MAFLD, patient-centred care, and APASL

被引:0
作者
Shiv K. Sarin
Mohammed Eslam
Jian-Gao Fan
Han-Chieh Lin
Jacob George
Masao Omata
机构
[1] Institute of Liver and Biliary Sciences,Department of Hepatology
[2] Westmead Hospital and University of Sydney,Storr Liver Centre, Westmead Institute for Medical Research
[3] Shanghai Jiao Tong University School of Medicine,Department of Gastroenterology, Xinhua Hospital
[4] Taipei Veterans General Hospital,Division of Gastroenterology and Hepatology, Department of Medicine
[5] Yamanashi Prefectural Central Hospital,Department of Gastroenterology
[6] The University of Tokyo,undefined
来源
Hepatology International | 2022年 / 16卷
关键词
MAFLD; APASL; Patient-centred care; Clinical trials;
D O I
暂无
中图分类号
学科分类号
摘要
Asian–Pacific nations are home to more than half the world’s population and similar to other global super regions, metabolic dysfunction associated fatty liver disease (MAFLD) is the principal cause for chronic liver disease. To address the challenges ahead for tackling the disease at-scale, the Asian Pacific Association for the Study of the Liver (APASL) was the first pan-national society to endorse and lead the process for redefining the disease and adopting the more appropriate term “MAFLD” with its accompanying set of positive diagnostic criteria. As with this initiative, APASL and Hepatology International will continue to strive to lead the field and work with sister societies towards full adoption of MAFLD. This will advance the science and practice of Hepatology and help incorporate MAFLD within multidisciplinary care teams. Ultimately, it will lead to more cogent clinical trials built on innovative design platforms that include patients with any disease related to metabolic dysfunction. For our patients, an outcome of these endeavours will be the provision of holistic person-centred care for this disease that is so common in our region.
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页码:1032 / 1034
页数:2
相关论文
共 145 条
[1]  
Sarin SK(2020)Liver diseases in the Asia–Pacific region: a lancet gastroenterology & hepatology commission Lancet Gastroenterol Hepatol 5 167-228
[2]  
Kumar M(2022)Estimating global prevalence of metabolic dysfunction-associated fatty liver disease in overweight or obese adults Clin Gastroenterol Hepatol 20 e573-e582
[3]  
Eslam M(2020)The Asian Pacific Association for the Study of the Liver clinical practice guidelines for the diagnosis and management of metabolic associated fatty liver disease Hepatol Int 14 889-919
[4]  
George J(2022)Global prevalence and clinical characteristics of metabolic associated fatty liver disease. A meta-analysis and systematic review of 10,739,607 individuals J Clin Endocrinol Metab 107 2691-2700
[5]  
Al Mahtab M(2019)Genetic insights for drug development in NAFLD Trends Pharmacol Sci 40 506-516
[6]  
Akbar SMF(2021)Redefining fatty liver disease: an international patient perspective Lancet Gastroenterol Hepatol 6 73-79
[7]  
Jia J(2020)MAFLD: a consensus-driven proposed nomenclature for metabolic associated fatty liver disease Gastroenterology 158 1999-2014
[8]  
Liu J(2020)A new definition for metabolic dysfunction-associated fatty liver disease: an international expert consensus statement J Hepatol 73 202-209
[9]  
Ayada I(2021)Defining paediatric metabolic (dysfunction)-associated fatty liver disease: an international expert consensus statement Lancet Gastroenterol Hepatol 6 864-873
[10]  
Zhang X(2017)Metabolic syndrome and severity of fibrosis in nonalcoholic fatty liver disease: an age-dependent risk profiling study Liver Int 37 1389-1396