Chemokine CXCL9, a marker of inflammaging, is associated with changes of muscle strength and mortality in older men.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Osteoporosis International Pub Date : 2024-10-01 Epub Date: 2024-07-04 DOI:10.1007/s00198-024-07160-y
Da Hea Seo, Maripat Corr, Sheena Patel, Li-Yung Lui, Jane A Cauley, Daniel Evans, Theresa Mau, Nancy E Lane
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引用次数: 0

Abstract

Our study examined associations of the CXC motif chemokine ligand 9 (CXCL9), a pro-inflammatory protein implicated in age-related inflammation, with musculoskeletal function in elderly men. We found in certain outcomes both cross-sectional and longitudinal significant associations of CXCL9 with poorer musculoskeletal function and increased mortality in older men. This requires further investigation.

Purpose: We aim to determine the relationship of (CXCL9), a pro-inflammatory protein implicated in age-related inflammation, with both cross-sectional and longitudinal musculoskeletal outcomes and mortality in older men.

Methods: A random sample from the Osteoporotic Fractures in Men (MrOS) Study cohort (N = 300) was chosen for study subjects that had attended the third and fourth clinic visits, and data was available for major musculoskeletal outcomes (6 m walking speed, chair stands), hip bone mineral density (BMD), major osteoporotic fracture, mortality, and serum inflammatory markers. Serum levels of CXCL9 were measured by ELISA, and the associations with musculoskeletal outcomes were assessed by linear regression and fractures and mortality with Cox proportional hazards models.

Results: The mean CXCL9 level of study participants (79.1 ± 5.3 years) was 196.9 ± 135.2 pg/ml. There were significant differences for 6 m walking speed, chair stands, physical activity scores, and history of falls in the past year across the quartiles of CXCL9. However, higher CXCL9 was only significantly associated with changes in chair stands (β =  - 1.098, p < 0.001) even after adjustment for multiple covariates. No significant associations were observed between CXCL9 and major osteoporotic fracture or hip BMD changes. The risk of mortality increased with increasing CXCL9 (hazard ratio quartile (Q)4 vs Q1 1.98, 95% confidence interval 1.25-3.14; p for trend < 0.001).

Conclusions: Greater serum levels of CXCL9 were significantly associated with a decline in chair stands and increased mortality. Additional studies with a larger sample size are needed to confirm our findings.

趋化因子 CXCL9 是一种炎症标志物,它与老年男性肌肉力量的变化和死亡率有关。
我们的研究考察了 CXC motif 趋化因子配体 9(CXCL9)与老年男性肌肉骨骼功能之间的关系,CXCL9 是一种与年龄相关炎症有关联的促炎症蛋白。我们发现,在某些结果中,CXCL9 与肌肉骨骼功能较差和老年男性死亡率升高有显著的横向和纵向关联。目的:我们旨在确定(CXCL9)(一种与年龄相关炎症有牵连的促炎蛋白)与老年男性肌肉骨骼的横向和纵向结果及死亡率之间的关系:从 "男性骨质疏松性骨折(MrOS)研究 "队列(N = 300)中随机抽取第三和第四次门诊就诊的研究对象,并获得主要肌肉骨骼结果(6 米步行速度、椅子站立)、髋部骨矿密度(BMD)、主要骨质疏松性骨折、死亡率和血清炎症标志物的数据。采用酶联免疫吸附法测定血清中的CXCL9水平,通过线性回归评估与肌肉骨骼结果的关系,通过Cox比例危险模型评估骨折和死亡率:研究参与者(79.1 ± 5.3 岁)的平均 CXCL9 水平为 196.9 ± 135.2 pg/ml。不同四分位数的 CXCL9 在 6 米步行速度、椅子站立、体力活动评分和过去一年跌倒史方面存在明显差异。然而,较高的 CXCL9 仅与椅子站立角度的变化有显著相关性(β = - 1.098,p 结论:CXCL9 越高,椅子站立角度越低:血清中 CXCL9 水平升高与椅子站立角度下降和死亡率升高有显著相关性。需要进行更多样本量的研究来证实我们的发现。
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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
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