Physical fitness in community-dwelling older adults is linked to dietary intake, gut microbiota, and metabolomic signatures

• Main Authors: Castro-Mejía, Josué L., Khakimov, Bekzod, Krych, Lukasz, Bülow, Jacob, Bechshøft, Rasmus L., Hojfeldt, Grith, Mertz, Kenneth H., Garne, Eva Stahl, Schacht, Simon R., Hajar Fauzan, Ahmad, Kot, Witold, Hansen, Lars H., Perez-Cueto, Federico J. A., Lind, Mads V., Lassen, Aske J., Tetens, Inge, Jensen, Tenna, Reitelseder, Soren, Jespersen, Astrid P., Holm, Lars, Engelsen, Soren B., Nielsen, Dennis S.
• Format: Article
• Language: English
• Published: John Wiley & Sons Ltd and The Anatomical Society 2020
• Subjects: QR Microbiology; RA0421 Public health. Hygiene. Preventive Medicine; RC1200 Sports Medicine
• Online Access: http://umpir.ump.edu.my/id/eprint/29960/7/Physical%20fitness%20in%20community-dwelling%20older.pdf; http://umpir.ump.edu.my/id/eprint/29960/; https://doi.org/10.1111/acel.13105; https://doi.org/10.1111/acel.13105

When humans age, changes in body composition arise along with lifestyle-associated disorders influencing fitness and physical decline. Here we provide a comprehensive view of dietary intake, physical activity, gut microbiota (GM), and host metabolome in relation to physical fitness of 207 community-dwelling subjects aged +65Â years. Stratification on anthropometric/body composition/physical performance measurements (ABPm) variables identified two phenotypes (high/low-fitness) clearly linked to dietary intake, physical activity, GM, and host metabolome patterns. Strikingly, despite a higher energy intake high-fitness subjects were characterized by leaner bodies and lower fasting proinsulin-C-peptide/blood glucose levels in a mechanism likely driven by higher dietary fiber intake, physical activity and increased abundance of Bifidobacteriales and Clostridiales species in GM and associated metabolites (i.e., enterolactone). These factors explained 50.1% of the individual variation in physical fitness. We propose that targeting dietary strategies for modulation of GM and host metabolome interactions may allow establishing therapeutic approaches to delay and possibly revert comorbidities of aging.