Alcohol-associated liver disease increases the risk of muscle loss and mortality in patients with cirrhosis

IF 6.9 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Journal of Gastroenterology Pub Date : 2024-07-28 DOI:10.1007/s00535-024-02137-4
Tatsunori Hanai, Kayoko Nishimura, Shinji Unome, Takao Miwa, Yuki Nakahata, Kenji Imai, Atsushi Suetsugu, Koji Takai, Masahito Shimizu
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Abstract

Background

Rapid skeletal muscle loss adversely affects the clinical outcomes of liver cirrhosis. However, the relationships between the annual changes in skeletal muscle area (ΔSMA/year) and the etiology of cirrhosis, factors associated with muscle loss, and risk of mortality remains unclear.

Methods

A total of 384 patients who underwent multiple computed tomography (CT) scans between March 2004 and June 2021 were enrolled in this study (median age, 67 years; 64% men; median model for end-stage liver disease score, 9). Body composition and ΔSMA/year were estimated using a 3D image analysis system and data from at least two distinct CT scans. Differences in ΔSMA/year among different etiologies of cirrhosis, factors associated with rapid muscle loss (defined as ΔSMA/year ≤ − 3.1%), and the association between ΔSMA/year and mortality were examined.

Results

Patients with alcohol-associated liver disease (ALD) cirrhosis experienced more rapid muscle loss (ΔSMA/year, − 5.7%) than those with hepatitis B (ΔSMA/year, − 2.8%) and hepatitis C cirrhosis (ΔSMA/year, − 3.1%). ALD cirrhosis was independently associated with ΔSMA/year ≤ − 3.1% after adjusting for age, sex, and liver functional reserve. Over a median follow-up period of 3.8 years, ALD cirrhosis, ΔSMA/year ≤ − 3.1%, and low subcutaneous adipose tissue level were found to be significantly associated with reduced survival. ALD cirrhosis (hazard ratio [HR], 2.43; 95% confidence interval [CI] 1.12–5.28) and ΔSMA/year ≤ − 3.1% (HR, 3.68; 95% CI 2.46–5.52) were also predictive of mortality.

Conclusions

These results suggest that ALD cirrhosis increases the risk of rapid muscle loss and mortality in affected patients.

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酒精相关肝病会增加肝硬化患者肌肉萎缩和死亡的风险
背景骨骼肌的快速流失会对肝硬化的临床结果产生不利影响。本研究共纳入了 384 名在 2004 年 3 月至 2021 年 6 月期间接受过多次计算机断层扫描(CT)的患者(中位年龄 67 岁;64% 为男性;中位终末期肝病模型评分 9 分)。身体成分和ΔSMA/年是通过三维图像分析系统和至少两次不同的CT扫描数据估算出来的。研究了不同病因肝硬化患者的ΔSMA/年差异、肌肉快速流失的相关因素(定义为ΔSMA/年≤ - 3.1%)以及ΔSMA/年与死亡率之间的关系。结果与乙型肝炎(ΔSMA/年,- 2.8%)和丙型肝炎肝硬化(ΔSMA/年,- 3.1%)患者相比,酒精相关性肝病(ALD)肝硬化患者的肌肉流失速度更快(ΔSMA/年,- 5.7%)。在对年龄、性别和肝功能储备进行调整后,ALD肝硬化与ΔSMA/年≤-3.1%独立相关。在中位 3.8 年的随访期间,发现 ALD 肝硬化、ΔSMA/年≤ - 3.1%、皮下脂肪组织水平低与存活率降低显著相关。ALD 肝硬化(危险比 [HR],2.43;95% 置信区间 [CI],1.12-5.28)和 ΔSMA/year ≤ - 3.1%(HR,3.68;95% 置信区间 [CI],2.46-5.52)也可预测死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Gastroenterology
Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
12.20
自引率
1.60%
发文量
99
审稿时长
4-8 weeks
期刊介绍: The Journal of Gastroenterology, which is the official publication of the Japanese Society of Gastroenterology, publishes Original Articles (Alimentary Tract/Liver, Pancreas, and Biliary Tract), Review Articles, Letters to the Editors and other articles on all aspects of the field of gastroenterology. Significant contributions relating to basic research, theory, and practice are welcomed. These publications are designed to disseminate knowledge in this field to a worldwide audience, and accordingly, its editorial board has an international membership.
期刊最新文献
Publisher Correction: CRAFITY score as a predictive marker for refractoriness to atezolizumab plus bevacizumab therapy in hepatocellular carcinoma: a multicenter retrospective study. Alcohol-associated liver disease increases the risk of muscle loss and mortality in patients with cirrhosis. Small extracellular vesicles derived from adipose mesenchymal stem cells alleviate intestinal fibrosis by inhibiting the FAK/Akt signaling pathway via MFGE8. Response to letter to the editor regarding: "Alcohol-associated liver disease increases the risk of muscle reduction and mortality in patients with cirrhosis". Association of circulating cytokine levels and tissue-infiltrating myeloid cells with achalasia: results from Mendelian randomization and validation through clinical characteristics and single-cell RNA sequencing.
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