MAFLD might be better in identifying subjects with sarcopenia or cardiovascular risk than NAFLD: A nationwide study

Eugene Han1, Ho Soo Chun2,3, Yong-Ho Lee3,4

  • 1Department of Internal Medicine, Keimyung University School of Medicine, Daegu, South Korea.

Abstract

Insights

Metabolic dysfunction-associated fatty liver disease (MAFLD) poses higher risks for sarcopenia and cardiovascular disease (CVD) compared to non-metabolic risk non-alcoholic fatty liver disease (NAFLD). MAFLD criteria may better identify high-risk fatty liver patients.

Area of Science:

  • Hepatology
  • Metabolic Syndrome
  • Cardiovascular Health

Background:

  • Non-alcoholic fatty liver disease (NAFLD) clinical features without metabolic dysfunction criteria are not well understood.
  • Metabolic dysfunction-associated fatty liver disease (MAFLD) is a distinct entity requiring further investigation.
  • The comparative risks of sarcopenia and cardiovascular disease (CVD) between MAFLD and non-metabolic risk NAFLD are unclear.

Purpose of the Study:

  • To investigate the risks of sarcopenia and CVD in patients with MAFLD versus those with NAFLD but without metabolic dysfunction (non-MR NAFLD).
  • To compare the diagnostic utility of MAFLD criteria versus NAFLD criteria in identifying high-risk individuals.

Main Methods:

  • Utilized data from the Korean National Health and Nutrition Examination Surveys (2008-2011).
  • Assessed liver steatosis using the fatty liver index and significant liver fibrosis using the fibrosis-4 index.
  • Defined sarcopenia based on the lowest quintile of the sarcopenia index and high atherosclerotic CVD (ASCVD) risk as a score >10%.

Main Results:

  • The MAFLD group exhibited significantly higher risks of sarcopenia (aOR=3.38) and high ASCVD probability (aOR=3.73) compared to the non-MR NAFLD group.
  • In the non-MR NAFLD group, risks of sarcopenia and high ASCVD probability did not differ based on the presence of significant fibrosis.
  • The MAFLD/non-NAFLD group also showed significantly higher risks of sarcopenia (aOR=2.71) and high ASCVD probability (aOR=2.79) compared to the non-MR NAFLD group.

Conclusions:

  • MAFLD is associated with significantly elevated risks of sarcopenia and CVD.
  • Fibrotic burden did not influence these risks within the non-MR NAFLD group.
  • The MAFLD classification appears more effective than NAFLD criteria for identifying individuals at higher risk of sarcopenia and CVD.

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