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中国南方代谢综合征与 ACE2 基因遗传变异的病例对照研究。

Genetic variations in ACE2 gene associated with metabolic syndrome in southern China: a case-control study.

机构信息

Department of Geriatrics, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, Fujian, People's Republic of China.

Department of Geriatrics, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, Fujian, People's Republic of China.

出版信息

Sci Rep. 2024 May 7;14(1):10505. doi: 10.1038/s41598-024-61254-5.

Abstract

Metabolic syndrome (MetS) is closely related to cardiovascular and cerebrovascular diseases, and genetic predisposition is one of the main triggers for its development. To identify the susceptibility genes for MetS, we investigated the relationship between angiotensin-converting enzyme 2 (ACE2) single nucleotide polymorphisms (SNPs) and MetS in southern China. In total, 339 MetS patients and 398 non-MetS hospitalized patients were recruited. Four ACE2 polymorphisms (rs2074192, rs2106809, rs879922, and rs4646155) were genotyped using the polymerase chain reaction-ligase detection method and tested for their potential association with MetS and its related components. ACE2 rs2074192 and rs2106809 minor alleles conferred 2.485-fold and 3.313-fold greater risks of MetS in women. ACE2 rs2074192 and rs2106809 variants were risk factors for obesity, diabetes, and low-high-density lipoprotein cholesterolemia. However, in men, the ACE2 rs2074192 minor allele was associated with an approximately 0.525-fold reduction in MetS prevalence. Further comparing the components of MetS, ACE2 rs2074192 and rs2106809 variants reduced the risk of obesity and high triglyceride levels. In conclusion, ACE2 rs2074192 and rs2106809 SNPs were independently associated with MetS in a southern Chinese population and showed gender heterogeneity, which can be partially explained by obesity. Thus, these SNPs may be utilized as predictive biomarkers and molecular targets for MetS. A limitation of this study is that environmental and lifestyle differences, as well as genetic heterogeneity among different populations, were not considered in the analysis.

摘要

代谢综合征(MetS)与心脑血管疾病密切相关,遗传易感性是其发展的主要触发因素之一。为了确定 MetS 的易感基因,我们研究了血管紧张素转换酶 2(ACE2)单核苷酸多态性(SNP)与中国南方 MetS 的关系。共纳入 339 例 MetS 患者和 398 例非 MetS 住院患者。采用聚合酶链反应-连接酶检测法检测 ACE2 四个多态性(rs2074192、rs2106809、rs879922 和 rs4646155),并检测其与 MetS 及其相关成分的潜在关联。ACE2 rs2074192 和 rs2106809 小等位基因使女性患 MetS 的风险分别增加了 2.485 倍和 3.313 倍。ACE2 rs2074192 和 rs2106809 变体是肥胖、糖尿病和低-高密度脂蛋白胆固醇血症的危险因素。然而,在男性中,ACE2 rs2074192 小等位基因与 MetS 患病率降低约 0.525 倍相关。进一步比较 MetS 的组成部分,ACE2 rs2074192 和 rs2106809 变体降低了肥胖和高甘油三酯水平的风险。总之,ACE2 rs2074192 和 rs2106809 SNP 在中国南方人群中与 MetS 独立相关,且具有性别异质性,这可以部分用肥胖来解释。因此,这些 SNP 可作为 MetS 的预测生物标志物和分子靶点。本研究的局限性在于在分析中未考虑环境和生活方式差异以及不同人群的遗传异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7c/11076479/27de49a4882e/41598_2024_61254_Fig1_HTML.jpg

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