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首页> 外文期刊>Rheumatology international. >Genetic polymorphisms of interleukin-1beta (-511C/T) and interleukin-1 receptor antagonist (86-bpVNTR) in susceptibility to knee osteoarthritis in a Chinese Han population.
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Genetic polymorphisms of interleukin-1beta (-511C/T) and interleukin-1 receptor antagonist (86-bpVNTR) in susceptibility to knee osteoarthritis in a Chinese Han population.

机译:白细胞介素-1β(-511C / T)和白介素-1受体拮抗剂(86-bpVNTR)的遗传多态性在中国汉族人群中易患膝骨关节炎。

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摘要

Osteoarthritis (OA) is a multifactorial disorder in which genetic factors act as important contributors to its onset and progression. Associations between genetic polymorphisms of the interleukin-1 (IL-1) gene cluster and OA susceptibility have been studied continuously in different ethnic groups, yielding controversial results. This study investigated the association of interleukin-1beta (-511C/T) and interleukin-1 receptor antagonist (86-bp VNTR) polymorphisms with knee OA susceptibility in a Chinese Han population. A case-control association study was conducted. The two polymorphisms were genotyped in 453 patients who had primary symptomatic knee OA with radiographic confirmation and in 487 matched controls. Allelic and genotypic frequencies and haplotype distribution were compared between OA and control subjects. For either of the two loci, no significant difference was detected in genotype or allele distribution between knee OA and control groups (all P > 0.05). The haplotype distribution of the two loci showed no difference between the two groups, either. Furthermore, no association between the genotype of the -511 and VNTR polymorphisms and the clinical variables, age, sex, body mass index and Kellgren/Lawrence score was observed in OA patients. The genetic polymorphisms of interleukin-1beta and interleukin-1 receptor antagonist are not risk factors for OA etiology in Han Chinese.
机译:骨关节炎(OA)是一种多因素疾病,遗传因素是其发病和进展的重要因素。在不同种族中,对白介素-1(IL-1)基因簇的遗传多态性与OA易感性之间的关联进行了持续研究,得出了有争议的结果。这项研究调查了中国汉族人群白细胞介素-1β(-511C / T)和白细胞介素-1受体拮抗剂(86-bp VNTR)多态性与膝骨OA易感性的关系。进行了病例对照协会研究。这两种多态性在453例经影像学检查证实为原发性症状性膝OA的患者和487名匹配的对照中进行了基因分型。比较了OA和对照对象之间的等位基因和基因型频率以及单倍型分布。对于这两个基因座中的任何一个,膝OA和对照组之间的基因型或等位基因分布均未检测到显着差异(所有P> 0.05)。两个基因座的单倍型分布在两组之间也没有差异。此外,在OA患者中未观察到-511和VNTR基因多态性的基因型与临床变量,年龄,性别,体重指数和Kellgren / Lawrence评分之间的关​​联。 IL-1β和IL-1受体拮抗剂的遗传多态性不是汉族人群OA病因的危险因素。

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