代谢功能障碍相关的脂肪变性肝病增加原发性开角型青光眼的风险。

Q2 Medicine
Chao Chen, Jiao Qi, Keke Zhang, Jiaqi Meng, Yi Lu, Fei Wang, Xiangjia Zhu
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引用次数: 0

摘要

目的:肝脏疾病与一系列肝外并发症相关,最近已扩大到包括眼科疾病。然而,其对原发性开角型青光眼(POAG)的影响尚缺乏证据。本研究旨在探讨主要肝脏疾病,包括代谢功能障碍相关脂肪变性肝病(MASLD)、酒精性肝病(ALD)、病毒性肝炎、肝纤维化和肝硬化是否与POAG相关。设计:一项基于英国生物银行队列的前瞻性研究,采用双样本孟德尔随机化(MR)分析来推断因果关系。参与者:在2006年至2010年期间招募了332,345名无青光眼的英国生物银行参与者。方法:研究对象为入院的严重肝病,包括MASLD、ALD、病毒性肝炎、肝纤维化和肝硬化。Cox比例风险模型用于将每种肝病作为时变暴露治疗。mri分析进一步基于MASLD (n = 19,264)和POAG (n = 216,257)的组织学特征队列的全基因组关联研究。主要结局指标:观察分析以风险比(HR)和95%置信区间(CI)估计POAG的风险,MR分析以优势比(OR)和95% CI估计POAG的风险。结果:重度MASLD与POAG风险增加45%相关(HR 1.45;95% ci 1.12-1.87;P = 0.005),而ALD (P = 0.953)、病毒性肝炎(P = 0.519)或肝纤维化和肝硬化(P = 0.794)与POAG的发生没有关联。亚组分析显示,体力活动较多的个体与MASLD相关的POAG风险较高(HR 1.53;95% CI 1.04-2.25, HR 1.39;95% CI 0.99-1.95,交互作用P = 0.033)。MR分析提供的证据表明,MASLD与POAG的高风险存在因果关系(反方差加权模型:OR 1.035;95% ci 1.010-1.061;P = 0.005)。结论:严重的MASLD与POAG发生风险增加纵向相关,MR分析表明存在潜在的因果关系。这些发现提示在MASLD的整体治疗中应考虑POAG检查,并进一步强调肝脏对眼睛健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic dysfunction-associated steatotic liver disease increases the risk of primary open-angle glaucoma.

Purpose: Liver disease is associated with a range of extrahepatic complications, which have recently been expanded to include ophthalmic conditions. However, evidence is lacking regarding its impact on primary open-angle glaucoma (POAG). This study aimed to investigate whether major liver diseases, including metabolic dysfunction-associated steatotic liver disease (MASLD), alcoholic liver disease (ALD), viral hepatitis, and liver fibrosis and cirrhosis, were associated with POAG.

Design: A prospective study based on the UK Biobank cohort with a two-sample Mendelian randomization (MR) analysis for inferring causality.

Participants: A total of 332,345 UK Biobank participants free of glaucoma recruited between 2006 and 2010.

Methods: The exposure of interest was severe liver diseases defined as hospital admission, including MASLD, ALD, viral hepatitis, and liver fibrosis and cirrhosis. Cox proportional hazards models were used with each liver disease treated as a time-varying exposure. The MR analysis was further conducted based on the genome-wide association studies of a histologically characterized cohort for MASLD (n = 19,264) and Internation Glaucoma Genetics Consortium cohort for POAG (n = 216,257).

Main outcome measures: Risk of POAG estimated by hazard ratio (HR) and 95% confidence interval (CI) in observation analysis, and odds ratio (OR) and 95% CI in MR analysis.

Results: Severe MASLD was associated with a 45% increased risk of POAG (HR 1.45; 95% CI 1.12-1.87; P = 0.005), whereas no association was identified between ALD (P = 0.953), viral hepatitis (P = 0.519), or liver fibrosis and cirrhosis (P = 0.794) and incident POAG. Subgroup analysis showed the risk of POAG in relation to MASLD was higher in individuals having more physical activity (HR 1.53; 95% CI 1.04-2.25 vs. HR 1.39; 95% CI 0.99-1.95, P for interaction = 0.033). MR analysis provided evidence that MASLD was causally associated with greater risk of POAG (inverse-variance weighted model: OR 1.035; 95% CI 1.010-1.061; P = 0.005).

Conclusions: Severe MASLD was longitudinally associated with an increased risk of incident POAG, with MR analyses suggesting a potential causal link. These findings suggest POAG examination should be considered in the holistic management of MASLD, and further underscore the impact of the liver on eye health.

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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma Medicine-Medicine (all)
CiteScore
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