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非酒精性脂肪性肝病与冠状动脉疾病:基于血管内皮功能障碍的双向关联。

Non-Alcoholic Fatty Liver Disease and Coronary Artery Disease: A Bidirectional Association Based on Endothelial Dysfunction.

机构信息

First Department of Cardiology, 'Hippokration' General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Endocrine Unit, 2nd Propaedeutic Department of Internal Medicine, School of Medicine, Research Institute and Diabetes Center, Attikon University Hospital, National and Kapodistrian University of Athens, 12641 Athens, Greece.

出版信息

Int J Mol Sci. 2024 Oct 1;25(19):10595. doi: 10.3390/ijms251910595.


DOI:10.3390/ijms251910595
PMID:39408924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11477211/
Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and is regarded as a liver manifestation of metabolic syndrome. It is linked to insulin resistance, obesity, and diabetes mellitus, all of which increase the risk of cardiovascular complications. Endothelial dysfunction (EnD) constitutes the main driver in the progression of atherosclerosis and coronary artery disease (CAD). Several pathophysiological alterations and molecular mechanisms are involved in the development of EnD in patients with NAFLD. Our aim is to examine the association of NAFLD and CAD with the parallel assessment of EnD, discussing the pathophysiological mechanisms and the genetic background that underpin this relationship. This review delves into the management of the condition, exploring potential clinical implications and available medical treatment options to facilitate the deployment of optimal treatment strategies for these patients.

摘要

非酒精性脂肪性肝病(NAFLD)是最常见的慢性肝病病因,被视为代谢综合征的肝脏表现。它与胰岛素抵抗、肥胖和糖尿病有关,所有这些都会增加心血管并发症的风险。内皮功能障碍(EnD)是动脉粥样硬化和冠状动脉疾病(CAD)进展的主要驱动因素。在患有 NAFLD 的患者中,有几种病理生理改变和分子机制涉及 EnD 的发展。我们的目的是检查 NAFLD 和 CAD 与 EnD 的平行评估之间的关联,讨论支持这种关系的病理生理机制和遗传背景。这篇综述深入探讨了该疾病的管理,探讨了潜在的临床意义和可用的治疗方法,以促进为这些患者部署最佳治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ab/11477211/174e3ae8a56d/ijms-25-10595-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ab/11477211/174e3ae8a56d/ijms-25-10595-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ab/11477211/174e3ae8a56d/ijms-25-10595-g001.jpg

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引用本文的文献

[1]
Association of cardiometabolic markers with hepatic steatosis and liver fibrosis in population without obesity and diabetes.

Sci Rep. 2025-5-5

[2]
Metabolic Dysfunction-Associated Steatotic Liver Disease: Pathogenetic Links to Cardiovascular Risk.

Biomolecules. 2025-1-22

[3]
The association between triglyceride-glucose index and neutrophil-lymphocyte ratio and all-cause mortality in the general US population: NHANES 2001-2018.

Front Endocrinol (Lausanne). 2024-12-10

本文引用的文献

[1]
From NAFLD to MASLD: implications of the new nomenclature for preclinical and clinical research.

Nat Metab. 2024-4

[2]
A Phase 3, Randomized, Controlled Trial of Resmetirom in NASH with Liver Fibrosis.

N Engl J Med. 2024-2-8

[3]
Clinical profiles and mortality rates are similar for metabolic dysfunction-associated steatotic liver disease and non-alcoholic fatty liver disease.

J Hepatol. 2024-5

[4]
NIS2+ as a screening tool to optimize patient selection in metabolic dysfunction-associated steatohepatitis clinical trials.

J Hepatol. 2024-2

[5]
The intersection between alcohol-related liver disease and nonalcoholic fatty liver disease.

Nat Rev Gastroenterol Hepatol. 2023-12

[6]
The Economic Burden of Illness.

JAMA Netw Open. 2023-3-1

[7]
NAFLD, MAFLD, and beyond: one or several acronyms for better comprehension and patient care.

Intern Emerg Med. 2023-6

[8]
AASLD Practice Guidance on the clinical assessment and management of nonalcoholic fatty liver disease.

Hepatology. 2023-5-1

[9]
Changes in the global, regional, and national burdens of NAFLD from 1990 to 2019: A systematic analysis of the global burden of disease study 2019.

Front Nutr. 2022-12-21

[10]
Gender Differences in Nonalcoholic Fatty Liver Disease.

Euroasian J Hepatogastroenterol. 2022-7

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