Zhang F, Zhai G, Kato B S, Hart D J, Hunter D, Spector T D, Ahmadi K R
Twin Research and Genetic Epidemiology Unit, King's College London, St. Thomas' Hospital Campus, London, UK.
Osteoarthritis Cartilage. 2007 Jun;15(6):624-9. doi: 10.1016/j.joca.2006.12.002. Epub 2007 Jan 30.
Osteoarthritis (OA) is a common complex disease with strong heritable components. In this study, we investigated the association between four putatively functional genetic variants in KLOTHO gene, a strong ageing-related gene, and hand OA in a large female Caucasian population.
Subjects (n=1015, age range 33-74 years) were selected from the TwinsUK Registry. Radiographs of both hands were taken for each individual with standard posteroanterior view. The presence/absence of radiographic OA, osteophyte and joint space narrowing (JSN) was assessed using a standard atlas. Four putatively functional single nucleotide polymorphisms (SNPs) in KLOTHO gene were genotyped using allelic discrimination assay. Association was initially estimated using Pearson's chi(2) or Fisher's exact test at allelic and genotypic levels. The direction and magnitude of significant association were further investigated by robust logistic regression with age as a covariate.
We found significant association between SNP G-395A and the presence/absence of radiographic hand OA and osteophyte, but not JSN. Allele G significantly increased the risk for radiographic hand OA and osteophytes with odds ratios (ORs) of 1.44 (P=0.008, 95% confidence interval (CI) 1.09-1.91) and 1.36 (P=0.006, 95% CI 1.09-1.70), respectively. From logistic regression modelling, genotype GG showed more than three-fold increased risk for both radiographic hand OA (OR=3.10, 95% CI 1.10-8.76) and osteophyte (OR=3.10, 95% CI 1.10-8.75) when compared to genotype AA. After adjustment for age, ORs for genotype GG further increased to 4.39 (P=0.006, 95% CI 1.51-12.74) for radiographic hand OA and to 4.47 (P=0.005, 95% CI 1.56-12.77) for osteophytes.
Our results suggest that one variant in KLOTHO gene is associated with the susceptibility of hand OA and appears to act through osteophyte formation rather than cartilage damage.
骨关节炎(OA)是一种常见的复杂疾病,具有很强的遗传成分。在本研究中,我们调查了与衰老密切相关的KLOTHO基因中四个可能具有功能的基因变异与一大群白人女性手部骨关节炎之间的关联。
从英国双胞胎登记处选取受试者(n = 1015,年龄范围33 - 74岁)。为每位个体拍摄双手的标准后前位X线片。使用标准图谱评估X线片上骨关节炎、骨赘和关节间隙变窄(JSN)的有无。采用等位基因鉴别分析对KLOTHO基因中的四个可能具有功能的单核苷酸多态性(SNP)进行基因分型。最初在等位基因和基因型水平上使用Pearson卡方检验或Fisher精确检验估计关联性。通过以年龄作为协变量的稳健逻辑回归进一步研究显著关联的方向和程度。
我们发现SNP G - 395A与手部X线片骨关节炎和骨赘的有无之间存在显著关联,但与JSN无关。等位基因G显著增加了手部X线片骨关节炎和骨赘的风险,优势比(OR)分别为1.44(P = 0.008,95%置信区间(CI)1.09 - 1.91)和1.36(P = 0.006,95% CI 1.09 - 1.70)。根据逻辑回归模型,与基因型AA相比,基因型GG在手部X线片骨关节炎(OR = 3.10,95% CI 1.10 - 8.76)和骨赘(OR = 3.10,95% CI 1.10 - 8.75)方面显示出超过三倍的风险增加。在调整年龄后,基因型GG在手部X线片骨关节炎方面的OR进一步增加到4.39(P = 0.006,95% CI 1.51 - 12.74),在骨赘方面增加到4.47(P = 0.005,95% CI 1.56 - 12.77)。
我们的数据表明,KLOTHO基因中的一个变异与手部骨关节炎的易感性相关,并且似乎是通过骨赘形成而非软骨损伤起作用。