Mozafari Sima, Ashoori Marziyeh, Emami Meybodi Seyed Mahdi, Solhi Roya, Mirjalili Seyed Reza, Firoozabadi Ali Dehghani, Soltani Sepideh
Yazd Cardiovascular Research Center, Non-Communicable Diseases Research Institute, Shahid Sadoughi University of Medical Sciences, Afshar Hospital, Jomhouri Blvd., Yazd, 8917945556, Iran.
Rasool Akram Medical Complex, Clinical Research Development Center, Tehran, Iran.
BMC Genomics. 2024 Jun 12;25(1):590. doi: 10.1186/s12864-024-10493-x.
The association between Apolipoprotein A5 (APOA5) genetic polymorphisms and susceptibility to metabolic syndrome (MetS) has been established by many studies, but there have been conflicting results from the literature. We performed a meta-analysis of observational studies to evaluate the association between APOA5 gene polymorphisms and the prevalence of MetS.
PubMed, Web of Science, Embase, and Scopus were searched up to April 2024. The random effects model was used to estimate the odds ratios (ORs) and 95% confidence intervals (CI) of the association between APOA5 gene polymorphisms and the prevalence of MetS development. The potential sources of heterogeneity were evaluated by subgroup analyses and sensitivity analyses.
A total of 30 studies with 54,986 subjects (25,341 MetS cases and 29,645 healthy controls) were included. The presence of rs662799 and rs651821 polymorphisms is associated with an approximately 1.5-fold higher likelihood of MetS prevalence (OR = 1.42, 95% CI: 1.32, 1.53, p < 0.001; I = 67.1%; P-heterogeneity < 0.001; and OR = 1.50, 95% CI: 1.36-1.65, p < 0.001), respectively. MetS is also more prevalent in individuals with the genetic variants rs3135506 and rs2075291. There was no evidence of a connection with rs126317.
The present findings suggest that polymorphisms located in the promoter and coding regions of the APOA5 gene are associated with an increased prevalence of MetS in the adult population. Identifying individuals with these genetic variations could lead to early disease detection and the implementation of preventive strategies to reduce the risk of MetS and its related health issues. However, because the sample size was small and there was evidence of significant heterogeneity for some APOA5 gene polymorphisms, these results need to be confirmed by more large-scale and well-designed studies.
多项研究已证实载脂蛋白A5(APOA5)基因多态性与代谢综合征(MetS)易感性之间存在关联,但文献报道的结果相互矛盾。我们进行了一项观察性研究的荟萃分析,以评估APOA5基因多态性与MetS患病率之间的关联。
检索截至2024年4月的PubMed、Web of Science、Embase和Scopus数据库。采用随机效应模型估计APOA5基因多态性与MetS发生患病率之间关联的比值比(OR)和95%置信区间(CI)。通过亚组分析和敏感性分析评估异质性的潜在来源。
共纳入30项研究,涉及54,986名受试者(25,341例MetS患者和29,645名健康对照)。rs662799和rs651821多态性的存在分别与MetS患病率高出约1.5倍相关(OR = 1.42,95% CI:1.32,1.53,p < 0.001;I² = 67.1%;P异质性 < 0.001;以及OR = 1.50,95% CI:1.36 - 1.65,p < 0.001)。MetS在具有rs3135506和rs2075291基因变异的个体中也更为普遍。没有证据表明与rs126317存在关联。
目前的研究结果表明,APOA5基因启动子和编码区的多态性与成年人群中MetS患病率增加有关。识别具有这些基因变异的个体可能有助于早期疾病检测,并实施预防策略以降低MetS及其相关健康问题的风险。然而,由于样本量较小且某些APOA5基因多态性存在显著异质性的证据,这些结果需要更多大规模、设计良好的研究来证实。