甾体激素和促性腺激素途径的遗传变异与多囊卵巢综合征的易感性:系统回顾和荟萃分析。

IF 1.3 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Metabolic syndrome and related disorders Pub Date : 2024-02-01 Epub Date: 2023-10-25 DOI:10.1089/met.2023.0127
Priya Sharma, Abhilash Kumar Singh, Sabyasachi Senapati, Harmanpreet Singh Kapoor, Lajya Devi Goyal, Balpreet Kaur, Pooja Kamra, Preeti Khetarpal
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引用次数: 0

摘要

遗传变异是多囊卵巢综合征(PCOS)的易感因素,这是一种多因素疾病,通常由各种环境因素引发。这项研究调查了参与类固醇生成途径或促性腺激素途径的基因变体与多囊卵巢综合征风险的关系。截至2023年1月11日,在PubMed、Google Scholar、Science Direct和Central Cochrane Library中使用了预定基因的适当关键词进行搜索。普罗旺索(CRD42022275425)。纳入标准:(a)病例对照研究;(b) 基因型或等位基因数据。排除标准为:(a)重复研究;(b) 临床试验、系统综述、荟萃分析或会议摘要、病例报告;(c) 英语以外的语言;(d) 数据不足;e) 最近已经报道了对其进行荟萃分析的遗传变异,但并没有更新的范围。根据数据可用性应用了各种遗传模型。总共选择了7个基因的12个变体进行分析。从47项研究中提取了相关数据,其中包括10584名多囊卵巢综合征受试者和16150名健康对照。荟萃分析表明TOX3 rs4784165[ORs之间存在显著相关性 = 1.08,95%可信区间(1.00-1.16)],HMGA2 rs2272046[ORs = 2.73,95%置信区间(1.97-3.78)],YAP1 rs1894116[或 = 1.22,95%CI(1.13-1.33)]和PCOS风险增加。而FSHR rs2268361[ORs = 0.84,95%CI(0.78-0.89)]与PCOS风险降低相关。当进行敏感性分析时,在加性模型下,CYP19 rs700519和FSHR rs6165的相关性变得显著。此外,随着一项研究的取消,C9Orf3 rs3802457与多囊卵巢综合征风险降低显著相关。CYP19A(rs2470152)、FSHR(rs2349415、rs6166)、C9Orf3(rs4385527)、GnRH1(rs6185)与多囊卵巢综合征风险之间没有显著相关性。我们的研究结果表明,CYP19A(rs700519)、TOX3(rs4784165)、HMGA2(rs2272046)、FSHR(rs6165,rs2268361)、C9orf3(rs3802457)和YAP1(rs1894116)与多囊卵巢综合征的风险相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis.

Genetic variants are predisposing factors to polycystic ovary syndrome (PCOS), a multifactorial condition that often gets triggered due to various environmental factors. The study investigates the association of the variants of genes that are involved in the steroidogenesis pathway or gonadotropin pathway with the risk of PCOS. Appropriate keywords for predetermined genes were used to search in PubMed, Google Scholar, Science Direct, and Central Cochrane Library up to January 11, 2023. PROSPERO (CRD42022275425). Inclusion criteria: (a) case-control study; (b) genotype or allelic data. Exclusion criteria were: (a) duplicate studies; (b) clinical trials, systematic reviews, meta-analysis or conference abstract, case reports; (c) other than the English language; (d) having insufficient data; e) genetic variants for which meta-analysis has been reported recently and does not have a scope of the update. Various genetic models were applied as per data availability. Overall 12 variants of 7 genes were selected for the analysis. Relevant data were extracted from 47 studies which include 10,584 PCOS subjects and 16,150 healthy controls. Meta-analysis indicates a significant association between TOX3 rs4784165 [ORs = 1.08, 95% CI (1.00-1.16)], HMGA2 rs2272046 [ORs = 2.73, 95% CI (1.97-3.78)], YAP1 rs1894116 [OR = 1.22, 95% CI (1.13-1.33)] and increased risk of PCOS. Whereas FSHR rs2268361 [ORs = 0.84, 95% CI (0.78-0.89)] is associated with decreased PCOS risk. When sensitivity analysis was carried out, the association became significant for CYP19 rs700519 and FSHR rs6165 under an additive model. In addition, C9Orf3 rs3802457 became significantly associated with decreased PCOS risk with the removal of one study. Insignificant association was observed for CYP19A (rs2470152), FSHR (rs2349415, rs6166), C9Orf3 (rs4385527), GnRH1 (rs6185) and risk of PCOS. Our findings suggest association of CYP19A (rs700519), TOX3 (rs4784165), HMGA2 (rs2272046), FSHR (rs6165, rs2268361), C9orf3 (rs3802457), and YAP1 (rs1894116) with risk for PCOS.

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来源期刊
Metabolic syndrome and related disorders
Metabolic syndrome and related disorders MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.40
自引率
0.00%
发文量
74
审稿时长
6-12 weeks
期刊介绍: Metabolic Syndrome and Related Disorders is the only peer-reviewed journal focusing solely on the pathophysiology, recognition, and treatment of this major health condition. The Journal meets the imperative for comprehensive research, data, and commentary on metabolic disorder as a suspected precursor to a wide range of diseases, including type 2 diabetes, cardiovascular disease, stroke, cancer, polycystic ovary syndrome, gout, and asthma. Metabolic Syndrome and Related Disorders coverage includes: -Insulin resistance- Central obesity- Glucose intolerance- Dyslipidemia with elevated triglycerides- Low HDL-cholesterol- Microalbuminuria- Predominance of small dense LDL-cholesterol particles- Hypertension- Endothelial dysfunction- Oxidative stress- Inflammation- Related disorders of polycystic ovarian syndrome, fatty liver disease (NASH), and gout
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