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炎症标志物、身体成分和身体功能之间的关联:哥本哈根肌肉减少症研究。

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

机构信息

Geriatric Research Unit, Department of Geriatric and Palliative Medicine, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen, Denmark.

Department of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet Glostrup, Glostrup, Denmark.

出版信息

J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1641-1652. doi: 10.1002/jcsm.12832. Epub 2021 Oct 27.

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/m ) 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/h , HGS, sit-to-stand performance and GS decreased, whereas visceral fat/h 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/h 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.

摘要

背景

慢性低度炎症被认为是肌肉减少症发展的关键因素之一,但与疾病相关的肌肉质量损失相反,低度炎症在与年龄相关(原发性)肌肉减少症中的作用仍不清楚。本研究旨在探讨低度炎症与年龄的关系,以及炎症生物标志物与身体成分、肌肉力量和身体表现之间的潜在关联,研究对象为丹麦一个健康队列。

方法

纳入了 1160 名一般健康的男性和女性(年龄范围:22-93 岁)。使用双能 X 射线吸收法(iDXA,GE Lunar)评估四肢瘦质量(ALM)和按身高归一化的内脏脂肪(kg/m )。通过握力(HGS)、30 秒坐立起身测试和最大步行速度(GS)评估肌肉力量和身体表现。使用基于多重珠子的免疫分析(Bio-Rad)测量 TNF-α、IL-6、IL-1β、IL-4、IL-13 和 IFN-γ的全身水平。使用乳胶粒子增强免疫比浊测定法(罗氏诊断)评估 hsCRP。

结果

随着年龄的增长,男性和女性的 ALM/h 、HGS、坐立起身表现和 GS 降低,而内脏脂肪/h 增加(P<0.05)。男性和女性的 hsCRP、TNF-α、IL-4 和 IFN-γ水平随年龄增长而升高(P<0.05),而 IL-1β仅在女性中升高(P<0.01)。高龄(≥65 岁)男性和女性的 hsCRP 水平较高与较低的 ALM/h 相关(P<0.001)。高龄女性的 hsCRP 水平较高与较低的握力相关(P<0.05),而高龄男性的 hsCRP 水平与较低的握力无相关性(P=0.056)。hsCRP 水平较高与 GS 较低相关(P<0.05),而 IFN-γ与高龄女性的 GS 呈正相关(P<0.05),但与高龄男性的 GS 无关。内脏脂肪指数与高龄男性和女性的 hsCRP 呈正相关(P<0.001)。与 HGS 正常的高龄男性和女性相比,HGS 较低的高龄男性和女性的 TNF-α和 hsCRP 水平更高(P<0.05)。

结论

随着年龄的增长,hsCRP、TNF-α、IL-4 和 IFN-γ 的全身水平升高,hsCRP 和 TNF-α在身体更虚弱的高龄人群中尤其升高,支持低度全身性炎症与较差的身体功能之间的关联。相比之下,只有 hsCRP 水平较高与低肌肉质量弱相关,与内脏脂肪和低身体功能正相关,这表明慢性低度炎症并不是先前认为的与年龄相关的肌肉质量损失的主要驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2be/8718077/8eb12876d05c/JCSM-12-1641-g001.jpg

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