Yazdi Masoud Mahdinezhad, Jamalaldini Mohamad H, Sobhan Mohammad R, Jafari Mohammadali, Mazaheri Mahta, Zare-Shehneh Masoud, Neamatzadeh Hossein
Department of Orthopedics, Afshar Hospital, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Arch Bone Jt Surg. 2017 Nov;5(6):351-362.
Many studies have reported the association of estrogen receptor α gene (ESRα) ESRα PvuII T>C, XbaI A>G and BtgI G>A polymorphisms with Knee osteoarthritis (KOA) risk, but the results remained controversial. In order to drive a more precise estimation, the present systematic review and meta-analysis was performed to investigate the association between ESRα polymorphisms and KOA susceptibility.
Eligible articles were identified by search of databases including PubMed, ISI Web of Knowledge and Google scholar up to March 1, 2017. Data were extracted by two independent authors and pooled odds ratio (OR) with 95% confidence interval (CI) was calculated.
A total of 22 case-control studies in eleven publications with 6,575 KOA cases and 7,459 controls were included in the meta-analysis. By pooling all the studies, either ESRα PvuII T>C and XbaI A>G polymorphisms was not associated with KOA risk in the overall population. However, ESRα BtgI G>A was significantly associated with KOA risk under all five genetic models. In the subgroup analysis by ethnicity, a significant association was observed between ESRα PvuII T>C polymorphism and KOA risk in Asians under heterozygote model. In addition, significant association was found between ESRα XbaI A>G polymorphism and KOA in Caucasians under allelic, homozygote, dominant and recessive models.
The present meta-analysis suggests that ESRα BtgI G>A rather than ESRα PvuII T>C and XbaI A>G polymorphisms is associated with an increased KOA risk in overall population. Moreover, we have found that ESRα PvuII T>C and XbaI A>G polymorphisms associated with KOA susceptibility by ethnicity backgrounds.
许多研究报道了雌激素受体α基因(ESRα)的ESRα PvuII T>C、XbaI A>G和BtgI G>A多态性与膝关节骨关节炎(KOA)风险的关联,但结果仍存在争议。为了进行更精确的评估,本系统评价和荟萃分析旨在研究ESRα多态性与KOA易感性之间的关联。
通过检索包括PubMed、ISI Web of Knowledge和谷歌学术在内的数据库,确定截至2017年3月1日的符合条件的文章。由两名独立作者提取数据,并计算合并比值比(OR)及95%置信区间(CI)。
荟萃分析共纳入了11篇出版物中的22项病例对照研究,包括6575例KOA病例和7459例对照。汇总所有研究后,ESRα PvuII T>C和XbaI A>G多态性在总体人群中均与KOA风险无关。然而,ESRα BtgI G>A在所有五种遗传模型下均与KOA风险显著相关。在按种族进行的亚组分析中,在杂合子模型下,亚洲人中ESRα PvuII T>C多态性与KOA风险之间存在显著关联。此外,在等位基因、纯合子、显性和隐性模型下,白种人中ESRα XbaI A>G多态性与KOA之间存在显著关联。
本荟萃分析表明,ESRα BtgI G>A而非ESRα PvuII T>C和XbaI A>G多态性与总体人群中KOA风险增加相关。此外,我们发现ESRα PvuII T>C和XbaI A>G多态性与KOA易感性存在种族背景相关性。