Metabolic dysfunction-associated steatotic liver disease in adults.

IF 76.9 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Daniel Q Huang, Vincent W S Wong, Mary E Rinella, Jerome Boursier, Jeffrey V Lazarus, Hannele Yki-Järvinen, Rohit Loomba
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引用次数: 0

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the umbrella term that comprises metabolic dysfunction-associated steatotic liver, or isolated hepatic steatosis, through to metabolic dysfunction-associated steatohepatitis, the progressive necroinflammatory disease form that can progress to fibrosis, cirrhosis and hepatocellular carcinoma. MASLD is estimated to affect more than one-third of adults worldwide. MASLD is closely associated with insulin resistance, obesity, gut microbial dysbiosis and genetic risk factors. The obesity epidemic and the growing prevalence of type 2 diabetes mellitus greatly contribute to the increasing burden of MASLD. The treatment and prevention of major metabolic comorbidities such as type 2 diabetes mellitus and obesity will probably slow the growth of MASLD. In 2023, the field decided on a new nomenclature and agreed on a set of research and action priorities, and in 2024, the US FDA approved the first drug, resmetirom, for the treatment of non-cirrhotic metabolic dysfunction-associated steatohepatitis with moderate to advanced fibrosis. Reliable, validated biomarkers that can replace histology for patient selection and primary end points in MASH trials will greatly accelerate the drug development process. Additionally, noninvasive tests that can reliably determine treatment response or predict response to therapy are warranted. Sustained efforts are required to combat the burden of MASLD by tackling metabolic risk factors, improving risk stratification and linkage to care, and increasing access to therapeutic agents and non-pharmaceutical interventions.

成人代谢功能障碍相关的脂肪变性肝病
代谢功能障碍相关的脂肪变性肝病(MASLD)是一个总称,包括代谢功能障碍相关的脂肪变性肝或孤立性肝脂肪变性,以及代谢功能障碍相关的脂肪性肝炎,这是一种进行性坏死炎症性疾病,可发展为纤维化、肝硬化和肝细胞癌。据估计,全球超过三分之一的成年人受到MASLD的影响。MASLD与胰岛素抵抗、肥胖、肠道微生物失调和遗传危险因素密切相关。肥胖的流行和2型糖尿病的日益流行极大地促进了MASLD负担的增加。治疗和预防主要的代谢合并症,如2型糖尿病和肥胖,可能会减缓MASLD的生长。2023年,该领域决定了一个新的命名法,并就一系列研究和行动重点达成了一致。2024年,美国FDA批准了首个药物resmetirom,用于治疗非肝硬化代谢功能障碍相关脂肪性肝炎伴中晚期纤维化。可靠的、经过验证的生物标志物可以取代组织学,在MASH试验中选择患者和主要终点,这将大大加快药物开发过程。此外,可以可靠地确定治疗反应或预测治疗反应的无创测试是必要的。需要通过处理代谢风险因素、改善风险分层和与护理的联系以及增加获得治疗剂和非药物干预措施的机会,持续努力减轻MASLD的负担。
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来源期刊
Nature Reviews Disease Primers
Nature Reviews Disease Primers Medicine-General Medicine
CiteScore
76.70
自引率
0.20%
发文量
75
期刊介绍: Nature Reviews Disease Primers, a part of the Nature Reviews journal portfolio, features sections on epidemiology, mechanisms, diagnosis, management, and patient quality of life. The editorial team commissions top researchers — comprising basic scientists and clinical researchers — to write the Primers, which are designed for use by early career researchers, medical students and principal investigators. Each Primer concludes with an Outlook section, highlighting future research directions. Covered medical specialties include Cardiology, Dermatology, Ear, Nose and Throat, Emergency Medicine, Endocrinology, Gastroenterology, Genetic Conditions, Gynaecology and Obstetrics, Hepatology, Haematology, Infectious Diseases, Maxillofacial and Oral Medicine, Nephrology, Neurology, Nutrition, Oncology, Ophthalmology, Orthopaedics, Psychiatry, Respiratory Medicine, Rheumatology, Sleep Medicine, and Urology.
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