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雌激素受体-α基因PvuII和XbaI多态性与骨关节炎风险的关联:一项荟萃分析。

Association between estrogen receptor-alpha gene PvuII and XbaI polymorphisms and osteoarthritis risk: a meta-analysis.

作者信息

Hu Wei, Shuang Feng, Zou Hong-Xing, Yang Huai-He

机构信息

Department of Orthopedics, The 94th Hospital of Chinese PLA Nanchang 330002, China.

出版信息

Int J Clin Exp Med. 2015 Feb 15;8(2):1956-65. eCollection 2015.

Abstract

Estrogen receptor-alpha (ER-α) gene PvuII (T/C) and XbaI (A/G) polymorphisms have been hypothesized to be associated with osteoarthritis (OA) risk by several epidemiological studies, however, the available results were inconclusive and conflicting. We conducted a meta-analysis of 10 case-control studies that included 3328 osteoarthritis cases and 6390 case-free controls. We assessed the strength of the association, using odds ratios (ORs) with 95% confidence intervals (CIs). This meta-analysis showed that the ER-α PvuII and XbaI polymorphisms were not associated with OA risk in overall population. For the PvuII (T/C) polymorphism, however, in the subgroup analysis by country, a significantly reduced risk was observed among Chinese (TC vs. CC: OR = 0.73, 95% CI 0.54-0.99, I (2) = 0%, P heterogeneity = 0.498; dominant model, OR = 0.73, 95% CI = 0.55-0.98, I (2) = 0%, P heterogeneity = 0.555). For the XbaI (A/G) polymorphism, when stratifying by sample size, a significantly elevated risk was found in sample size ≤ 500 (AA vs. GG: OR = 2.60, 95% CI 1.10-6.18, I (2) = 42.9%, P heterogeneity = 0.135; dominant model: OR = 2.04, 95% CI 1.12-3.71, I (2) = 11.4%, P heterogeneity = 0.341; and recessive model: OR = 1.69, 95% CI 1.12-2.55, I (2) = 40.2%, P heterogeneity = 0.154). No publication bias was found in the present study. This meta-analysis suggests that ER-α PvuII (T/C) polymorphism may be associated with a reduced OA risk among Chinese and the XbaI (A/G) polymorphism may not be associated with OA risk, while the observed increase in OA risk for XbaI polymorphism may be due to small-study bias.

摘要

多项流行病学研究推测,雌激素受体α(ER-α)基因PvuII(T/C)和XbaI(A/G)多态性可能与骨关节炎(OA)风险相关,但现有结果尚无定论且相互矛盾。我们对10项病例对照研究进行了荟萃分析,这些研究纳入了3328例骨关节炎病例和6390例无病对照。我们使用比值比(OR)及95%置信区间(CI)评估关联强度。该荟萃分析表明,ER-α PvuII和XbaI多态性与总体人群的OA风险无关。然而,对于PvuII(T/C)多态性,在按国家进行的亚组分析中,中国人群的风险显著降低(TC与CC相比:OR = 0.73,95% CI 0.54 - 0.99,I² = 0%,P异质性 = 0.498;显性模型,OR = 0.73,95% CI = 0.55 - 0.98,I² = 0%,P异质性 = 0.555)。对于XbaI(A/G)多态性,按样本量分层时,样本量≤500的研究中风险显著升高(AA与GG相比:OR = 2.60,95% CI 1.10 - 6.18,I² = 42.9%,P异质性 = 0.135;显性模型:OR = 2.04,95% CI 1.12 - 3.71,I² = 11.4%,P异质性 = 0.341;隐性模型:OR = 1.69,95% CI 1.12 - 2.55,I² = 40.2%,P异质性 = 0.154)。本研究未发现发表偏倚。该荟萃分析表明,ER-α PvuII(T/C)多态性可能与中国人群OA风险降低相关,而XbaI(A/G)多态性可能与OA风险无关,XbaI多态性观察到的OA风险增加可能是由于小样本研究偏倚所致。

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