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Association between KLOTHO gene and hand osteoarthritis in a female Caucasian population.

机译:女性白人人群中KLOTHO基因与手部骨关节炎之间的关联。

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OBJECTIVE: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
机译:目的:骨关节炎(OA)是一种常见的复杂疾病,具有很强的遗传力。在这项研究中,我们调查了大量女性高加索人口中KLOTHO基因(一个与衰老相关的基因)中的四个推定功能性遗传变异与手OA之间的关联。方法:从TwinsUK注册表中选择受试者(n = 1015,年龄范围33-74岁)。用标准后后视图为每个人拍摄双手X射线照片。使用标准图谱评估是否存在放射学OA,骨赘和关节间隙变窄(JSN)。使用等位基因鉴别分析对KLOTHO基因中的四个假定功能性单核苷酸多态性(SNP)进行基因分型。最初使用等位基因和基因型水平的Pearson's chi(2)或Fisher精确检验估计关联。通过将年龄作为协变量的稳健逻辑回归分析,进一步研究了显着关联的方向和幅度。结果:我们发现SNP G-395A与放射手OA和骨赘的存在/不存在显着相关,而JSN则不存在。等位基因G显着增加了X线照相手OA和骨赘的风险,优势比(OR)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) , 分别。根据逻辑回归模型,基因型GG与基因型相比显示放射手OA(OR = 3.10,95%CI 1.10-8.76)和骨赘(OR = 3.10,95%CI 1.10-8.75)的风险增加了三倍以上。机管局。调整年龄后,基因型GG的ORs对于放射照相手OA进一步增加到4.39(P = 0.006,95%CI 1.51-12.74),而对于骨赘则增加到4.47(P = 0.005,95%CI 1.56-12.77)。结论:我们的结果表明,KLOTHO基因的一种变异与手OA的易感性有关,并且似乎通过骨赘形成而不是软骨损伤起作用。

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