TY - JOUR
T1 - Type 2 Diabetes Mellitus Is a Risk Factor for Skeletal Muscle Loss in the Course of Dietary Treatment for Patients with Metabolic Dysfunction-associated Steatotic Liver Disease
AU - Sano, Akitoshi
AU - Sasaki, Manami
AU - Inoue, Jun
AU - Kakazu, Eiji
AU - Ninomiya, Masashi
AU - Tsuruoka, Mio
AU - Sato, Kosuke
AU - Onuki, Masazumi
AU - Sawahashi, Satoko
AU - Ouchi, Keishi
AU - Doi, Kotaro
AU - Katori, Yukio
AU - Masamune, Atsushi
N1 - Publisher Copyright:
© 2025 The Japanese Society of Internal Medicine.
PY - 2025
Y1 - 2025
N2 - Objective This study assessed the impact of dietary therapy and reduced body weight on the loss of skeletal muscle in patients with metabolic dysfunction-associated steatotic liver disease (MASLD). Methods This was a single-center retrospective observational study. We enrolled 129 patients with MASLD who had undergone dietary therapy at our facility. We assessed skeletal muscle mass using a bioelectrical impedance analysis at the start of dietary treatment and 12 months after the first assessment. Variables related to muscle reduction were analyzed using a logistic regression model. Results One hundred and eighteen cases were analyzed, excluding those with missing data. In the muscle reduction group, there were more subjects with body weight reduction than in the control group (68% and 40%, respectively, p=0.002), and their body mass index (BMI) was decreased (-0.7 kg/m2 and +0.3 kg/m2, respectively, p=0.0003). There was a significant correlation between the changes in the BMI and muscle mass (R=0.48, p<0.0001). We standardized muscle mass change by dividing it by weight change to analyze the severe decrease in muscle mass compared to weight change. A logistic regression analysis revealed that type 2 diabetes mellitus (T2DM) was an independent variable related to severe skeletal muscle loss (odds ratio, 2.69; 95% CI: 1.13-6.42, p=0.03). Conclusion Weight loss is associated with skeletal muscle loss during dietary treatment for MASLD. T2 DM is a risk factor for severe skeletal muscle loss.
AB - Objective This study assessed the impact of dietary therapy and reduced body weight on the loss of skeletal muscle in patients with metabolic dysfunction-associated steatotic liver disease (MASLD). Methods This was a single-center retrospective observational study. We enrolled 129 patients with MASLD who had undergone dietary therapy at our facility. We assessed skeletal muscle mass using a bioelectrical impedance analysis at the start of dietary treatment and 12 months after the first assessment. Variables related to muscle reduction were analyzed using a logistic regression model. Results One hundred and eighteen cases were analyzed, excluding those with missing data. In the muscle reduction group, there were more subjects with body weight reduction than in the control group (68% and 40%, respectively, p=0.002), and their body mass index (BMI) was decreased (-0.7 kg/m2 and +0.3 kg/m2, respectively, p=0.0003). There was a significant correlation between the changes in the BMI and muscle mass (R=0.48, p<0.0001). We standardized muscle mass change by dividing it by weight change to analyze the severe decrease in muscle mass compared to weight change. A logistic regression analysis revealed that type 2 diabetes mellitus (T2DM) was an independent variable related to severe skeletal muscle loss (odds ratio, 2.69; 95% CI: 1.13-6.42, p=0.03). Conclusion Weight loss is associated with skeletal muscle loss during dietary treatment for MASLD. T2 DM is a risk factor for severe skeletal muscle loss.
KW - metabolic dysfunction-associated steatotic liver disease
KW - non-alcoholic fatty liver disease
KW - sarcopenia
KW - type 2 diabetes mellitus
UR - http://www.scopus.com/inward/record.url?scp=85219248659&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85219248659&partnerID=8YFLogxK
U2 - 10.2169/internalmedicine.3787-24
DO - 10.2169/internalmedicine.3787-24
M3 - Article
C2 - 39048367
AN - SCOPUS:85219248659
SN - 0918-2918
VL - 64
SP - 631
EP - 641
JO - Internal Medicine
JF - Internal Medicine
IS - 5
ER -