{"title":"Metabolic associated fatty liver disease and sarcopenia additively increase mortality: a real-world study.","authors":"Qianwen Zhao, Yifan Yin, Yunlei Deng","doi":"10.1038/s41387-023-00250-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and aims: </strong>Sarcopenia is associated with worse prognosis for non-alcoholic fatty liver disease (NAFLD). However, disease progression in the MAFLD-related sarcopenia is largely unknown. We aimed to clarify the relationship between MAFLD and/or sarcopenia with mortality and liver fibrosis in the real world.</p><p><strong>Methods: </strong>A total of 13,692 individuals were selected from the third National Health and Nutrition Examination Surveys and linked mortality until December 2019. MAFLD is diagnosed based on a radiologically diagnosed hepatic steatosis and the presence of any one of the following three conditions: overweight/obesity, diabetes mellitus (DM), or metabolic dysregulation. Sarcopenia is defined by weight-adjusted skeletal muscle mass.</p><p><strong>Results: </strong>The mean age was 43.7 ± 15.97 years, and 47.3% of the individuals were male. MAFLD was diagnosed in 4207/13,692 (30.73%) participants, and the proportion of sarcopenic was 19.42% amongst subjects with MAFLD. The mean follow-up duration was of 23.7 ± 7.62 years. MAFLD (aHR 1.152, 95% CI 1.070-1.241) and sarcopenia (aHR 1.123, 95% CI 1.042-1.210) were related to increased all-cause mortality in MAFLD after adjustment for age, sex, race, marital status, education, and smoking. Stratified analysis revealed that MAFLD and sarcopenia additively increased the risk of mortality (aHR 1.247, 95% CI 1.132-1.373) and liver fibrosis (aOR 2.296, 95% CI 1.718-3.069 assessed by NFS score >0.676; aOR 2.218, 95% CI 1.788-2.752 assessed by FIB-4 score >1.3) in fully adjusted models (P < 0.001 for all).</p><p><strong>Conclusion: </strong>Sarcopenia in individuals with MAFLD portends increased mortality and significant liver fibrosis. Novel therapeutic strategies targeting at increasing skeletal muscle mass should be explored for patients with MAFLD.</p>","PeriodicalId":19339,"journal":{"name":"Nutrition & Diabetes","volume":"13 1","pages":"21"},"PeriodicalIF":4.6000,"publicationDate":"2023-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651884/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nutrition & Diabetes","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41387-023-00250-6","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Background and aims: Sarcopenia is associated with worse prognosis for non-alcoholic fatty liver disease (NAFLD). However, disease progression in the MAFLD-related sarcopenia is largely unknown. We aimed to clarify the relationship between MAFLD and/or sarcopenia with mortality and liver fibrosis in the real world.
Methods: A total of 13,692 individuals were selected from the third National Health and Nutrition Examination Surveys and linked mortality until December 2019. MAFLD is diagnosed based on a radiologically diagnosed hepatic steatosis and the presence of any one of the following three conditions: overweight/obesity, diabetes mellitus (DM), or metabolic dysregulation. Sarcopenia is defined by weight-adjusted skeletal muscle mass.
Results: The mean age was 43.7 ± 15.97 years, and 47.3% of the individuals were male. MAFLD was diagnosed in 4207/13,692 (30.73%) participants, and the proportion of sarcopenic was 19.42% amongst subjects with MAFLD. The mean follow-up duration was of 23.7 ± 7.62 years. MAFLD (aHR 1.152, 95% CI 1.070-1.241) and sarcopenia (aHR 1.123, 95% CI 1.042-1.210) were related to increased all-cause mortality in MAFLD after adjustment for age, sex, race, marital status, education, and smoking. Stratified analysis revealed that MAFLD and sarcopenia additively increased the risk of mortality (aHR 1.247, 95% CI 1.132-1.373) and liver fibrosis (aOR 2.296, 95% CI 1.718-3.069 assessed by NFS score >0.676; aOR 2.218, 95% CI 1.788-2.752 assessed by FIB-4 score >1.3) in fully adjusted models (P < 0.001 for all).
Conclusion: Sarcopenia in individuals with MAFLD portends increased mortality and significant liver fibrosis. Novel therapeutic strategies targeting at increasing skeletal muscle mass should be explored for patients with MAFLD.
背景和目的:肌少症与非酒精性脂肪性肝病(NAFLD)预后不良相关。然而,与mafld相关的肌肉减少症的疾病进展在很大程度上是未知的。我们的目的是澄清现实世界中MAFLD和/或肌肉减少症与死亡率和肝纤维化之间的关系。方法:从截至2019年12月的第三次全国健康与营养检查调查和相关死亡率中选择了13692人。MAFLD的诊断基于影像学诊断的肝脂肪变性和以下三种情况中的任何一种:超重/肥胖、糖尿病(DM)或代谢失调。肌肉减少症的定义是体重调整后的骨骼肌质量。结果:平均年龄43.7±15.97岁,男性占47.3%。4207/ 13692名参与者(30.73%)被诊断为MAFLD,其中肌肉减少的比例为19.42%。平均随访时间23.7±7.62年。经年龄、性别、种族、婚姻状况、教育程度和吸烟调整后,MAFLD (aHR 1.152, 95% CI 1.070-1.241)和肌肉减少症(aHR 1.123, 95% CI 1.042-1.210)的全因死亡率增加相关。分层分析显示,MAFLD和肌肉减少症增加了死亡率(aHR 1.247, 95% CI 1.132-1.373)和肝纤维化(aOR 2.296, 95% CI 1.718-3.069, NFS评分>0.676)的风险;aOR 2.218, 95% CI 1.788-2.752 (FIB-4评分>1.3)。结论:肌少症患者的死亡率增加,肝纤维化显著。针对增加骨骼肌质量的新治疗策略应用于MAFLD患者的探索。
期刊介绍:
Nutrition & Diabetes is a peer-reviewed, online, open access journal bringing to the fore outstanding research in the areas of nutrition and chronic disease, including diabetes, from the molecular to the population level.