4.3 Article

Skeletal muscle mass and all-cause mortality: Findings from the CRONICAS cohort study

Journal

TROPICAL MEDICINE & INTERNATIONAL HEALTH
Volume 28, Issue 2, Pages 107-115

Publisher

WILEY
DOI: 10.1111/tmi.13844

Keywords

all-cause mortality; bio-impedance analysis; cohort study; skeletal muscle mass

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The study evaluated the agreement between the equation and bio-impedance analysis methods in estimating skeletal muscle mass and assessed the association between skeletal muscle mass and all-cause mortality risk in different geographical sites in Peru. The study found a strong correlation and agreement between skeletal muscle mass estimates obtained by the equation and bio-impedance analysis. However, an association between skeletal muscle mass and all-cause mortality only exists when using the equation.
Objective: We aimed (1) to evaluate the agreement between two methods (equation and bio-impedance analysis [BIA]) to estimate skeletal muscle mass (SMM), and (2) to assess if SMM was associated with all-cause mortality risk in individuals across different geographical sites in Peru.Methods:We used data from the CRONICAS Cohort Study (2010-2018), a population-based longitudinal study in Peru to assess cardiopulmonary risk factors from different geographical settings. SMM was computed as a function of weight, height, sex and age (Lee equation) and by BIA. All-cause mortality was retrieved from national vital records. Cox proportional-hazard models were developed and results presented as hazard ratios (HRs) with 95% confidence intervals (95% CIs).Results: At baseline, 3216 subjects, 51.5% women, mean age 55.7 years, were analysed. The mean SMM was 23.1 kg (standard deviation [SD]: 6.0) by Lee equation, and 22.7 (SD: 5.6) by BIA. Correlation between SMM estimations was strong (Pearson's rho coefficient = 0.89, p < 0.001); whereas Bland-Altman analysis showed a small mean difference. Mean follow-up was 7.0 (SD: 1.0) years, and there were 172 deaths. In the multivariable model, each additional kg in SMM was associated with a 19% reduction in mortality risk (HR = 0.81; 95% CI: 0.75-0.88) using the Lee equation, but such estimate was not significant when using BIA (HR = 0.98; 95% CI: 0.94-1.03). Compared to the lowest tertile, subjects at the highest SMM tertile had a 56% reduction in risk of mortality using the Lee equation, but there was no such association when using BIA estimations.Conclusion: There is a strong correlation and agreement between SMM estimates obtained by the Lee equation and BIA. However, an association between SMM and all-cause mortality exists only when the Lee equation is used. Our findings call for appropriate use of approaches to estimate SMM, and there should be a focus on muscle mass in promoting healthier ageing.

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