{"title":"肝硬化的心脏代谢风险因素和临床过程","authors":"","doi":"10.1016/j.dld.2024.08.018","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>The global prevalence of Metabolic Dysfunction-Associated Liver Disease (MASLD) is dramatically increasing with the diffusion of cardiometabolic risk factors. The aim of the present study was to assess the natural course of liver cirrhosis, in terms of decompensation, development of hepatocellular carcinoma and mortality, in relation to the presence of cardiometabolic risk factors (type 2 diabetes mellitus, obesity, arterial hypertension, low HDL levels, hypertriglyceridemia). Patients: 667 patients with liver cirrhosis (50 with MASLD aetiology, 167 with non-MASLD aetiology, and 450 with a non-MASLD etiological factor plus the presence of at least one cardiometabolic risk factor) followed at the University and General Hospital of Padua, Italy, from 1998 to 2022, were included.</p></div><div><h3>Results</h3><p>No difference in the occurrence of cirrhosis decompensating events and development of hepatocellular carcinoma was observed, whereas patients in the MASLD or mixed group had 4-3-fold higher all-cause mortality and significantly lower 3-years survival compared to patients with non-MASLD cirrhosis, despite a better liver function at enrolment. Hypertriglyceridemia and low HDL levels were the less prevalent cardiometabolic factors, but those associated with the highest risk of cirrhosis decompensation. Hypertriglyceridemia was also associated with an increased risk of mortality. Arterial hypertension was associated with a reduced risk of cirrhosis decompensation, but a higher risk of mortality.</p></div><div><h3>Conclusion</h3><p>Compared to patients with non-MASLD cirrhosis, those with cardiometabolic risk factors had similar rates of liver cirrhosis decompensation but higher overall mortality. Hypertriglyceridemia was associated with a high risk of both liver decompensation and death.</p></div>","PeriodicalId":11268,"journal":{"name":"Digestive and Liver Disease","volume":null,"pages":null},"PeriodicalIF":4.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiometabolic risk factors and clinical course of liver cirrhosis\",\"authors\":\"\",\"doi\":\"10.1016/j.dld.2024.08.018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>The global prevalence of Metabolic Dysfunction-Associated Liver Disease (MASLD) is dramatically increasing with the diffusion of cardiometabolic risk factors. The aim of the present study was to assess the natural course of liver cirrhosis, in terms of decompensation, development of hepatocellular carcinoma and mortality, in relation to the presence of cardiometabolic risk factors (type 2 diabetes mellitus, obesity, arterial hypertension, low HDL levels, hypertriglyceridemia). Patients: 667 patients with liver cirrhosis (50 with MASLD aetiology, 167 with non-MASLD aetiology, and 450 with a non-MASLD etiological factor plus the presence of at least one cardiometabolic risk factor) followed at the University and General Hospital of Padua, Italy, from 1998 to 2022, were included.</p></div><div><h3>Results</h3><p>No difference in the occurrence of cirrhosis decompensating events and development of hepatocellular carcinoma was observed, whereas patients in the MASLD or mixed group had 4-3-fold higher all-cause mortality and significantly lower 3-years survival compared to patients with non-MASLD cirrhosis, despite a better liver function at enrolment. Hypertriglyceridemia and low HDL levels were the less prevalent cardiometabolic factors, but those associated with the highest risk of cirrhosis decompensation. Hypertriglyceridemia was also associated with an increased risk of mortality. Arterial hypertension was associated with a reduced risk of cirrhosis decompensation, but a higher risk of mortality.</p></div><div><h3>Conclusion</h3><p>Compared to patients with non-MASLD cirrhosis, those with cardiometabolic risk factors had similar rates of liver cirrhosis decompensation but higher overall mortality. Hypertriglyceridemia was associated with a high risk of both liver decompensation and death.</p></div>\",\"PeriodicalId\":11268,\"journal\":{\"name\":\"Digestive and Liver Disease\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Digestive and Liver Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S159086582400937X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Digestive and Liver Disease","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S159086582400937X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
Cardiometabolic risk factors and clinical course of liver cirrhosis
Introduction
The global prevalence of Metabolic Dysfunction-Associated Liver Disease (MASLD) is dramatically increasing with the diffusion of cardiometabolic risk factors. The aim of the present study was to assess the natural course of liver cirrhosis, in terms of decompensation, development of hepatocellular carcinoma and mortality, in relation to the presence of cardiometabolic risk factors (type 2 diabetes mellitus, obesity, arterial hypertension, low HDL levels, hypertriglyceridemia). Patients: 667 patients with liver cirrhosis (50 with MASLD aetiology, 167 with non-MASLD aetiology, and 450 with a non-MASLD etiological factor plus the presence of at least one cardiometabolic risk factor) followed at the University and General Hospital of Padua, Italy, from 1998 to 2022, were included.
Results
No difference in the occurrence of cirrhosis decompensating events and development of hepatocellular carcinoma was observed, whereas patients in the MASLD or mixed group had 4-3-fold higher all-cause mortality and significantly lower 3-years survival compared to patients with non-MASLD cirrhosis, despite a better liver function at enrolment. Hypertriglyceridemia and low HDL levels were the less prevalent cardiometabolic factors, but those associated with the highest risk of cirrhosis decompensation. Hypertriglyceridemia was also associated with an increased risk of mortality. Arterial hypertension was associated with a reduced risk of cirrhosis decompensation, but a higher risk of mortality.
Conclusion
Compared to patients with non-MASLD cirrhosis, those with cardiometabolic risk factors had similar rates of liver cirrhosis decompensation but higher overall mortality. Hypertriglyceridemia was associated with a high risk of both liver decompensation and death.
期刊介绍:
Digestive and Liver Disease is an international journal of Gastroenterology and Hepatology. It is the official journal of Italian Association for the Study of the Liver (AISF); Italian Association for the Study of the Pancreas (AISP); Italian Association for Digestive Endoscopy (SIED); Italian Association for Hospital Gastroenterologists and Digestive Endoscopists (AIGO); Italian Society of Gastroenterology (SIGE); Italian Society of Pediatric Gastroenterology and Hepatology (SIGENP) and Italian Group for the Study of Inflammatory Bowel Disease (IG-IBD).
Digestive and Liver Disease publishes papers on basic and clinical research in the field of gastroenterology and hepatology.
Contributions consist of:
Original Papers
Correspondence to the Editor
Editorials, Reviews and Special Articles
Progress Reports
Image of the Month
Congress Proceedings
Symposia and Mini-symposia.