Published online Jun 27, 2025. doi: 10.4254/wjh.v17.i6.107931
Revised: April 22, 2025
Accepted: June 4, 2025
Published online: June 27, 2025
Processing time: 86 Days and 19.9 Hours
Improving our understanding of whether increased dietary intake of ω-3 polyunsaturated fatty acids (PUFAs) is beneficial for increasing skeletal muscle mass in patients with metabolic dysfunction-associated fatty liver disease (MAFLD) could provide an important clinical evidence base for the development of relevant nutritional guidelines.
To investigate the effect of total dietary ω-3 PUFAs and their subtypes on skeletal muscle mass in MAFLD.
This cross-sectional study involved 2316 participants from four National Health and Nutrition Examination Survey cycles between 2011 and 2018. Dietary intake of ω-3 PUFAs was collected through 24-hour dietary recall interviews. Appen
The multiple linear regression model showed significant relationships for dietary intake of total ω-3 PUFAs with higher ASMI (β: 0.06, 95%CI: 0.01–0.11) in MAFLD patients. Dietary a-linolenic acid (ALA) (β: 0.06, 95%CI: 0.01–0.12), docosapentaenoic acid (β: 1.28, 95%CI: 0.01–2.54), and docosahexaenoic acid (DHA) (β: 0.19, 95%CI: 0.01–0.37) were significantly associated with higher ASMI, while intake of stearidonic acid and eicosapentaenoic acid did not improve ASMI. In patients with high probability of liver fibrosis, dietary intake of ALA was associated with higher ASMI (β: 0.11, 95%CI: 0.03–0.18). Stratified analysis found that DHA was associated with higher ASMI in patients with obesity and higher metabolic risk.
Increasing dietary intake of ω-3 PUFAs improved skeletal muscle health in patients with MAFLD. Patient with obesity and higher metabolic risk were more likely to benefit from intake of DHA.
Core Tip: This study found that dietary intake of ω-3 polyunsaturated fatty acids improved skeletal muscle mass in patients with metabolic dysfunction-associated fatty liver disease, and patients with obesity and higher metabolic risk were more likely to benefit from supplementation with docosahexaenoic acid. These results fill a gap in muscle nutrient metabolism in patients with fatty liver disease.
