Muscle-derived microRNAs correlated with thigh lean mass gains during progressive resistance training in older adults.
Samia M O'Bryan, Kaleen M Lavin, Zachary A Graham, Devin J Drummer, S Craig Tuggle, Kendall Van Keuren-Jensen, Rebecca Reiman, Eric Alsop, Madhavi P Kadakia, Michael P Craig, Jin Zhang, Marcas M Bamman
Author Information
Samia M O'Bryan: UAB Center for Exercise Medicine, The University of Alabama at Birmingham, Birmingham, Alabama, United States. ORCID
Kaleen M Lavin: Healthspan, Resilience, and Performance Research, Florida Institute for Human and Machine Cognition, Pensacola, Florida, United States. ORCID
Zachary A Graham: Healthspan, Resilience, and Performance Research, Florida Institute for Human and Machine Cognition, Pensacola, Florida, United States.
Devin J Drummer: UAB Center for Exercise Medicine, The University of Alabama at Birmingham, Birmingham, Alabama, United States. ORCID
S Craig Tuggle: Healthspan, Resilience, and Performance Research, Florida Institute for Human and Machine Cognition, Pensacola, Florida, United States.
Kendall Van Keuren-Jensen: Translational Genomics Research Institute, Phoenix, Arizona, United States.
Rebecca Reiman: Translational Genomics Research Institute, Phoenix, Arizona, United States.
Eric Alsop: Translational Genomics Research Institute, Phoenix, Arizona, United States.
Madhavi P Kadakia: Boonshoft School of Medicine, Wright State University, Dayton, Ohio, United States.
Michael P Craig: Boonshoft School of Medicine, Wright State University, Dayton, Ohio, United States.
Jin Zhang: Boonshoft School of Medicine, Wright State University, Dayton, Ohio, United States.
Marcas M Bamman: UAB Center for Exercise Medicine, The University of Alabama at Birmingham, Birmingham, Alabama, United States. ORCID
Resistance training (RT) remains the most effective treatment for age-related declines in muscle mass. However, many older adults experience attenuated muscle hypertrophy in response to RT when compared with younger adults. This may be attributed to underlying molecular processes that are dysregulated by aging and exacerbated by improperly prescribed RT weekly volume, intensity, and/or frequency doses. MicroRNAs (miRNAs) are key epigenetic regulators that impact signaling pathways and protein expression within cells, are dynamic and responsive to exercise stimuli, and are often dysregulated in diseases. In this study, we used untargeted miRNA-seq to examine miRNA in skeletal muscle and serum-derived exosomes of older adults ( = 18, 11 M/7 F, 66 �� 1 yr) who underwent three times per wk RT for 30 wk [e.g., high intensity three times/wk (HHH, = 9) or alternating high-low-high (HLH) intensity ( = 9)], after a standardized 4-wk washin. Within each tissue, miRNAs were clustered into modules based on pairwise correlation using weighted gene correlation network analysis (WGCNA). Modules were tested for association with the magnitude of RT-induced thigh lean mass (TLM) change [as measured by dual-energy X-ray absorptiometry (DXA)]. Although no modules were unique to training dose, we identified miRNA modules in skeletal muscle associated with TLM gains irrespective of exercise dose. Using miRNA-target interactions, we analyzed key miRNAs in significant modules for their potential regulatory involvement in biological pathways. Findings point toward potential miRNAs that may be informative biomarkers and could also be evaluated as potential therapeutic targets as an adjuvant to RT to maximize skeletal muscle mass accrual in older adults. In this work, we identified a set of microRNAs correlated with thigh lean mass gains in a group of older adults. To our knowledge, this is the first time these microRNAs have been identified as novel predictive biomarkers correlating with lean mass gains in aging adults. As biomarkers, these may help interventionalists identify older individuals that are positively responding to an exercise intervention.
