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与血清25-羟维生素D水平相关的GC基因多态性是日本类风湿性关节炎患者髋部骨折的危险因素:风湿病研究所类风湿性关节炎队列研究的10年随访

A GC polymorphism associated with serum 25-hydroxyvitamin D level is a risk factor for hip fracture in Japanese patients with rheumatoid arthritis: 10-year follow-up of the Institute of Rheumatology, Rheumatoid Arthritis cohort study.

作者信息

Yoshida Shinji, Ikari Katsunori, Furuya Takefumi, Toyama Yoshiaki, Taniguchi Atsuo, Yamanaka Hisashi, Momohara Shigeki

出版信息

Arthritis Res Ther. 2014 Mar 20;16(2):R75. doi: 10.1186/ar4516.

Abstract

INTRODUCTION

Vitamin D deficiency has been reported to be common in patients with rheumatoid arthritis (RA) who have a higher prevalence of osteoporosis and hip fracture than healthy individuals. Genetic variants affecting serum 25-hydroxyvitamin D (25(OH)D) concentration, an indicator of vitamin D status, were recently identified by genome-wide association studies of Caucasian populations. The purpose of this study was to validate the association and to test whether the serum 25(OH)D-linked genetic variants were associated with the occurrence of hip fracture in Japanese RA patients.

METHODS

DNA samples of 1,957 Japanese RA patients were obtained from the Institute of Rheumatology, Rheumatoid Arthritis (IORRA) cohort DNA collection. First, five single nucleotide polymorphisms (SNPs) that were reported to be associated with serum 25(OH)D concentration by genome-wide association studies were genotyped. The SNPs that showed a significant association with serum 25(OH)D level in the cross-sectional study were used in the longitudinal analysis of hip fracture risk. The genetic risk for hip fracture was determined by a multivariate Cox proportional hazards model in 1,957 patients with a maximum follow-up of 10 years (median, 8 years).

RESULTS

Multivariate linear regression analyses showed that rs2282679 in GC (the gene encoding group-specific component (vitamin D binding protein)) locus was significantly associated with lower serum 25(OH)D concentration (P = 8.1 × 10⁻⁵). A Cox proportional hazards model indicated that rs2282679 in GC was significantly associated with the occurrence of hip fracture in a recessive model (hazard ratio (95% confidence interval) = 2.52 (1.05-6.05), P = 0.039).

CONCLUSIONS

A two-staged analysis demonstrated that rs2282679 in GC was associated with serum 25(OH)D concentration and could be a risk factor for hip fracture in Japanese RA patients.

摘要

引言

据报道,类风湿关节炎(RA)患者中维生素D缺乏症很常见,这些患者骨质疏松症和髋部骨折的患病率高于健康个体。全基因组关联研究最近在白种人群体中鉴定出了影响血清25-羟基维生素D(25(OH)D)浓度(维生素D状态的一个指标)的基因变异。本研究的目的是验证这种关联,并测试血清25(OH)D相关基因变异是否与日本RA患者髋部骨折的发生有关。

方法

从类风湿关节炎研究所(IORRA)队列DNA库中获取了1957名日本RA患者的DNA样本。首先,对全基因组关联研究中报道的与血清25(OH)D浓度相关的五个单核苷酸多态性(SNP)进行基因分型。在横断面研究中与血清25(OH)D水平显示出显著关联的SNP被用于髋部骨折风险的纵向分析。通过多变量Cox比例风险模型在1957名患者中确定髋部骨折的遗传风险,最长随访时间为10年(中位数为8年)。

结果

多变量线性回归分析显示,GC(编码组特异性成分(维生素D结合蛋白)的基因)位点中的rs2282679与较低的血清25(OH)D浓度显著相关(P = 8.1×10⁻⁵)。Cox比例风险模型表明,GC中的rs2282679在隐性模型中与髋部骨折的发生显著相关(风险比(95%置信区间)= 2.52(1.05 - 6.05),P = 0.039)。

结论

两阶段分析表明,GC中的rs2282679与血清25(OH)D浓度相关,并且可能是日本RA患者髋部骨折的一个风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1b/4060202/5c6f30cb21ec/ar4516-1.jpg

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