Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad-500016, India.
Clin Chim Acta. 2010 Nov 11;411(21-22):1817-21. doi: 10.1016/j.cca.2010.08.001. Epub 2010 Aug 10.
Stroke is a complex disease caused by combination of multiple risk factors. Recent findings have suggested that stroke has a strong genetic component. Evidence suggests that variations in the estrogen receptor α (ESR1) gene may influence stroke risk.
The present study was carried out to investigate the role of ESR1 gene polymorphisms [PvuII (rs 2234693) and XbaI (rs 9340799)] with stroke in a South Indian population from Andhra Pradesh. The relationship between ESR1 genotypes with estradiol levels was also investigated in pre- and postmenopausal women.
Four hundred patients with ischemic stroke and three hundred and eighty subjects were enrolled in this case-control study. Ischemic stroke subtypes were classified according to TOAST (Trial of Org 10172 in Acute Stroke Treatment) classification. The ESR1 PvuII and XbaI genotypes were determined by PCR-RFLP method. Serum estradiol was measured by ELISA.
In case of PvuII polymorphism statistically significant difference was observed in the genotypic and allelic frequencies between patients and controls (joint analysis of men and women) (p=0.003 and 0.004 respectively). However, the XbaI genotypes and alleles did not show an association with stroke in the study population. When the analysis was carried out separately for men and women, the PvuII polymorphism did not show significant association with stroke in men; women showed a significant association. Further when women were grouped in to premenopausal and postmenopausal, the premenopausal group did not show a significant association with the polymorphism but significant association with stroke was found in postmenopausal women. A stepwise multiple logistic regression analysis confirmed these findings. Women with pp genotype had low estradiol levels in comparison with PP genotypic individuals (p<0.05). Further evaluating the association of this polymorphism with stroke subtypes, we found significant association of PvuII polymorphism with extracranial atherosclerosis, lacunar and cardioembolic stroke.
In conclusion our results suggest the PvuII gene polymorphism is significantly associated with stroke in postmenopausal women in a South Indian population from Andhra Pradesh. The pp genotypes have average 17β estradiol levels which are significantly low in comparison with PP genotypes. Therefore postmenopausal women with a high frequency of pp genotype are more predisposed to ischemic stroke. However, this is a preliminary study and the results need to be confirmed in a larger cohort.
中风是一种由多种危险因素共同作用引起的复杂疾病。最近的研究结果表明,中风具有很强的遗传成分。有证据表明,雌激素受体 α(ESR1)基因的变异可能会影响中风的风险。
本研究旨在探讨 ESR1 基因多态性[PvuII(rs2234693)和 XbaI(rs9340799)]与印度安得拉邦南部人群中风的关系。还研究了 ESR1 基因型与绝经前和绝经后妇女雌二醇水平的关系。
本病例对照研究纳入了 400 例缺血性中风患者和 380 例对照者。根据 TOAST(急性中风治疗组织 10172 试验)分类,对缺血性中风亚型进行分类。采用 PCR-RFLP 法检测 ESR1 PvuII 和 XbaI 基因型。采用 ELISA 法测定血清雌二醇水平。
在 PvuII 多态性方面,患者和对照组(男女联合分析)的基因型和等位基因频率存在统计学差异(p=0.003 和 0.004)。然而,XbaI 基因型和等位基因与研究人群的中风无关联。当分别对男性和女性进行分析时,PvuII 多态性与男性中风无显著关联;女性则有显著关联。进一步将女性分为绝经前和绝经后,绝经前组与多态性无显著关联,但绝经后女性与中风有显著关联。逐步多元逻辑回归分析证实了这些发现。与 PP 基因型个体相比,pp 基因型女性的雌二醇水平较低(p<0.05)。进一步评估该多态性与中风亚型的关联,我们发现 PvuII 多态性与颅外动脉粥样硬化、腔隙性和心源性栓塞性中风显著相关。
总之,我们的研究结果表明,在印度安得拉邦南部人群中,PvuII 基因多态性与绝经后女性的中风显著相关。与 PP 基因型相比,pp 基因型的平均 17β 雌二醇水平显著降低。因此,具有高频率 pp 基因型的绝经后女性更容易发生缺血性中风。然而,这是一项初步研究,结果需要在更大的队列中得到证实。