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TRAF6 基因变异与类风湿关节炎患者的低骨密度相关。

A TRAF6 genetic variant is associated with low bone mineral density in rheumatoid arthritis.

机构信息

Laboratory of Immunology, Research Unit UR 807, Faculty of Medicine of Sousse, Ibn Al Jazzar street, 4000, Sousse, Tunisia.

Department of Rheumatology, Farhat Hached Hospital, Sousse, Tunisia.

出版信息

Clin Rheumatol. 2019 Apr;38(4):1067-1074. doi: 10.1007/s10067-018-4362-1. Epub 2018 Dec 1.

Abstract

OBJECTIVES

This study was aimed to investigate the association of the single nucleotide polymorphism of tumor necrosis factor receptor associated factor 6 (TRAF6), rs540386, with low bone mineral density (BMD) among patients with rheumatoid arthritis (RA).

METHODS

TRAF6 rs540386 genotyping was performed by mutagenically separated PCR in a cohort of 188 (23 men, 165 women, median age, 56.2 years) adult RA patients and 224 age and gender-matched controls. BMD was measured using dual-energy X-ray absorptiometry (DXA) (Lunar Prodigy advance scans, GE Healthcare, USA).

RESULTS

Among the RA patients, 64 (55 women, 9 men) had low BMD comprising of 57 patients with osteoporosis and 7 with osteopenia. Whereas TRAF6 rs540386 was not associated with RA susceptibility, it was however found to be a risk factor for reduced lumbar spine Z-score in the recessive model (OR = 3.34, 95% CI = (1.01-11.00), p = 0.038). This association was confirmed further in the multivariate logistic regression analysis taking into account several potential confounding factors (OR = 3.34 (1.01-11.00), p = 0.048). In addition, mean total femur Z-score was found to be reduced in TT patients when compared to CC + CT patients (- 1.30 ± 1.32 versus - 0.60 ± 1.05, p = 0.034). No association between TRAF6 rs540386 and local bone damage was observed.

CONCLUSIONS

This study for the first time ever demonstrated an association between a genetic variant of TRAF6 and low BMD among patients with RA. Further investigations are needed to elucidate the exact role of this variant.

摘要

目的

本研究旨在探讨肿瘤坏死因子受体相关因子 6(TRAF6)单核苷酸多态性 rs540386 与类风湿关节炎(RA)患者低骨密度(BMD)之间的关联。

方法

采用突变分离 PCR 法对 188 例(男 23 例,女 165 例,中位年龄 56.2 岁)成年 RA 患者和 224 名年龄和性别匹配的对照者进行 TRAF6 rs540386 基因分型。采用双能 X 线吸收法(DXA)(Lunar Prodigy advance 扫描,GE Healthcare,美国)测量 BMD。

结果

在 RA 患者中,64 例(55 例女性,9 例男性)存在低 BMD,包括 57 例骨质疏松症患者和 7 例骨量减少症患者。虽然 TRAF6 rs540386 与 RA 易感性无关,但在隐性模型中发现其是腰椎 Z 评分降低的危险因素(OR=3.34,95%CI=(1.01-11.00),p=0.038)。在考虑了几个潜在混杂因素的多变量逻辑回归分析中,进一步证实了这种关联(OR=3.34(1.01-11.00),p=0.048)。此外,与 CC+CT 患者相比,TT 患者的总股骨 Z 评分均值降低(-1.30±1.32 与-0.60±1.05,p=0.034)。未观察到 TRAF6 rs540386 与局部骨损伤之间的关联。

结论

本研究首次证明 TRAF6 基因变异与 RA 患者的低 BMD 之间存在关联。需要进一步的研究来阐明该变异的确切作用。

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