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Muscle Mass and Inflammation in Older Adults: Impact of the Metabolic Syndrome. | LitMetric

Muscle Mass and Inflammation in Older Adults: Impact of the Metabolic Syndrome.

Gerontology

Department of Endocrinology and Metabolic Diseases (including Division of Lipid Metabolism), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.

Published: September 2022

AI Article Synopsis

  • Inflammation contributes to muscle loss, particularly in individuals with metabolic syndrome (MetS), which is a common age-related condition.
  • A study involving 1,377 participants found that high levels of inflammatory markers, particularly C-reactive protein (CRP) and interleukin-6 (IL-6), were linked to lower muscle mass, while other markers like TNF and IL-10 showed no significant association.
  • The findings suggest that managing MetS could help mitigate inflammation-related muscle loss, indicating the need for intervention studies to explore effective strategies.

Article Abstract

Background: Inflammatory processes are a cause of accelerated loss of muscle mass. Metabolic syndrome (MetS) is a highly prevalent age-related condition, which may promote and be promoted by inflammation. However, whether inflammation in MetS (metaflammation) is associated with lower muscle mass is still unclear.

Methods: Complete cross-sectional data on body composition, MetS, and the inflammatory markers interleukin (IL)-1β, IL-6, IL-10, tumor necrosis factor (TNF), and C-reactive protein (CRP) were available for 1,377 BASE-II participants (51.1% women; 68 ± 4 years old). Appendicular lean mass (ALM) was assessed by dual-energy X-ray absorptiometry. Low muscle mass (low ALM-to-BMI ratio [ALMBMI]) was defined according to the Foundation for the National Institutes of Health (FNIH) Sarcopenia Project. Regression models, adjusted for an increasing number of confounders (sex, age, physical activity, morbidities, diabetes mellitus type II, TSH, albumin, HbA1c, smoking habits, alcohol intake, education, and energy intake/day), were used to calculate the association between low ALMBMI and high inflammation (tertile 3) according to MetS.

Results: MetS was present in 36.2% of the study population, and 9% had low ALMBMI. In the whole study population, high CRP (odds ratio [OR]: 2.7 [95% CI: 1.6-4.7; p = 0.001]) and high IL-6 (OR: 2.1 [95% CI: 1.2-1.9; p = 0.005]) were associated with low ALMBMI. In contrast, no significant association was found between TNF, IL-10, or IL-1β with low ALMBMI. When participants were stratified by MetS, results for IL-6 remained significant only in participants with MetS.

Conclusions: Among BASE-II participants, low ALMBMI was associated with inflammation. Low-grade inflammation triggered by disease state, especially in the context of MetS, might favor loss of muscle mass, so a better control of MetS might help to prevent sarcopenia. Intervention studies to test whether strategies to prevent MetS might also prevent loss of muscle mass seem to be promising.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501741PMC
http://dx.doi.org/10.1159/000520096DOI Listing

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