factor (SCGF, also known as CLEC11A). RESULTS: Our results revealed that the A allele for SNP rs11104947 in the SCF gene and the T allele for SNP rs13866 in the SCGF gene were, respectively, associated with a 1.95- and a 2.14-fold risk of developing vitiligo vulgaris. A higher risk was also detected among subjects who carried the SCF rs995029/rs11104947 C/A haplotype (odds ratio = 2.45). Furthermore, the at-risk alleles for SCF rs11104947 (A allele) and for SCGF SNP rs13866 (T allele) were found to display a 7.92-fold increased gene-gene combined risk. No significant relationship between polymorphic frequency for genes bFGF, EDN1 as well as HGF and occurrence of vitiligo vulgaris was observed. CONCLUSIONS: These novel genetic findings provide new insights in relation to the mechanisms that might be involved in the development of vitiligo vulgaris.
机译:背景:寻常性白癜风是由功能性黑素细胞消失引起的色素沉着症。目前,这种疾病的发病机理仍然不清楚。目的:白癜风患者的遗传分析可能为阐明疾病过程中涉及的复杂发病机制提供重要线索。由于功能紊乱的角质形成细胞最近与寻常型白癜风的发病有关,我们进行了病例对照关联研究以研究这种现象。病人和方法:招募了来自台湾的51名寻常型白癜风患者和118名健康对照者,研究相关的角质形成细胞相关基因与寻常型白癜风的发生之间的关系。这项研究对五个基因中的11个单核苷酸多态性(SNP)进行了基因分型,包括干细胞因子(SCF,也称为KITLG),碱性成纤维细胞生长因子(bFGF,也称为NuDT6),内皮素-1(EDN1),肝细胞生长因子(HGF)和干细胞生长因子(SCGF,也称为CLEC11A)。结果:我们的结果显示,SCF基因中SNP rs11104947的A等位基因和SCGF基因中SNP rs13866的T等位基因分别与寻常型白癜风发生风险的1.95和2.14倍相关。在携带SCF rs995029 / rs11104947 C / A单倍型的受试者中也检测到较高的风险(优势比= 2.45)。此外,发现SCF rs11104947(A等位基因)和SCGF SNP rs13866(T等位基因)的高风险等位基因显示基因-基因组合风险增加了7.92倍。没有观察到基因bFGF,EDN1和HGF的多态性频率与寻常性白癜风的发生之间存在显着关系。结论:这些新颖的遗传发现为寻常寻常性白癜风的发展可能涉及的机制提供了新的见解。

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