PvuII and XbaI in Estrogen Receptor 1 (ESR1) Polymorphisms and Susceptibility to Endometriosis Risk

雌激素受体α 子宫内膜异位症 雌激素受体 雌激素 内科学 医学 雌激素受体 内分泌学 乳腺癌 癌症
作者
Jingwen Wang,Rong Hu,Jingjing Wang,Qian He
出处
期刊:Clinical Laboratory [Clinical Laboratory Publications]
卷期号:66 (08/2020) 被引量:2
标识
DOI:10.7754/clin.lab.2020.191209
摘要

Studies have shown that variants in PvuII and XbaI loci are associated with the occurrence and progression of endometriosis (EM), while the results were in great debate.A systematic review and meta-analysis were conducted to evaluate the role of PvuII and XbaI polymor-phisms in estrogen receptors (ESR1). The primary sources of the reviewed studies through December 2018, with restriction on the language of English and Chinese, were Pubmed and Embase and CNKI. The pooled odds ratio 95% confidence intervals (CIs) were calculated to evaluate the associations of Pvull and Xbal polymorphisms with the risk of EM by using the STATA 14.0 software.A total of 18 studies with 4,975 patients, 2,222 in the case group, 2,753 in the control group, were in the final analysis. Overall pooled outcomes did not indicate significant correlations between the ESR1 Pvull/Xbal polymorphisms and the EM development. In subgroup analysis, PvuII was associated with endometriosis only for stage I - III and only under a recessive model (OR = 1.61, 95% CI: 1.03 to 2.07; p = 0.03). Xbal was associated with endometriosis only for the non-PCR-RFLP genotype method and also only under a recessive model (OR = 2.10, 95% CI: 1.21 to 4.47; p = 0.04).This present meta-analysis reported that polymorphisms of PvuII or Xbal were not related to the susceptibility to EM except for a slight association of stage I-III endometriosis and non-PCR-RFLP under recessive model. Future, well-designed large studies are eagerly awaited to confirm our conclusions.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
uu完成签到,获得积分10
刚刚
刚刚
小清新发布了新的文献求助10
刚刚
刚刚
小马甲应助OK采纳,获得10
1秒前
科研通AI6.3应助胡123456789采纳,获得10
1秒前
Jason+Fang发布了新的文献求助10
2秒前
852应助背后的傥采纳,获得30
2秒前
黄寒梅发布了新的文献求助10
2秒前
完美世界应助huogo采纳,获得10
3秒前
纪年完成签到,获得积分10
3秒前
肉肉发布了新的文献求助10
3秒前
3秒前
柠檬水要加冰完成签到,获得积分10
3秒前
九歌完成签到,获得积分10
4秒前
虚幻远侵完成签到,获得积分10
4秒前
5秒前
5秒前
5秒前
xuge发布了新的文献求助10
6秒前
努力发布了新的文献求助10
6秒前
薛小飞完成签到 ,获得积分10
6秒前
7秒前
7秒前
lsl应助黄寒梅采纳,获得10
8秒前
阳佟亦旋完成签到,获得积分10
8秒前
9秒前
ZzRG发布了新的文献求助10
9秒前
哆啦完成签到,获得积分10
10秒前
10秒前
10秒前
人生几何发布了新的文献求助10
10秒前
跨材料发布了新的文献求助10
11秒前
11秒前
11秒前
李健的粉丝团团长应助yyy采纳,获得10
12秒前
12秒前
糕糕完成签到,获得积分10
12秒前
13秒前
13秒前
高分求助中
Ideology and Meaning-Making under the Putin Regime 750
Introduction to Industrial/Organizational Psychology 600
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
Isomerism In Coordination Compounds 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6934894
求助须知:如何正确求助?哪些是违规求助? 8621845
关于积分的说明 18287196
捐赠科研通 6361973
什么是DOI,文献DOI怎么找? 3075048
关于科研通互助平台的介绍 2112432
邀请新用户注册赠送积分活动 2052528