Sobhan Mohammad Reza, Mahdinezhad-Yazdi Masoud, Dastgheib Seyed Alireza, Jafari Mohammadali, Raee-Ezzabadi Ali, Neamatzadeh Hossein
Departamento de Ortopedia, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Departamento de Genética Médica, Faculdade de Medicina, Shiraz University of Medical Sciences, Shiraz, Iran.
Rev Bras Ortop (Sao Paulo). 2020 Feb;55(1):8-16. doi: 10.1016/j.rboe.2018.03.001. Epub 2020 Jan 9.
Several association studies of genes polymorphisms on estrogen receptors-α and β with respect to adolescent idiopathic scoliosis (AIS) have been published in the past two decades. However, the association with AIS, especially among different ethnic subgroups, still remains controversial. Thus, we investigated these inconclusive data by performing a meta-analysis to systematically evaluate the association. A literature search was conducted in the PubMed, ISI Web of Science, EMBASE, SCOPUS, EBSCO, Cochrane Library, China National Knowledge Infrastructure (CNKI) and Wanfang databases until January 20, 2018. The strength of relationship was assessed using odds ratios (ORs) and 95% confidence intervals (95%CIs). A total of 12 case-control studies with 4,304 cases of AIS and 3,123 controls met our criteria. The pooled ORs indicated that the ESRα XbaI A > G, ESRα PvuII T > C and ESRβ AlwNI T > C polymorphisms were not significantly associated with the risk of developing AIS in the overall analysis. However, we found a significant association between the ESRα XbaI A > G polymorphism and AIS under the homozygote model (GG versus AA; OR = 1.448, 95%CI: 1.052-1.993; = 0.023). The present meta-analysis suggests that the ESRα XbaI A > G, ESRα PvuII T > C and ESRβ AlwNI T > C polymorphisms may not be associated with the risk of developing AIS in the overall analysis. However, ESRα XbaI A > G might have an influence on the susceptibility to develop AIS among Asians. Considering the limited sample size and ethnicity, further larger studies are needed to provide a more precise estimation of the associations.
在过去二十年中,已经发表了几项关于雌激素受体-α和-β基因多态性与青少年特发性脊柱侧凸(AIS)的关联研究。然而,与AIS的关联,特别是在不同种族亚组之间,仍然存在争议。因此,我们通过进行荟萃分析来系统评估这种关联,从而研究这些不确定的数据。在PubMed、ISI科学网、EMBASE、SCOPUS、EBSCO、Cochrane图书馆、中国知网(CNKI)和万方数据库中进行了文献检索,直至2018年1月20日。使用优势比(OR)和95%置信区间(95%CI)评估关联强度。共有12项病例对照研究符合我们的标准,其中包括4304例AIS病例和3123例对照。汇总的OR表明,在总体分析中,ESRα XbaI A>G、ESRα PvuII T>C和ESRβ AlwNI T>C多态性与发生AIS的风险没有显著关联。然而,我们发现在纯合子模型下(GG与AA相比;OR=1.448,95%CI:1.052-1.993;P=0.023),ESRα XbaI A>G多态性与AIS之间存在显著关联。本荟萃分析表明,在总体分析中,ESRα XbaI A>G、ESRα PvuII T>C和ESRβ AlwNI T>C多态性可能与发生AIS的风险无关。然而,ESRα XbaI A>G可能对亚洲人发生AIS的易感性有影响。考虑到样本量和种族的局限性,需要进一步开展更大规模的研究,以更精确地估计这些关联。