Association of cardiorespiratory fitness with phenotypic age in younger population: a study based on the NHANES database

TL;DR

This study finds that poor cardiorespiratory fitness is linked to faster biological aging in younger people, with obesity worsening the effect.

Contribution

The study provides novel evidence linking cardiorespiratory fitness to phenotypic age acceleration in younger populations.

Findings

High cardiorespiratory fitness is associated with a 42% reduced risk of phenotypic age acceleration.

Impaired cardiorespiratory fitness is linked to a 1.46-year increase in phenotypic age.

Obesity interacts with poor fitness to worsen biological aging in those over 29 years old.

Abstract

Phenotypic age (PA), a novel signature of morbidity and mortality risk based on clinically collected parameters, is considered one of the most promising biomarkers for capturing aging. However, unequivocal evidence on the link between cardiorespiratory fitness (CRF), assessed by estimated maximal oxygen consumption (Vo2max), and PA remains scarce, particularly within the first half of life. This study aims to explore the relationships between CRF and the age-adjusted value derived from the residuals of the regression of PA on chronological age (PhenoageAcceleration: PAA), uncovering the prognostic value of CRF in the early lifetime to provide perspectives for understanding and improving healthy aging.

Data from 3,069 participants in the National Health and Nutrition Examination Survey (NHANES) were included and further examined. CRF status was determined by Vo2max according to gender and age-specific criteria, with low and moderate levels classified as impaired CRF. PA was calculated from multisystem blood biomarkers and chronological age. The association of CRF status with cross-sectional PAA was investigated, and subgroup analyses were further performed to explore and identify potentially vulnerable populations.

In the multivariable logistical regression analysis, maintenance of CRF was significantly and inversely associated with PAA, demonstrating a decreased risk of 42% in the high CRF group [OR (95% CI): 0.58 (0.36, 0.96), p = 0.033]. Compared with those with non-impaired CRF, those in the impaired group exhibited a rise in PA by 1.46 years [β (95% CI): 1.46 (1.03, 2.10), p = 0.040]. Interestingly, in the population of over 29 years’ old, a significant interaction between obesity and impaired CRF for PAA was observed (p = 0.018; p = 0.026).

Poor CRF may serve as a potential risk factor for accelerated biological aging (BA) in relatively young populations, and the existence of obesity could exacerbate the aging process. This represents a potential intervention target for promoting healthy aging across different age groups in the future.

Figures