Gene polymorphism of leptin and risk for heart disease, obesity, and high BMI: a systematic review and pooled analysis in adult obese subjects.

IF 1.1 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Hormone Molecular Biology and Clinical Investigation Pub Date : 2023-03-01 DOI:10.1515/hmbci-2022-0020
Fatemeh Khaki-Khatibi, Behrouz Shademan, Reza Gholikhani-Darbroud, Alireza Nourazarian, Saeed Radagdam, Maghsoud Porzour
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引用次数: 2

Abstract

Objectives: Leptin polymorphism (LEP) has been associated with coronary heart disease (CAD), obesity, and high body mass index (BMI). However, we performed a systematic review and meta-analysis to discover the association because previous studies reached different conclusions.

Methods: Review Manager, version 5.3.5, and Stata, version 15.0, were used for statistical analysis. We calculated the effect size of the studies using the OR with the corresponding 95% CI, and two-sided (bilateral) p-values of 0.05 were considered significant. To determine heterogeneity among the selected studies, the Q test and I2 statistics were used. Meta-regression was used to examine the disease (heart disease, obesity, and high BMI) and heterogeneity between these subgroups.

Results: Eleven studies with 18,984 subjects were included in this study. The G-2548A (rs12112075), rs7799039, and A19G (rs2167270) polymorphisms of the leptin gene (but not the Lys656Asn (rs1805094) polymorphism) are associated with an increased risk of cardiovascular disease. Our pooled analysis revealed an association between the G-2548A (rs12112075) polymorphism and heart disease, high BMI, and obesity. This indicates that individuals carrying the AA allele are at an increased risk for heart disease, high BMI, and obesity. People with heart failure and coronary artery disease did not have the rs7799039 polymorphism or its alleles linked to them.

Conclusions: Combined analysis of data from current and published research suggests that the leptin gene polymorphisms G-2548A (rs12112075), rs7799039, and A19G (rs2167270) (but not the Lys656Asn (rs1805094) polymorphism) are associated with an increased risk of cardiovascular disease. Further research is needed to understand this association.

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瘦素基因多态性与心脏病、肥胖和高BMI风险:成人肥胖受试者的系统回顾和汇总分析
目的:瘦素多态性(LEP)与冠心病(CAD)、肥胖和高体重指数(BMI)相关。然而,由于之前的研究得出了不同的结论,我们进行了系统回顾和荟萃分析来发现这种关联。方法:采用Review Manager软件5.3.5版本,Stata软件15.0版本进行统计分析。我们使用OR和相应的95% CI计算研究的效应大小,双侧(双侧)p值0.05被认为是显著的。为了确定所选研究之间的异质性,使用Q检验和I2统计。meta回归用于检查疾病(心脏病、肥胖和高BMI)和这些亚组之间的异质性。结果:本研究共纳入11项研究,共18,984名受试者。瘦素基因的G-2548A (rs12112075)、rs7799039和A19G (rs2167270)多态性(而不是Lys656Asn (rs1805094)多态性)与心血管疾病风险增加相关。我们的汇总分析显示G-2548A (rs12112075)多态性与心脏病、高BMI和肥胖之间存在关联。这表明携带AA等位基因的人患心脏病、高BMI和肥胖的风险更高。患有心力衰竭和冠状动脉疾病的人没有rs7799039多态性或与其相关的等位基因。结论:当前和已发表研究数据的综合分析表明,瘦素基因多态性G-2548A (rs12112075)、rs7799039和A19G (rs2167270)(而不是Lys656Asn (rs1805094)多态性)与心血管疾病风险增加相关。需要进一步的研究来理解这种联系。
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Hormone Molecular Biology and Clinical Investigation
Hormone Molecular Biology and Clinical Investigation BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
2.60
自引率
0.00%
发文量
55
期刊介绍: Hormone Molecular Biology and Clinical Investigation (HMBCI) is dedicated to the provision of basic data on molecular aspects of hormones in physiology and pathophysiology. The journal covers the treatment of major diseases, such as endocrine cancers (breast, prostate, endometrium, ovary), renal and lymphoid carcinoma, hypertension, cardiovascular systems, osteoporosis, hormone deficiency in menopause and andropause, obesity, diabetes, brain and related diseases, metabolic syndrome, sexual dysfunction, fetal and pregnancy diseases, as well as the treatment of dysfunctions and deficiencies. HMBCI covers new data on the different steps and factors involved in the mechanism of hormone action. It will equally examine the relation of hormones with the immune system and its environment, as well as new developments in hormone measurements. HMBCI is a blind peer reviewed journal and publishes in English: Original articles, Reviews, Mini Reviews, Short Communications, Case Reports, Letters to the Editor and Opinion papers. Ahead-of-print publishing ensures faster processing of fully proof-read, DOI-citable articles.
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