Association of four insulin resistance indices with liver‐related adverse outcomes: A prospective cohort study

医学 前瞻性队列研究 胰岛素抵抗 内科学 不利影响 队列研究 疾病 队列 判别式 联想(心理学) 病例对照研究 糖尿病 风险评估 梅德林 胰岛素
作者
Xiao‐Meng Wang,Hao Yu Yan,Wen‐Fang Zhong,Jia‐Hao Xie,Huan Chen,Junjie Wang,Wei‐qi Song,Dong Shen,P. Zhang,Xi Zhang,Jiao‐Jiao Ren,Dan Liu,Zhi‐Hao Li,Chen Mao
出处
期刊:Diabetes, Obesity and Metabolism [Wiley]
卷期号:28 (5): 3598-3611 被引量:8
标识
DOI:10.1111/dom.70536
摘要

AIMS: Longitudinal evidence is limited on how changes in insulin resistance (IR) indices-including estimated glucose disposal rate (eGDR), triglyceride-glucose index (TyG), metabolic score for insulin resistance (METS-IR), and lipid accumulation product (LAP)-relate to liver-related adverse outcomes. This study aims to assess their associations and the discriminative performance of IR indices. MATERIALS AND METHODS: IR indices were calculated from UK Biobank data at two surveys (2006-2010 and 2012-2013). Liver-related adverse outcomes, including liver disease, major adverse liver outcomes (MALO), and metabolic dysfunction-associated steatotic liver disease (MASLD), were identified via ICD-10 codes. K-means clustering defined four change patterns per index, and cumulative averages reflected long-term exposure. Cox regression estimated hazard ratios (HRs) and 95% confidence intervals (CIs). Discriminative performance was assessed using receiver operating characteristic (ROC) curves. RESULTS: The participants were followed for a mean of 9.7 years. Compared with persistently low eGDR levels, the persistently high group was associated with significantly lower risks of liver-related adverse outcomes, with HRs of 0.52 (95% Cl: 0.35-0.77) for liver disease, 0.30 (0.19-0.49) for MALO, and 0.31 (0.17-0.55) for MASLD. In contrast, persistently high TyG, METS-IR, and LAP were associated with increased risks of liver-related adverse outcomes, with METS-IR showing the strongest association with MASLD (HR = 10.50, 4.00-27.58). Cumulative eGDR was inversely associated with liver-related adverse outcomes (per 1 SD increase: HRs ranged from 0.52 to 0.68), whereas TyG, METS-IR, and LAP were positively associated, with METS-IR showing the strongest link to MASLD (HR = 1.70, 1.48-1.96). LAP demonstrated the highest discriminative performance in ROC analysis, particularly in females and those under 60 (AUC for MALO in females: up to 0.813). CONCLUSIONS: Dynamic changes in IR indices are independently associated with liver-related adverse outcomes. Among these indices, LAP showed relatively stronger discriminative performance in females. Collectively, these indices may have potential utility as non-invasive markers for liver disease risk stratification.
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