Cargando…

Nonalcoholic fatty liver disease shows significant sex dimorphism

Nonalcoholic fatty liver disease (NAFLD), which has been renamed metabolic dysfunction-associated fatty liver disease, is a growing global medical problem. The incidence of NAFLD and its associated end-stage liver disease is increasing each year, and many research advancements have been achieved to...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Xing-Yu, Wang, Cong, Huang, Yi-Zhou, Zhang, Li-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855265/
https://www.ncbi.nlm.nih.gov/pubmed/35211584
http://dx.doi.org/10.12998/wjcc.v10.i5.1457
_version_ 1784653617921261568
author Chen, Xing-Yu
Wang, Cong
Huang, Yi-Zhou
Zhang, Li-Li
author_facet Chen, Xing-Yu
Wang, Cong
Huang, Yi-Zhou
Zhang, Li-Li
author_sort Chen, Xing-Yu
collection PubMed
description Nonalcoholic fatty liver disease (NAFLD), which has been renamed metabolic dysfunction-associated fatty liver disease, is a growing global medical problem. The incidence of NAFLD and its associated end-stage liver disease is increasing each year, and many research advancements have been achieved to date. This review focuses on the current knowledge of the sex differences in NAFLD and does not elaborate on areas without differences. Studies have revealed significant sex differences in the prevalence, influencing factors, pathophysiology, complications and therapies of NAFLD. Men have a higher incidence than women. Compared with women, men exhibit increased visceral fat deposition, are more susceptible to leptin resistance, lack estrogen receptors, and tend to synthesize fatty acids into fat storage. Male patients will experience more severe hepatic fibrosis and a higher incidence of liver cancer. However, once NAFLD occurs, women show a faster progression of liver fibrosis, higher levels of liver cell damage and inflammation and are less likely to undergo liver transplantation than men. In general, men have more risk factors and more severe pathophysiological reactions than women, whereas the development of NAFLD is faster in women, and the treatments for women are more limited than those for men. Thus, whether sex differences should be considered in the individualized prevention and treatment of NAFLD in the future is worth considering.
format Online
Article
Text
id pubmed-8855265
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Baishideng Publishing Group Inc
record_format MEDLINE/PubMed
spelling pubmed-88552652022-02-23 Nonalcoholic fatty liver disease shows significant sex dimorphism Chen, Xing-Yu Wang, Cong Huang, Yi-Zhou Zhang, Li-Li World J Clin Cases Review Nonalcoholic fatty liver disease (NAFLD), which has been renamed metabolic dysfunction-associated fatty liver disease, is a growing global medical problem. The incidence of NAFLD and its associated end-stage liver disease is increasing each year, and many research advancements have been achieved to date. This review focuses on the current knowledge of the sex differences in NAFLD and does not elaborate on areas without differences. Studies have revealed significant sex differences in the prevalence, influencing factors, pathophysiology, complications and therapies of NAFLD. Men have a higher incidence than women. Compared with women, men exhibit increased visceral fat deposition, are more susceptible to leptin resistance, lack estrogen receptors, and tend to synthesize fatty acids into fat storage. Male patients will experience more severe hepatic fibrosis and a higher incidence of liver cancer. However, once NAFLD occurs, women show a faster progression of liver fibrosis, higher levels of liver cell damage and inflammation and are less likely to undergo liver transplantation than men. In general, men have more risk factors and more severe pathophysiological reactions than women, whereas the development of NAFLD is faster in women, and the treatments for women are more limited than those for men. Thus, whether sex differences should be considered in the individualized prevention and treatment of NAFLD in the future is worth considering. Baishideng Publishing Group Inc 2022-02-16 2022-02-16 /pmc/articles/PMC8855265/ /pubmed/35211584 http://dx.doi.org/10.12998/wjcc.v10.i5.1457 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Review
Chen, Xing-Yu
Wang, Cong
Huang, Yi-Zhou
Zhang, Li-Li
Nonalcoholic fatty liver disease shows significant sex dimorphism
title Nonalcoholic fatty liver disease shows significant sex dimorphism
title_full Nonalcoholic fatty liver disease shows significant sex dimorphism
title_fullStr Nonalcoholic fatty liver disease shows significant sex dimorphism
title_full_unstemmed Nonalcoholic fatty liver disease shows significant sex dimorphism
title_short Nonalcoholic fatty liver disease shows significant sex dimorphism
title_sort nonalcoholic fatty liver disease shows significant sex dimorphism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855265/
https://www.ncbi.nlm.nih.gov/pubmed/35211584
http://dx.doi.org/10.12998/wjcc.v10.i5.1457
work_keys_str_mv AT chenxingyu nonalcoholicfattyliverdiseaseshowssignificantsexdimorphism
AT wangcong nonalcoholicfattyliverdiseaseshowssignificantsexdimorphism
AT huangyizhou nonalcoholicfattyliverdiseaseshowssignificantsexdimorphism
AT zhanglili nonalcoholicfattyliverdiseaseshowssignificantsexdimorphism