TY - JOUR
T1 - Metabolic Associated Fatty Liver Disease Increases the Risk of Systemic Complications and Mortality. A Meta-Analysis and Systematic Review of 12 620 736 Individuals
AU - Quek, Jingxuan
AU - Ng, Cheng Han
AU - Tang, Ansel Shao Pin
AU - Chew, Nicholas
AU - Chan, Mark
AU - Khoo, Chin Meng
AU - Wei, Chen Poh
AU - Chin, Yip Han
AU - Tay, Phoebe
AU - Lim, Grace
AU - Tan, Darren Jun Hao
AU - Lim, Wen Hui
AU - Chan, Kai En
AU - Teng, Margaret
AU - Tan, Eunice
AU - Tamaki, Nobuharu
AU - Huang, Daniel Q.
AU - Siddiqui, Mohammad Shadab
AU - Young, Dan Yock
AU - Noureddin, Mazen
AU - Muthiah, Mark D.
N1 - Funding Information:
All authors have made substantial contributions to all of the following: (1) the conception and design of the study, or acquisition of data, or analysis and interpretation of data, (2) drafting the article or revising it critically for important intellectual content, (3) final approval of the version to be submitted. No writing assistance was obtained in the preparation of the manuscript. The manuscript, including related data, figures, and tables has not been previously published, and the manuscript is not under consideration elsewhere. All articles in this manuscript are available from MEDLINE and Embase. The study was conducted in accordance with the Declaration of Helsinki. The study was exempt from IRB review was no confidential patient information was involved. C.H.N. M.T. E.T. and M.D.M. conceptualized the study; C.H.N. J.Q. A.S.P.T. N.C. M.T. and E.T. curated the data; C.H.N. J.Q. A.S.P.T. N.C. M.C. C.M.K. C.P.W. Y.H.C. G.L. D.J.H.T. and W.H.L. performed the formal analysis; N.T. D.Q.H. M.S.S. M.N. and M.D.M. supervised the study; C.H.N. J.Q. A.S.P.T. N.C. M.C. C.M.K. C.P.W. Y.H.C. G.L. M.T. E.T. P.T. D.J.H.T. W.H.L. N.T. D.Q.H. M.S.S. M.N. and M.D.M. validated the study; C.H.N. J.Q. A.S.P.T. and N.C. wrote the original draft; and C.H.N. J.Q. A.S.P.T. N.C. M.C. C.M.K. C.P.W. Y.H.C. G.L. D.J.H.T. W.H.L. P.T. N.T. D.Q.H. M.S.S. M.N. and M.D.M. were involved in writing, review, and editing. J.Q. C.H.N. and A.S.P.T. contributed equally. M.N. and M.D.M. equally supervised the study. All authors have read and approved the final version of the manuscript for submission. M.N. has been on the advisory board for 89BIO, Gilead, Intercept, Pfizer, Novo Nordisk, Blade, EchoSens, Fractyl, Terns, Siemens, and Roche diagnostic; M.N. has received research support from Allergan, BMS, Gilead, Galmed, Galectin, Genfit, Conatus, Enanta, Madrigal, Novartis, Pfizer, Shire, Viking, and Zydus; M.N. is a minor shareholder or has stocks in Anaetos, Rivus Pharma, and Viking. All other authors have no multiplicity of interest to disclose.
Publisher Copyright:
© 2022 AACE
PY - 2022/7
Y1 - 2022/7
N2 - Objective: The recent introduction of the term metabolic associated fatty liver disease (MAFLD) sought to reclassify nonalcoholic fatty liver disease (NAFLD). MAFLD is thought to improve the encapsulation of metabolic dysregulation. However, recent evidence has found significant differences between MAFLD and NAFLD, and prevailing knowledge has largely arisen from studies on NAFLD. Hence, we conducted a meta-analysis and systematic review of the outcomes associated with MAFLD. Methods: MEDLINE and Embase databases were searched for articles relating to outcomes in MAFLD. Analysis was conducted in random effects with hazard ratios (HRs) to account for longitudinal risk assessment of mortality and systemic complications. Results: A total of 554 articles were identified, of which 17 articles were included. MAFLD resulted in an increase in the overall mortality (HR, 1.24; confidence interval [CI], 1.13-1.34), cancer-related mortality (HR, 1.27; CI, 1.01-1.54), and cardiovascular disease mortality (HR, 1.28, 1.03-1.53; P =.04) compared with non-MAFLD. MAFLD also increases the risk of cardiovascular events (HR, 1.49; CI, 1.34-1.64; P <.01), stroke (HR, 1.55; CI, 1.37-1.73; P <.01), and chronic kidney disease (HR, 1.53; CI, 1.38-1.68). The presence of MAFLD was also associated with an increased risk of heart failure, obstructive sleep apnea, and malignancy. Conclusion: MAFLD can significantly elevate the risk of systemic diseases and mortality. The care of MAFLD thus requires interdisciplinary collaboration, and future clinical trials conducted on MAFLD should aim to reduce the incidence of end-organ damage aside from improving liver histology.
AB - Objective: The recent introduction of the term metabolic associated fatty liver disease (MAFLD) sought to reclassify nonalcoholic fatty liver disease (NAFLD). MAFLD is thought to improve the encapsulation of metabolic dysregulation. However, recent evidence has found significant differences between MAFLD and NAFLD, and prevailing knowledge has largely arisen from studies on NAFLD. Hence, we conducted a meta-analysis and systematic review of the outcomes associated with MAFLD. Methods: MEDLINE and Embase databases were searched for articles relating to outcomes in MAFLD. Analysis was conducted in random effects with hazard ratios (HRs) to account for longitudinal risk assessment of mortality and systemic complications. Results: A total of 554 articles were identified, of which 17 articles were included. MAFLD resulted in an increase in the overall mortality (HR, 1.24; confidence interval [CI], 1.13-1.34), cancer-related mortality (HR, 1.27; CI, 1.01-1.54), and cardiovascular disease mortality (HR, 1.28, 1.03-1.53; P =.04) compared with non-MAFLD. MAFLD also increases the risk of cardiovascular events (HR, 1.49; CI, 1.34-1.64; P <.01), stroke (HR, 1.55; CI, 1.37-1.73; P <.01), and chronic kidney disease (HR, 1.53; CI, 1.38-1.68). The presence of MAFLD was also associated with an increased risk of heart failure, obstructive sleep apnea, and malignancy. Conclusion: MAFLD can significantly elevate the risk of systemic diseases and mortality. The care of MAFLD thus requires interdisciplinary collaboration, and future clinical trials conducted on MAFLD should aim to reduce the incidence of end-organ damage aside from improving liver histology.
KW - MAFLD
KW - NAFLD
KW - cardiovascular disease
KW - chronic kidney disease
KW - outcomes
KW - stroke
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U2 - 10.1016/j.eprac.2022.03.016
DO - 10.1016/j.eprac.2022.03.016
M3 - Article
C2 - 35364328
AN - SCOPUS:85128326043
VL - 28
SP - 667
EP - 672
JO - Endocrine Practice
JF - Endocrine Practice
SN - 1530-891X
IS - 7
ER -