APOC3和ANGPTL8基因多态性与MASLD风险的关系及甘油三酯对中国人群MASLD的中介作用

IF 5.3
Jia Pan, Xue Wang, Youjin Zhang, Ting Wang, Saiqun Lv, Xiaoli Zhang, Yuanyuan Zhou, Tao Peng, Yongyan Song
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引用次数: 0

摘要

载脂蛋白C3(APOC3)和血管生成素样蛋白8(ANGPTL8)基因与脂质代谢有关。APOC3 和 ANGPTL8 基因中的单核苷酸多态性(SNPs)与代谢功能障碍相关性脂肪性肝病(MASLD)之间的关系仍存在争议。本研究旨在调查 APOC3 和 ANGPTL8 基因中特定 SNPs 与 MASLD 风险之间的关联,尤其关注甘油三酯 (TG) 的中介作用。该研究共招募了 440 名参与者,并将其分为 MASLD 组和对照组。采用聚合酶链式反应-限制性片段长度多态性或桑格测序方法对 APOC3 SNP(rs5128、rs2854116 和 rs2854117)和 ANGPTL8 SNP(rs2278426)进行了基因分型。采用多变量逻辑回归估计了这些 SNP 与 MASLD 风险之间的关联,并进行了中介分析以评估 TG 的潜在中介效应。我们发现,APOC3 SNP与MASLD风险相关,几率比(ORs)增加表明MASLD风险更高:rs5128 CG + GG基因型(OR = 1.8,95% CI = 1.1-2.8)、rs2854116 TC + CC基因型(OR = 1.9,95% CI = 1.1-3.1)和rs2854117 CT + TT基因型(OR = 1.9,95% CI = 1.2-3.2)。ANGPTL8 rs2278426 与 MASLD 之间没有关联(p > 0.05)。中介分析显示,TG 对这些关系有明显的中介作用,rs5128 的中介作用占 80.25%,rs2854116 的中介作用占 64.61%,rs2854117 的中介作用占 62.59%。总之,APOC3 的多态性(rs5128、rs2854116 和 rs2854117)与 MASLD 风险相关,而 TG 是潜在的中介因素。相比之下,ANGPTL8 rs2278426多态性与MASLD没有任何关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Associations Between APOC3 and ANGPTL8 Gene Polymorphisms With MASLD Risk and the Mediation Effect of Triglyceride on MASLD in the Chinese Population

Associations Between APOC3 and ANGPTL8 Gene Polymorphisms With MASLD Risk and the Mediation Effect of Triglyceride on MASLD in the Chinese Population

Apolipoprotein C3 (APOC3) and angiopoietin-like protein 8 (ANGPTL8) genes are related to lipid metabolism. The relationships between single nucleotide polymorphisms (SNPs) in the APOC3 and ANGPTL8 genes with metabolic dysfunction-associated steatotic liver disease (MASLD) remain controversial. This study aimed to investigate the associations between specific SNPs in the APOC3 and ANGPTL8 genes and MASLD risk, with a particular focus on the mediating role of triglycerides (TG). A total of 440 participants were enrolled and categorised into MASLD and control groups. Genotyping of APOC3 SNPs (rs5128, rs2854116 and rs2854117) and ANGPTL8 SNP (rs2278426) was conducted using polymerase chain reaction–restriction fragment length polymorphism or Sanger sequencing methods. Multivariate logistic regression was employed to estimate the associations between these SNPs and MASLD risk, and mediation analysis was performed to assess the potential mediating effect of TG. We found that APOC3 SNPs were associated with MASLD risk, with increased odds ratios (ORs) indicating a higher risk of MASLD: rs5128 CG + GG genotype (OR = 1.8, 95% CI = 1.1–2.8), rs2854116 TC + CC genotype (OR = 1.9, 95% CI = 1.1–3.1) and rs2854117 CT + TT genotype (OR = 1.9, 95% CI = 1.2–3.2). No association was found between ANGPTL8 rs2278426 and MASLD (p > 0.05). Mediation analysis revealed that TG significantly mediated these relationships, accounting for 80.25% of the effect for rs5128, 64.61% for rs2854116 and 62.59% for rs2854117. In summary, polymorphisms in APOC3 (rs5128, rs2854116 and rs2854117) were associated with MASLD risk, with TG serving as a potential mediating factor. In contrast, ANGPTL8 rs2278426 polymorphism did not show any association with MASLD.

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11.50
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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