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土耳其人群中载脂蛋白C-III基因多态性(rs2854116和rs2854117)与代谢功能障碍相关脂肪性肝病(MASLD)易感性的关联

Association of Apolipoprotein C-III Gene Polymorphisms (rs2854116 and rs2854117) with Susceptibility to Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) in a Turkish Population.

作者信息

Karaagac Damla, Morkuzu Suat, Senkal Naci, Bilgin Ersel, Oyacı Yasemin, Tükek Tufan, Pehlivan Sacide, Medetalibeyoglu Alpay

机构信息

Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, 34452 İstanbul, Turkey.

Department of Family Medicine, Istanbul Medical Faculty, Istanbul University, 34452 İstanbul, Turkey.

出版信息

Medicina (Kaunas). 2025 Aug 18;61(8):1479. doi: 10.3390/medicina61081479.

Abstract

: Metabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by the accumulation of fat in the liver, progressing from simple steatosis to various complications, with increasing prevalence in the modern world. Our study aimed to investigate the relationship between MASLD pathogenesis and the presence of apolipoprotein C-III (ApoC-III) gene variants rs2854116 and rs2854117 by comparing allele and genotype frequencies between MASLD patients and healthy individuals, as well as analyzing their association with biochemical parameters in Turkish populations. : The study included 202 MASLD patients and 100 healthy controls who presented to our outpatient clinic. MASLD presence was determined by ultrasonography (USG). The demographic, laboratory, and clinical data of the participants were recorded. ApoC-III gene variants rs2854116 and rs2854117 were genotyped using the Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) method from genomic DNA samples obtained from blood. : The genotype and allele frequencies of ApoC-III gene variants rs2854116 and rs2854117 did not show significant differences between patient and healthy groups ( > 0.05). When biochemical parameters were evaluated, the LDH value of rs2854116 variant CT/CC genotype carriers was found to be significantly higher than TT genotype carriers ( = 0.016). : We observed a high prevalence of MASLD in our Turkish cohort. However, the specific genetic variants we investigated were not associated with MASLD status. This suggests that these variants may not be significant contributing factors to MASLD in this population.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)的特征是肝脏中脂肪堆积,从单纯性脂肪变性发展到各种并发症,在现代社会中的患病率不断上升。我们的研究旨在通过比较MASLD患者和健康个体之间的等位基因和基因型频率,以及分析它们与土耳其人群生化参数的关联,来探讨MASLD发病机制与载脂蛋白C-III(ApoC-III)基因变体rs2854116和rs2854117之间的关系。

该研究纳入了到我们门诊就诊的202例MASLD患者和100名健康对照。通过超声检查(USG)确定是否存在MASLD。记录参与者的人口统计学、实验室和临床数据。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对从血液中获得的基因组DNA样本进行ApoC-III基因变体rs2854116和rs2854117的基因分型。

ApoC-III基因变体rs2854116和rs2854117的基因型和等位基因频率在患者组和健康组之间没有显著差异(>0.05)。在评估生化参数时,发现rs2854116变体CT/CC基因型携带者的乳酸脱氢酶(LDH)值显著高于TT基因型携带者(=0.016)。

我们在土耳其队列中观察到MASLD的高患病率。然而,我们研究的特定基因变体与MASLD状态无关。这表明这些变体可能不是该人群中MASLD的重要促成因素。

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