Association of Calpain10 polymorphisms with polycystic ovarian syndrome susceptibility: a systematic review and meta-analysis with trial sequential analysis

被引:1
作者
Li, Yamei [1 ,2 ]
Han, Ting [2 ]
Wang, Yingxia [2 ]
Gao, Jie [2 ]
Zhang, Jianglin [2 ]
Wu, Yinglan [2 ]
Luo, Jiayou [3 ]
机构
[1] Hunan Prov Maternal & Child Hlth Care Hosp, NHC Key Lab Birth Defect Res & Prevent, Changsha, Peoples R China
[2] Hunan Prov Maternal & Child Hlth Care Hosp, Dept Women Hlth Care, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Sch Publ Hlth, Dept Maternal & Child Hlth, Changsha, Peoples R China
关键词
Calpain10; gene; polymorphism; polycystic ovarian syndrome; systematic review; meta-analysis; false-positive report probability; trial sequential analysis; TYPE-2; DIABETES-MELLITUS; INSULIN-RESISTANCE; GENETIC POLYMORPHISMS; CAPN10; UCSNP-43; SYNDROME PCOS; WOMEN; RISK; MECHANISMS; SECRETION; ANDROGENS;
D O I
10.3389/fgene.2023.1153960
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Insulin resistance plays an important role in the pathogenesis of polycystic ovarian syndrome (PCOS). Calpain10 (CAPN10) gene was the first identified susceptibility gene for type 2 diabetes mellitus and closely related to insulin sensitivity. A lot of research attention has been attracted on the relationship between CAPN10 polymorphisms and PCOS risk, but they didn't reach a consistent conclusion. We therefore performed this systematic review and meta-analysis to assess the association of CAPN10 common variants with PCOS susceptibility. A total of 21 studies were eligible for inclusion. Meta-analyses were done for 5 variants that had at least two data sources: UCSNP-19, -43, -44, -56 and -63. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated under five genetic models. Subgroup analyses by ethnicity, PCOS diagnostic criteria, and source of controls were conducted. Moreover, false-positive report probability (FPRP) test and trial sequential analysis (TSA) were performed to assess the significant associations. The results showed a possible negative association between UCSNP-19 and PCOS risk (ins/ins vs. del/del + del/ins: OR = 0.84, 95% CI: 0.72-0.98). In subgroup analyses, FPRP test indicated that noteworthy associations were observed in mixed ethnicities for UCSNP-43 (A vs. G: OR = 1.81, 95% CI: 1.17-2.79; AA + AG vs. GG: OR = 2.14, 95% CI: 1.20-3.80) and in Asians for UCSNP-44 (CC vs. TT: OR = 2.07, 95% CI: 1.21-3.51; CC vs. CT + TT: OR = 2.19, 95% CI: 1.31-3.69), but TSA plots showed that the accumulated sample sizes of these associations were insufficient to draw firm conclusions. In summary, our study suggested that UCSNP-19, UCSNP-43, and UCSNP-44 in CAPN10 gene may be involved in PCOS susceptibility. These findings warrant further studies.
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页数:14
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