Associations between inflammatory markers, body composition, and physical function: the Copenhagen Sarcopenia Study

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Associations between inflammatory markers, body composition, and physical function : the Copenhagen Sarcopenia Study. / Kamper, Rikke S.; Alcazar, Julian; Andersen, Lars L.; Haddock, Bryan; Jørgensen, Niklas Rye; Hovind, Peter; Suetta, Charlotte.

In: Journal of Cachexia, Sarcopenia and Muscle, Vol. 12, No. 6, 2021, p. 1641-1652.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kamper, RS, Alcazar, J, Andersen, LL, Haddock, B, Jørgensen, NR, Hovind, P & Suetta, C 2021, 'Associations between inflammatory markers, body composition, and physical function: the Copenhagen Sarcopenia Study', Journal of Cachexia, Sarcopenia and Muscle, vol. 12, no. 6, pp. 1641-1652. https://doi.org/10.1002/jcsm.12832

APA

Kamper, R. S., Alcazar, J., Andersen, L. L., Haddock, B., Jørgensen, N. R., Hovind, P., & Suetta, C. (2021). Associations between inflammatory markers, body composition, and physical function: the Copenhagen Sarcopenia Study. Journal of Cachexia, Sarcopenia and Muscle, 12(6), 1641-1652. https://doi.org/10.1002/jcsm.12832

Vancouver

Kamper RS, Alcazar J, Andersen LL, Haddock B, Jørgensen NR, Hovind P et al. Associations between inflammatory markers, body composition, and physical function: the Copenhagen Sarcopenia Study. Journal of Cachexia, Sarcopenia and Muscle. 2021;12(6):1641-1652. https://doi.org/10.1002/jcsm.12832

Author

Kamper, Rikke S. ; Alcazar, Julian ; Andersen, Lars L. ; Haddock, Bryan ; Jørgensen, Niklas Rye ; Hovind, Peter ; Suetta, Charlotte. / Associations between inflammatory markers, body composition, and physical function : the Copenhagen Sarcopenia Study. In: Journal of Cachexia, Sarcopenia and Muscle. 2021 ; Vol. 12, No. 6. pp. 1641-1652.

Bibtex

@article{8fe945ce6d9549e989f150903b12811c,
title = "Associations between inflammatory markers, body composition, and physical function: the Copenhagen Sarcopenia Study",
abstract = "Background: Chronic low-grade inflammation has been suggested as one of the key elements in the development of sarcopenia, but in contrast to disease-related loss of muscle mass, the role of chronic low-grade inflammation in age-related (primary) sarcopenia is still not clear. The aim of this study was to investigate low-grade inflammation in relation to age and the potential association between inflammatory biomarkers and body composition, muscle strength and physical performance in a healthy Danish cohort. Methods: There were 1160 generally healthy men and women (range: 22–93 years) included. Appendicular lean mass (ALM) and visceral fat normalized to height (kg/m2) was assessed by dual-energy X-ray absorptiometry (iDXA, GE Lunar). Muscle strength and physical performance were evaluated by handgrip strength (HGS), 30 s sit-to-stand performance, and maximal gait speed (GS). Systemic levels of TNF-α, IL-6, IL-1β, IL-4, IL-13, and IFN-γ were measured using multiplex bead-based immunoassays (Bio-Rad). hsCRP was assessed using latex particle-enhanced immunoturbidimetric assays (Roche Diagnostics). Results: With age, ALM/h2, HGS, sit-to-stand performance and GS decreased, whereas visceral fat/h2 increased in both men and women (P < 0.05). Systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased with age in men and women (P < 0.05), while IL-1β increased in women only (P < 0.01). Higher levels of hsCRP were associated with lower ALM/h2 in elderly (≥65 years) men and women (P < 0.001). Higher levels of hsCRP were associated with lower handgrip strength in elderly women (P < 0.05) whereas higher levels of hsCRP was not associated with lower HGS in elderly men (P = 0.056). Higher levels of hsCRP were associated with lower GS (P < 0.05), whereas IFN-γ was positively associated with GS in elderly women (P < 0.05), but not elderly men. Visceral fat index was positively associated with hsCRP in elderly men and women (P < 0.001). Compared with elderly with normal HGS, elderly men and women with low HGS displayed higher levels of TNF-α and hsCRP (P < 0.05). Conclusions: With age, systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased, with hsCRP and TNF-α being especially elevated in more physically frail elderly supporting the association between low-grade systemic inflammation and poor physical function. In contrast, only high levels of hsCRP were weakly associated with low muscle mass and positively associated with visceral fat and low physical function, suggesting that chronic low-grade inflammation is not the main driver of age-related loss of muscle mass as previously suggested.",
keywords = "Ageing, Inflammation, Muscle mass, Muscle strength, Physical function",
author = "Kamper, {Rikke S.} and Julian Alcazar and Andersen, {Lars L.} and Bryan Haddock and J{\o}rgensen, {Niklas Rye} and Peter Hovind and Charlotte Suetta",
note = "Publisher Copyright: {\textcopyright} 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.",
year = "2021",
doi = "10.1002/jcsm.12832",
language = "English",
volume = "12",
pages = "1641--1652",
journal = "Journal of Cachexia, Sarcopenia and Muscle",
issn = "2190-5991",
publisher = "Wiley",
number = "6",

}

RIS

TY - JOUR

T1 - Associations between inflammatory markers, body composition, and physical function

T2 - the Copenhagen Sarcopenia Study

AU - Kamper, Rikke S.

AU - Alcazar, Julian

AU - Andersen, Lars L.

AU - Haddock, Bryan

AU - Jørgensen, Niklas Rye

AU - Hovind, Peter

AU - Suetta, Charlotte

N1 - Publisher Copyright: © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

PY - 2021

Y1 - 2021

N2 - Background: Chronic low-grade inflammation has been suggested as one of the key elements in the development of sarcopenia, but in contrast to disease-related loss of muscle mass, the role of chronic low-grade inflammation in age-related (primary) sarcopenia is still not clear. The aim of this study was to investigate low-grade inflammation in relation to age and the potential association between inflammatory biomarkers and body composition, muscle strength and physical performance in a healthy Danish cohort. Methods: There were 1160 generally healthy men and women (range: 22–93 years) included. Appendicular lean mass (ALM) and visceral fat normalized to height (kg/m2) was assessed by dual-energy X-ray absorptiometry (iDXA, GE Lunar). Muscle strength and physical performance were evaluated by handgrip strength (HGS), 30 s sit-to-stand performance, and maximal gait speed (GS). Systemic levels of TNF-α, IL-6, IL-1β, IL-4, IL-13, and IFN-γ were measured using multiplex bead-based immunoassays (Bio-Rad). hsCRP was assessed using latex particle-enhanced immunoturbidimetric assays (Roche Diagnostics). Results: With age, ALM/h2, HGS, sit-to-stand performance and GS decreased, whereas visceral fat/h2 increased in both men and women (P < 0.05). Systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased with age in men and women (P < 0.05), while IL-1β increased in women only (P < 0.01). Higher levels of hsCRP were associated with lower ALM/h2 in elderly (≥65 years) men and women (P < 0.001). Higher levels of hsCRP were associated with lower handgrip strength in elderly women (P < 0.05) whereas higher levels of hsCRP was not associated with lower HGS in elderly men (P = 0.056). Higher levels of hsCRP were associated with lower GS (P < 0.05), whereas IFN-γ was positively associated with GS in elderly women (P < 0.05), but not elderly men. Visceral fat index was positively associated with hsCRP in elderly men and women (P < 0.001). Compared with elderly with normal HGS, elderly men and women with low HGS displayed higher levels of TNF-α and hsCRP (P < 0.05). Conclusions: With age, systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased, with hsCRP and TNF-α being especially elevated in more physically frail elderly supporting the association between low-grade systemic inflammation and poor physical function. In contrast, only high levels of hsCRP were weakly associated with low muscle mass and positively associated with visceral fat and low physical function, suggesting that chronic low-grade inflammation is not the main driver of age-related loss of muscle mass as previously suggested.

AB - Background: Chronic low-grade inflammation has been suggested as one of the key elements in the development of sarcopenia, but in contrast to disease-related loss of muscle mass, the role of chronic low-grade inflammation in age-related (primary) sarcopenia is still not clear. The aim of this study was to investigate low-grade inflammation in relation to age and the potential association between inflammatory biomarkers and body composition, muscle strength and physical performance in a healthy Danish cohort. Methods: There were 1160 generally healthy men and women (range: 22–93 years) included. Appendicular lean mass (ALM) and visceral fat normalized to height (kg/m2) was assessed by dual-energy X-ray absorptiometry (iDXA, GE Lunar). Muscle strength and physical performance were evaluated by handgrip strength (HGS), 30 s sit-to-stand performance, and maximal gait speed (GS). Systemic levels of TNF-α, IL-6, IL-1β, IL-4, IL-13, and IFN-γ were measured using multiplex bead-based immunoassays (Bio-Rad). hsCRP was assessed using latex particle-enhanced immunoturbidimetric assays (Roche Diagnostics). Results: With age, ALM/h2, HGS, sit-to-stand performance and GS decreased, whereas visceral fat/h2 increased in both men and women (P < 0.05). Systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased with age in men and women (P < 0.05), while IL-1β increased in women only (P < 0.01). Higher levels of hsCRP were associated with lower ALM/h2 in elderly (≥65 years) men and women (P < 0.001). Higher levels of hsCRP were associated with lower handgrip strength in elderly women (P < 0.05) whereas higher levels of hsCRP was not associated with lower HGS in elderly men (P = 0.056). Higher levels of hsCRP were associated with lower GS (P < 0.05), whereas IFN-γ was positively associated with GS in elderly women (P < 0.05), but not elderly men. Visceral fat index was positively associated with hsCRP in elderly men and women (P < 0.001). Compared with elderly with normal HGS, elderly men and women with low HGS displayed higher levels of TNF-α and hsCRP (P < 0.05). Conclusions: With age, systemic levels of hsCRP, TNF-α, IL-4, and IFN-γ increased, with hsCRP and TNF-α being especially elevated in more physically frail elderly supporting the association between low-grade systemic inflammation and poor physical function. In contrast, only high levels of hsCRP were weakly associated with low muscle mass and positively associated with visceral fat and low physical function, suggesting that chronic low-grade inflammation is not the main driver of age-related loss of muscle mass as previously suggested.

KW - Ageing

KW - Inflammation

KW - Muscle mass

KW - Muscle strength

KW - Physical function

U2 - 10.1002/jcsm.12832

DO - 10.1002/jcsm.12832

M3 - Journal article

C2 - 34708570

AN - SCOPUS:85118224819

VL - 12

SP - 1641

EP - 1652

JO - Journal of Cachexia, Sarcopenia and Muscle

JF - Journal of Cachexia, Sarcopenia and Muscle

SN - 2190-5991

IS - 6

ER -

ID: 284110135