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Association of metabolic dysfunction-associated fatty liver disease with kidney disease

Association of metabolic dysfunction-associated fatty liver disease with kidney disease
Association of metabolic dysfunction-associated fatty liver disease with kidney disease
Non-alcoholic fatty liver disease (NAFLD) is characterized by the accumulation of fat in more than 5% of hepatocytes in the absence of excessive alcohol consumption and other secondary causes of hepatic steatosis. In 2020, the more inclusive term metabolic (dysfunction)-associated fatty liver disease (MAFLD) — defined by broader diagnostic criteria — was proposed to replace the term NAFLD. The new terminology and revised definition better emphasize the pathogenic role of metabolic dysfunction and uses a set of definitive, inclusive criteria for diagnosis. Diagnosis of MAFLD is based on evidence of hepatic steatosis (as assessed by liver biopsy, imaging techniques or blood biomarkers and scores) in persons who are overweight or obese and have type 2 diabetes mellitus or metabolic dysregulation, regardless of the coexistence of other liver diseases or excessive alcohol consumption. The known association between NAFLD and chronic kidney disease (CKD) and our understanding that CKD can occur as a consequence of metabolic dysfunction suggests that individuals with MAFLD — who by definition have fatty liver and metabolic comorbidities — are at increased risk of CKD. In this Perspective article, we discuss the clinical associations between MAFLD and CKD, the pathophysiological mechanisms by which MAFLD may increase the risk of CKD and the potential drug treatments that may benefit both conditions.
1759-5061
259-268
Wang, Ting-Yao
0f8d497a-5ec5-442e-887f-192799433d96
Wang, Rui-Fang
26bae82b-0d09-4883-8fa5-cfd5a2c9d2f0
Bu, Zhi-Yin
493d757b-0660-4616-9933-249aef124039
Targher, Giovanni
043e0811-b389-4922-974e-22e650212c5f
Byrne, Christopher
1370b997-cead-4229-83a7-53301ed2a43c
Sun, Dan-Qin
476ddf44-9f7a-4581-80f2-3fecf991f7d9
Zheng, Ming-Hua
3190b58b-12a4-4d89-9a4b-b48902cd795e
Wang, Ting-Yao
0f8d497a-5ec5-442e-887f-192799433d96
Wang, Rui-Fang
26bae82b-0d09-4883-8fa5-cfd5a2c9d2f0
Bu, Zhi-Yin
493d757b-0660-4616-9933-249aef124039
Targher, Giovanni
043e0811-b389-4922-974e-22e650212c5f
Byrne, Christopher
1370b997-cead-4229-83a7-53301ed2a43c
Sun, Dan-Qin
476ddf44-9f7a-4581-80f2-3fecf991f7d9
Zheng, Ming-Hua
3190b58b-12a4-4d89-9a4b-b48902cd795e

Wang, Ting-Yao, Wang, Rui-Fang, Bu, Zhi-Yin, Targher, Giovanni, Byrne, Christopher, Sun, Dan-Qin and Zheng, Ming-Hua (2022) Association of metabolic dysfunction-associated fatty liver disease with kidney disease. Nature Reviews Nephrology, 18 (4), 259-268. (doi:10.1038/s41581-021-00519-y).

Record type: Article

Abstract

Non-alcoholic fatty liver disease (NAFLD) is characterized by the accumulation of fat in more than 5% of hepatocytes in the absence of excessive alcohol consumption and other secondary causes of hepatic steatosis. In 2020, the more inclusive term metabolic (dysfunction)-associated fatty liver disease (MAFLD) — defined by broader diagnostic criteria — was proposed to replace the term NAFLD. The new terminology and revised definition better emphasize the pathogenic role of metabolic dysfunction and uses a set of definitive, inclusive criteria for diagnosis. Diagnosis of MAFLD is based on evidence of hepatic steatosis (as assessed by liver biopsy, imaging techniques or blood biomarkers and scores) in persons who are overweight or obese and have type 2 diabetes mellitus or metabolic dysregulation, regardless of the coexistence of other liver diseases or excessive alcohol consumption. The known association between NAFLD and chronic kidney disease (CKD) and our understanding that CKD can occur as a consequence of metabolic dysfunction suggests that individuals with MAFLD — who by definition have fatty liver and metabolic comorbidities — are at increased risk of CKD. In this Perspective article, we discuss the clinical associations between MAFLD and CKD, the pathophysiological mechanisms by which MAFLD may increase the risk of CKD and the potential drug treatments that may benefit both conditions.

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Accepted/In Press date: 20 July 2021
e-pub ahead of print date: 10 January 2022
Published date: 1 April 2022
Additional Information: Funding Information: The authors’ work was supported by grants from the National Natural Science Foundation of China (82070588, 82000690), High Level Creative Talents from the Department of Public Health in Zhejiang Province, Project of New Century 551 Talent Nurturing in Wenzhou and a Project of Science and Technology Development Fund in Wuxi (N20202001). D.-Q.S. is supported in part by grants from the Youth Research Project Fund from Wuxi Municipal Health Commission (Q201932), Top-notch Talents from Young and Middle-Age Health Care in Wuxi (BJ2020026). G.T. is supported in part by grants from the University School of Medicine of Verona, Verona, Italy. C.D.B. is supported in part by the Southampton NIHR Biomedical Research Centre (IS-BRC-20004), UK. Publisher Copyright: © 2022, Springer Nature Limited.

Identifiers

Local EPrints ID: 450477
URI: http://eprints.soton.ac.uk/id/eprint/450477
ISSN: 1759-5061
PURE UUID: 7c607880-c472-4d5c-8621-b551c6426947
ORCID for Christopher Byrne: ORCID iD orcid.org/0000-0001-6322-7753

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Date deposited: 29 Jul 2021 16:31
Last modified: 17 Mar 2024 06:43

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Contributors

Author: Ting-Yao Wang
Author: Rui-Fang Wang
Author: Zhi-Yin Bu
Author: Giovanni Targher
Author: Dan-Qin Sun
Author: Ming-Hua Zheng

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