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尝试在一个大型、明确的骨关节炎病例对照人群(GOAL 研究)中复制已发表的遗传关联。

Attempt to replicate published genetic associations in a large, well-defined osteoarthritis case-control population (the GOAL study).

机构信息

Department of Public Health and Epidemiology, Nottingham University Medical School, Nottingham NG7 2UH, UK.

出版信息

Osteoarthritis Cartilage. 2009 Jun;17(6):782-9. doi: 10.1016/j.joca.2008.09.019. Epub 2008 Nov 1.

DOI:10.1016/j.joca.2008.09.019
PMID:19036616
Abstract

OBJECTIVE

Published studies have tested over 90 genes for association with osteoarthritis (OA), but few positives reported have been independently replicated. Using a new case-control study, our aim was to attempt the replication of findings from 12 genes reported to have significant genetic association with OA and to further examine the role of genetic variation in six of these genes.

METHODS

A case-control study was undertaken in Nottingham, UK. Hospital-referred index cases with symptomatic, radiographic OA (ROA) of the knee (n=1040) or hip (n=1004) were recruited. Asymptomatic controls (n=1123) were recruited from intravenous urography waiting lists and screened for radiographic hip and knee OA. Sixty-eight polymorphisms were genotyped in IL1A, IL1B, IL1RN, IL4R, IL6, COL2A1, ADAM12, ASPN, IGF1, TGFB1, ESR1 and VDR. Statistical analysis compared allele or genotype frequencies of these polymorphisms in all asymptomatic controls and the subset of controls without ROA vs all OA, knee OA and hip OA. The analyses were adjusted for age, gender and body mass index.

RESULTS

We were unable to replicate any of the published genetic associations investigated. Our extended exploratory analyses identified some associations between polymorphisms in TGFB1, IGF1 and IL1RN and OA; but the strength of evidence varied with the control group used.

CONCLUSION

Lack of replication is common and could be due to differences in study design, phenotype, populations examined or the occurrence of false positives in the initial study. Variants within TGFB1, IGF1 and IL1RN could have a role in OA susceptibility; however, replication of these findings is required in an independent study.

摘要

目的

已发表的研究已经测试了超过 90 个与骨关节炎(OA)相关的基因,但报告的阳性结果很少得到独立重复。本研究采用新的病例对照研究,旨在尝试复制与 OA 具有显著遗传相关性的 12 个基因的研究结果,并进一步研究其中 6 个基因的遗传变异的作用。

方法

在英国诺丁汉进行了一项病例对照研究。招募了膝关节(n=1040)或髋关节(n=1004)有症状、放射学 OA(ROA)的医院转诊指数病例。无症状对照(n=1123)从静脉尿路造影等候名单中招募,并对髋关节和膝关节 ROA 进行放射学筛查。在 IL1A、IL1B、IL1RN、IL4R、IL6、COL2A1、ADAM12、ASPN、IGF1、TGFB1、ESR1 和 VDR 中检测了 68 个多态性。在所有无症状对照者和无 ROA 的对照者亚组与所有 OA、膝 OA 和髋 OA 之间比较了这些多态性的等位基因或基因型频率。分析调整了年龄、性别和体重指数。

结果

我们无法复制已发表的任何遗传关联研究。我们的扩展探索性分析发现 TGFB1、IGF1 和 IL1RN 中的多态性与 OA 之间存在一些关联;但证据的强度因使用的对照组而异。

结论

缺乏复制是常见的,可能是由于研究设计、表型、研究人群或初始研究中假阳性的发生不同所致。TGFB1、IGF1 和 IL1RN 中的变体可能在 OA 易感性中起作用;然而,需要在独立研究中复制这些发现。

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