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CGG 重复序列长度与特发性原发性卵巢功能不全严重程度的相关性:荟萃分析。

Association between the CGG repeat lengths and the severity of idiopathic primary ovarian insufficiency: a meta analysis.

机构信息

a Reproductive Medicine Center, Clinical College of People's Liberation Army, Anhui Medical University , Hefei , China.

b Reproductive Medicine Center, the 901th Hospital of the Joint Logistics Support Force of People's Liberation Army , Hefei , China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3116-3122. doi: 10.1080/21691401.2019.1645153.

Abstract

Reports on the association of the CGG repeat length in the gene with the severity of idiopathic POI are inconclusive. Therefore, a meta analysis was performed to investigate the relationship between the expansion of repeat CGG and idiopathic POI risk. Up to January 2019, 18 case-control or cohort studies involving 3394 idiopathic POI patients and 8461 controls were included for meta analysis. Thirteen studies, including 2047 cases and 6912 controls, met our criteria for the assessment of the premutation and intermediate repeat length in patients with overt POI. Compared with controls, gene premutation is significantly associated with overt POI (OR = 8.13; 95% CI: 4.35-15.19;  < .00001), whereas there was no significant correlation between intermediate repeat length and overt POI (OR = 0.86; 95% CI: 0.62-1.18;  = .34). Seven studies, representing 1347 patients and 1948 controls, were eligible for evaluation of the premutation and intermediate repeat length in occult POI. The association between premutation and occult POI was significant ( < .00001), with a pooled fixed effects OR of 11.32 (4.45-28.80), and no significant correlation of intermediate size to occult POI was found in the case-control comparison (OR = 1.00; 95% CI: 0.68-1.47;  = .98). There is a close association between premutation of the gene and increased susceptibility to idiopathic POI of each stage and no correlation between intermediate repeat length of the gene and the severity of idiopathic POI.

摘要

关于基因 CGG 重复长度与特发性 POI 严重程度的相关性的报告尚无定论。因此,进行了一项荟萃分析,以研究重复 CGG 扩展与特发性 POI 风险之间的关系。截至 2019 年 1 月,共纳入了 18 项病例对照或队列研究,涉及 3394 例特发性 POI 患者和 8461 例对照,进行荟萃分析。有 13 项研究(包括 2047 例病例和 6912 例对照)符合我们评估显性 POI 患者的前突变和中间重复长度的标准。与对照组相比,基因前突变与显性 POI 显著相关(OR=8.13;95%CI:4.35-15.19; < .00001),而中间重复长度与显性 POI 无显著相关性(OR=0.86;95%CI:0.62-1.18; = .34)。有 7 项研究(代表 1347 例患者和 1948 例对照)符合评估隐匿性 POI 中前突变和中间重复长度的标准。前突变与隐匿性 POI 之间存在显著相关性( < .00001),合并固定效应 OR 为 11.32(4.45-28.80),病例对照比较中未发现中间大小与隐匿性 POI 有显著相关性(OR=1.00;95%CI:0.68-1.47; = .98)。基因前突变与各阶段特发性 POI 的易感性增加密切相关,而基因中间重复长度与特发性 POI 的严重程度无关。

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