长期随访人群中胰岛素与肝功能检查、肝病和肝硬化之间的关系

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Andreas Schult, Kirsten Mehlig, Kurt Svärdsudd, Sven Wallerstedt, Cecilia Björkelund, Per-Olof Hansson, Henrik Zetterberg, Jerzy Kaczynski
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引用次数: 0

摘要

背景:胰岛素抵抗是一种以胰岛素水平升高为特征的心脏代谢危险因素。在横断面研究中,它与脂肪肝疾病和肝功能测试(LFT)升高有关,但来自队列研究的数据很少。目的:在一项基于人群的回顾性队列研究中,探讨胰岛素与病理性LFT、肝脏疾病和肝硬化之间的关系。方法:使用来自前瞻性队列研究的857名男性和1228名女性的人体测量学和心脏代谢因素。在基线后8年至24年的两个时间点获得LFT。肝脏疾病诊断来自全国登记。分析了胰岛素水平与LFT升高或肝病和肝硬化之间的关系。结果:女性随访总人数为54054人年,男性为27556人年。在随访期间,胰岛素水平与LFT升高呈正相关,而体力活动与咖啡摄入量呈负相关。胰岛素水平较高且饮酒量高于MASLD阈值的个体患两种肝脏疾病的风险均增加,调整后的危险比(aHR)为4.3 (95%CI: 1.6-14.6),肝硬化(aHR = 4.8, 95%CI: 1.6-14.6)。结论:这项以人群为基础的研究提供了证据,表明高胰岛素水平是肝酶升高和临床表现为肝脏疾病的危险因素。结果支持代谢功能障碍与肝脏疾病相关的概念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between insulin and liver function tests, liver disease and cirrhosis in population-based cohorts with long term follow-up.

Background: Insulin resistance is a cardiometabolic risk factor characterized by elevated insulin levels. It is associated with fatty liver disease and elevated liver function tests (LFT) in cross-sectional studies, but data from cohort studies are scarce.

Aim: To investigate the association between insulin and pathological LFT, liver disease, and cirrhosis in a population-based retrospective cohort study.

Methods: Anthropometric and cardiometabolic factors of 857 men and 1228 women from prospective cohort studies were used. LFT were obtained at two time points 8 years to 24 years after baseline. Liver disease diagnoses were obtained from nationwide registries. The association between insulin levels and the development of elevated LFT or liver disease and cirrhosis was analyzed.

Results: Total follow-up was 54054 person-years for women and 27556 person-years for men. Insulin levels were positively correlated with elevated LFT during follow-up, whereas physical activity and coffee consumption were negatively correlated. Individuals with both insulin levels in the upper tertile and alcohol consumption above MASLD thresholds had an increased risk for both liver disease, adjusted hazard ratio (aHR) of 4.3 (95%CI: 1.6-14.6) and cirrhosis (aHR = 4.8, 95%CI: 1.6-14.6).

Conclusion: This population-based study provides evidence that high insulin levels are a risk factor for development of elevated liver enzymes and clinically manifest liver disease. The results support the concept of metabolic dysfunction associated liver disease.

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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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