Abstract

Objective: The aim of this study was to assess the relationship between basal metabolic rate (BMR) and all-cause mortality in southern Chinese adults.Methods: We prospectively examined the relationship between BMR and all-cause mortality in 12,608 Southern Chinese adults with age ≥ 35 years who participated in the National Key R&D Program from 2013–2014 to 2019–2020. Cox proportional hazard models were used to examine the association between BMR and all-cause mortality.Results: A total of 809 deaths (including 478 men and 331 women) occurred during a median follow-up period of 5.60 years. All-cause mortality was higher in elderly individuals than in non-elderly individuals (11.48 vs. 2.04%, P < 0.001) and was higher in male subjects than in female subjects (9.84 vs. 4.56%, P < 0.001). There was a significantly inverse relationship between BMR levels and all-cause mortality in elderly male individuals (adjusted-HR per SD increase: 0.80, 95% CI: 0.70–0.91, P < 0.001). Compared with BMR levels ≤ 1,115 kJ/day, there was lower all-cause mortality in third and highest BMR quartiles in the elderly male subjects (adjusted-HR: 0.71, 95% CI: 0.53–0.95, P = 0.022; adjusted-HR: 0.60, 95% CI: 0.43–0.84, P = 0.003, respectively).Conclusion: An elevated BMR was independently inversely associated with all-cause mortality in elderly male subjects in a southern Chinese population.

Highlights

  • The question of why we age and die has been a central subject in the life, medical, and health sciences

  • We prospectively examined the relationship between basal metabolic rate (BMR) and all-cause mortality in 12,608 Southern Chinese adults with age ≥ 35 years who participated in the National Key R&D Program from 2013–2014 to 2019–2020

  • There was a significantly inverse relationship between BMR levels and all-cause mortality in elderly male individuals

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Summary

Introduction

The question of why we age and die has been a central subject in the life, medical, and health sciences. At the beginning of the twentieth century, scientists noticed that larger, longer-lived animals had lower basal metabolic rate (BMR), and that the product of their metabolism (per gram) and lifespan was essentially constant (Rubner, 1908). These data formed a cornerstone of the rate-ofliving hypothesis (Lints, 1989) and the free radical damage theory (Beckman and Ames, 1998) of aging, both of which put forward that the longevity of different animal species is inversely proportional to their energy expenditure. Production of damaging reactive oxygen species from metabolism is thought to cause greater oxidative stress and decreased longevity (Lints, 1989; Beckman and Ames, 1998; Brys et al, 2007; Monaghan et al, 2009).

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