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RESEARCH PAPER / 2025-01-09

MicroRNA signatures of VO2peak in older adult participants of the Study of Muscle, Mobility and Aging

Karere, G., Hsu, F.-C., Hepple, R. T., Coen, P. M., Cummings, S., Newman, A., Glynn, N. W., Sparks, L., Lane, N. E., Xu, J., Wagner, N., Li, G., Chan, J., Cox, L. A., Kritchevsky, S.

Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USADepartment of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA · biorxiv

Abstract

Background: Peak oxygen consumption during exercise (VO2peak), is a direct measure of cardiorespiratory fitness (CF), a key indicator of physical function and overall health. However, the molecular changes that underpin VO2peak variation are not clear. Our objective is to understand the miRNA signatures that relate to VO2peak variation, which could provide insights to novel mechanisms that contribute to low VO2peak. Methods: We used small RNA sequencing to analyze serum samples from 72 participants (70-79 yrs old, 53% female) of the Study of Muscle, Mobility and Aging (SOMMA). We analyzed samples from individuals with low or high VO2peak (N=18/group) as well as samples from 36 randomly selected participants spanning the entire spectrum of VO2peak. We used LIMMA analysis package for regression analysis and to identify differentially expressed miRNAs. We used receiver operating characteristic curve analysis to evaluate the Area Under the Curve (AUC) and sensitivity and specificity rates. Results: We identified 1,055 miRNAs expressed in all serum samples. Expression of 65 miRNAs differed between participants with low and high VO2peak (p < 0.05). After p-value adjustment, expression of 5 miRNAs (miR-1301-3p, -431-5p, -501-5p, -519a-3p, and -18a-3p) remained significantly different (FDR = 0.05). The five miRNAs had AUC ranging from 0.77 to 0.84. The optimal sensitivity and specificity ranged from 70 to 80% and 80 to 90%, respectively. After adjustment for age and sex covariates, 46 miRNAs significantly correlated with VO2peak (p < 0.05) and miR-519a-3p remained significant based on adjusted of p-values. Conclusions: We identified a miRNA signature of VO2peak in older individuals that might provide insights to novel mechanisms that drive low VO2peak. Future studies will validate the findings in a larger, longitudinal study cohort.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper investigates the molecular signatures associated with VO2peak in older adults, which is relevant to understanding physical function and overall health in the context of aging. However, while it identifies potential biomarkers, the findings are preliminary and require further validation in larger studies. The contribution is solid but does not significantly advance the field of longevity research or address root causes of aging, thus limiting its impact.

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