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

  • ,
  • Rodrigo M. Carrillo-Larco
    ,
  • Robert H. Gilman
    ,
  • Liam Smeeth
    ,
  • William Checkley
    ,
  • J. Jaime Miranda
  • ,
  • Universidad Peruana Cayetano Heredia
    ,
  • Imperial College London
    ,
  • Johns Hopkins University
    ,
  • London School of Hygiene and Tropical Medicine
    ,
  • Johns Hopkins University School of Medicine
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 107-115 (9 pages)

Journal (Volume, Issue Number)

Tropical Medicine and International Health (Volume 28, Issue 2)

Publication milestones

  • Accepted/In press - 2022
  • Published - 02/2023

Publication status

Published - 02/2023

ISSN

1360-2276

Publication IDs

  • Scopus: 85145365897
  • PubMed: 36573344

Abstract

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 ρ 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.

Funding Details

The CRONICAS Cohort Study was supported by the National Heart, Lung and Blood Institute Global Health Initiative under the contract Global Health Activities in Developing Countries to Combat Non‐Communicable Chronic Diseases (Project Number 268200900033C‐1‐0‐1). Rodrigo M. Carrillo‐Larco is supported by a Wellcome Trust International Training Fellowship (214185/Z/18/Z). National Heart, Lung and Blood Institute Global Health Initiative, Grant/Award Number: 268200900033C‐1‐0‐1; Wellcome Trust International Training Fellowship, Grant/Award Number: 214185/Z/18/Z Funding information
FundersFunding numbers
NHLBI
268200900033C‐1‐0‐1
WT
214185/Z/18, 214185/Z/18/Z

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