TY - JOUR
T1 - Brain Age Gap Associations with Body Composition and Metabolic Indices in an Asian Cohort
T2 - An MRI-Based Study
AU - Lee, Han Jui
AU - Kuo, Chen Yuan
AU - Tsao, Yu Chung
AU - Lee, Pei Lin
AU - Chou, Kun Hsien
AU - Lin, Chung Jung
AU - Lin, Ching Po
N1 - Publisher Copyright:
© 2025
PY - 2025/6
Y1 - 2025/6
N2 - Background: Global aging raises concerns about cognitive health, metabolic disorders, and sarcopenia. Prevention of reversible decline and diseases in middle-aged individuals is essential for promoting healthy aging. We hypothesize that changes in body composition, specifically muscle mass and visceral fat, and metabolic indices are associated with accelerated brain aging. To explore these relationships, we employed a brain age model to investigate the links between the brain age gap (BAG), body composition, and metabolic markers. Methods: Using T1-weighted anatomical brain MRIs, we developed a machine learning model to predict brain age from gray matter features, trained on 2,675 healthy individuals aged 18–92 years. This model was then applied to a separate cohort of 458 Taiwanese adults (57.8 years ± 11.6; 280 men) to assess associations between BAG, body composition quantified by MRI, and metabolic markers. Results: Our model demonstrated reliable generalizability for predicting individual age in the clinical dataset (MAE = 6.11 years, r = 0.900). Key findings included significant correlations between larger BAG and reduced total abdominal muscle area (r = -0.146, p = 0.018), lower BMI-adjusted skeletal muscle indices, (r = -0.134, p = 0.030), increased systemic inflammation, as indicated by high-sensitivity C-reactive protein levels (r = 0.121, p = 0.048), and elevated fasting glucose levels (r = 0.149, p = 0.020). Conclusions: Our findings confirm that muscle mass and metabolic health decline are associated with accelerated brain aging. Interventions to improve muscle health and metabolic control may mitigate adverse effects of brain aging, supporting healthier aging trajectories.
AB - Background: Global aging raises concerns about cognitive health, metabolic disorders, and sarcopenia. Prevention of reversible decline and diseases in middle-aged individuals is essential for promoting healthy aging. We hypothesize that changes in body composition, specifically muscle mass and visceral fat, and metabolic indices are associated with accelerated brain aging. To explore these relationships, we employed a brain age model to investigate the links between the brain age gap (BAG), body composition, and metabolic markers. Methods: Using T1-weighted anatomical brain MRIs, we developed a machine learning model to predict brain age from gray matter features, trained on 2,675 healthy individuals aged 18–92 years. This model was then applied to a separate cohort of 458 Taiwanese adults (57.8 years ± 11.6; 280 men) to assess associations between BAG, body composition quantified by MRI, and metabolic markers. Results: Our model demonstrated reliable generalizability for predicting individual age in the clinical dataset (MAE = 6.11 years, r = 0.900). Key findings included significant correlations between larger BAG and reduced total abdominal muscle area (r = -0.146, p = 0.018), lower BMI-adjusted skeletal muscle indices, (r = -0.134, p = 0.030), increased systemic inflammation, as indicated by high-sensitivity C-reactive protein levels (r = 0.121, p = 0.048), and elevated fasting glucose levels (r = 0.149, p = 0.020). Conclusions: Our findings confirm that muscle mass and metabolic health decline are associated with accelerated brain aging. Interventions to improve muscle health and metabolic control may mitigate adverse effects of brain aging, supporting healthier aging trajectories.
KW - Aging
KW - Body composition
KW - Brain age
KW - MRI
KW - Muscle mass
KW - Sarcopenia
UR - https://www.scopus.com/pages/publications/105000532281
U2 - 10.1016/j.archger.2025.105830
DO - 10.1016/j.archger.2025.105830
M3 - Article
C2 - 40127523
AN - SCOPUS:105000532281
SN - 0167-4943
VL - 133
JO - Archives of Gerontology and Geriatrics
JF - Archives of Gerontology and Geriatrics
M1 - 105830
ER -