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肝脂肪变中的肌少症性肥胖。

Sarcopenic obesity in fatty liver.

机构信息

Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.

出版信息

Curr Opin Clin Nutr Metab Care. 2019 May;22(3):185-190. doi: 10.1097/MCO.0000000000000558.

Abstract

PURPOSE OF REVIEW

Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steato hepatitis have an increasing prevalence among liver diseases. Overweight and obesity are frequently associated conditions in patients with fatty liver. Skeletal muscle mass depletion may also coexist with chronic liver disease even in obese patients. This review will focus on the relationship between sarcopenic obesity and fatty liver.

RECENT FINDINGS

Obesity and sarcopenia are frequently encountered in patients with NAFLD. Adipose tissue is able to release molecules (adipokines) that regulate lipid metabolism, interact with insulin sensitivity and may contribute to induce fibrogenesis in the liver. Skeletal muscle tissue is able to secrete myokines regulating muscle metabolism and insulin sensitivity. Myokines perturbation has been reported to influence adipose tissue mass and fat deposition in the liver. Sarcopenia has been reported as independent risk factor for the development of NAFLD, and for a more severe liver fibrosis in patients with NAFLD.

SUMMARY

The interaction between skeletal muscle, adipose tissue and the liver may play a role in the development of NAFLD. Sarcopenia and sarcopenic obesity are risk factors for the development of fatty liver and associated with more severe liver fibrosis. Management is not standardized, but dietary counseling and physical training have been proposed as promising strategies. Bariatric surgery may be considered in patients with severe 'resistant' obesity.

摘要

目的综述

非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎在肝脏疾病中的发病率不断上升。超重和肥胖是脂肪性肝病患者常见的伴随疾病。即使在肥胖患者中,慢性肝病也可能伴有骨骼肌质量耗竭。本文将重点讨论肌少性肥胖与脂肪肝的关系。

最新研究发现

NAFLD 患者常伴有肥胖和肌少症。脂肪组织能够释放调节脂质代谢的分子(脂肪因子),与胰岛素敏感性相互作用,并可能导致肝脏纤维化。骨骼肌组织能够分泌调节肌肉代谢和胰岛素敏感性的肌因子。肌因子的紊乱被报道会影响脂肪组织质量和肝脏脂肪沉积。肌少症已被报道为 NAFLD 发展的独立危险因素,也是 NAFLD 患者更严重肝纤维化的危险因素。

总结

骨骼肌、脂肪组织和肝脏之间的相互作用可能在 NAFLD 的发生发展中起作用。肌少症和肌少性肥胖是脂肪肝发展的危险因素,并与更严重的肝纤维化相关。管理尚未标准化,但已提出饮食咨询和身体锻炼是有前途的策略。对于严重的“抵抗性”肥胖患者,可能需要考虑进行减重手术。

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