Hospital Clinico Universitario de Santiago, Santiago de Compostela, Spain.
Arthritis Rheumatol. 2014 Apr;66(4):940-9. doi: 10.1002/art.38300.
To assess candidate genes for association with osteoarthritis (OA) and identify promising genetic factors and, secondarily, to assess the candidate gene approach in OA.
A total of 199 candidate genes for association with OA were identified using Human Genome Epidemiology (HuGE) Navigator. All of their single-nucleotide polymorphisms (SNPs) with an allele frequency of >5% were assessed by fixed-effects meta-analysis of 9 genome-wide association studies (GWAS) that included 5,636 patients with knee OA and 16,972 control subjects and 4,349 patients with hip OA and 17,836 control subjects of European ancestry. An additional 5,921 individuals were genotyped for significantly associated SNPs in the meta-analysis. After correction for the number of independent tests, P values less than 1.58 × 10(-5) were considered significant.
SNPs at only 2 of the 199 candidate genes (COL11A1 and VEGF) were associated with OA in the meta-analysis. Two SNPs in COL11A1 showed association with hip OA in the combined analysis: rs4907986 (P = 1.29 × 10(-5) , odds ratio [OR] 1.12, 95% confidence interval [95% CI] 1.06-1.17) and rs1241164 (P = 1.47 × 10(-5) , OR 0.82, 95% CI 0.74-0.89). The sex-stratified analysis also showed association of COL11A1 SNP rs4908291 in women (P = 1.29 × 10(-5) , OR 0.87, 95% CI 0.82-0.92); this SNP showed linkage disequilibrium with rs4907986. A single SNP of VEGF, rs833058, showed association with hip OA in men (P = 1.35 × 10(-5) , OR 0.85, 95% CI 0.79-0.91). After additional samples were genotyped, association at one of the COL11A1 signals was reinforced, whereas association at VEGF was slightly weakened.
Two candidate genes, COL11A1 and VEGF, were significantly associated with OA in this focused meta-analysis. The remaining candidate genes were not associated.
评估与骨关节炎(OA)相关的候选基因,并确定有前途的遗传因素,其次,评估候选基因方法在 OA 中的应用。
使用人类基因组流行病学(HuGE)导航器确定了 199 个与 OA 相关的候选基因。使用固定效应荟萃分析评估了所有具有 >5%等位基因频率的单核苷酸多态性(SNP),该分析纳入了 9 项全基因组关联研究(GWAS),其中包括 5636 名膝关节 OA 患者和 16972 名对照受试者以及 4349 名髋关节 OA 患者和 17836 名欧洲血统对照受试者。对荟萃分析中具有显著相关性的 SNP 进行了另外 5921 名个体的基因分型。经过对独立测试数量的校正,P 值小于 1.58×10(-5)被认为具有统计学意义。
在荟萃分析中,只有 199 个候选基因中的 2 个(COL11A1 和 VEGF)与 OA 相关。COL11A1 中的 2 个 SNP 与髋关节 OA 存在关联:rs4907986(P=1.29×10(-5),OR 1.12,95%置信区间[95%CI]1.06-1.17)和 rs1241164(P=1.47×10(-5),OR 0.82,95%CI 0.74-0.89)。性别分层分析还显示 COL11A1 SNP rs4908291 在女性中存在关联(P=1.29×10(-5),OR 0.87,95%CI 0.82-0.92);该 SNP 与 rs4907986 存在连锁不平衡。VEGF 中的单个 SNP rs833058 与男性髋关节 OA 相关(P=1.35×10(-5),OR 0.85,95%CI 0.79-0.91)。在进一步对样本进行基因分型后,COL11A1 信号之一的关联得到了加强,而 VEGF 的关联则略有减弱。
在本次重点荟萃分析中,有 2 个候选基因 COL11A1 和 VEGF 与 OA 显著相关。其余候选基因没有相关性。