骨密度和肌肉质量在预测全因死亡率中的相互作用:一项针对1388名老年男性(77-101岁)的10年前瞻性队列研究。

IF 6 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Ben Kirk, Stephanie L Harrison, Jesse Zanker, Andrew J Burghardt, Eric Orwoll, Peggy M Cawthon, Gustavo Duque
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引用次数: 0

摘要

背景:低骨密度和低肌肉质量都是老年男性死亡的独立危险因素。然而,尚不清楚这些组织是否相互作用会增加死亡风险。阐明这一信息很重要,因为骨骼和肌肉在整个生命周期中是可以改变的。目的:探讨骨密度和肌肉质量对老年男性全因死亡率的影响。设计:前瞻性队列研究。背景:男性骨质疏松性骨折研究,一项横跨美国6个地点的多中心纵向研究。参与者:基线就诊时(2014-2016年)暴露测量包括通过双能x线骨密度仪(髋关节,g/cm2)测量骨密度;肌酸稀释稳定同位素测定肌肉质量(全身,kg);高分辨率计算机断层扫描显示的骨强度(胫骨,牛顿);高分辨率计算机断层扫描显示肌肉体积(小腿,mm3)。在基线访问(2014-2016年)测量的协变量包括人口统计学和生活方式因素以及医疗条件。主要结局指标:2014年至2016年至2024年8月,通过死亡证明和《国际疾病分类-第九次修订代码》测量的全因死亡率。数据分析于2024年12月进行。Cox风险模型用于模拟暴露与结果之间的关系,未调整和调整协变量。结果:男性1388例,平均年龄84.2±4.1岁(77 ~ 101岁,白人91.6%),随访时间为6.58±2.61年。共有663人(47.8%)死亡。在使用连续暴露的未调整分析中,骨骼和肌肉变量之间的相互作用项对全因死亡率具有显著意义(P结论:我们发现了骨骼和肌肉健康与全因死亡率联合关联的一致证据。现在需要随机对照试验来证实增加或保留老年时的骨骼和肌肉质量是否会降低死亡风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interactions between bone density and muscle mass in predicting all-cause mortality: a 10-year prospective cohort study of 1388 older men (aged 77-101 years).

Background: Low bone density and low muscle mass are both independent risk factors for mortality in older men. However, it is unknown if these tissues interact to increase mortality risk. Elucidating this information is important as bone and muscle are modifiable across the life cycle.

Objective: To examine whether there is an interconnection between bone density and muscle mass on all-cause mortality in older men.

Design: Prospective cohort study.

Setting: The Osteoporotic Fractures in Men study, an multicenter longitudinal study across six US sites.

Participants: Exposures measured at baseline visit (2014-2016) included bone density by dual-energy X-ray absorptiometry (hip, g/cm2); muscle mass by creatine dilution stable isotope (whole body, kg); bone strength by high-resolution computed tomography (tibia, newtons); and muscle volume by high-resolution computed tomography (calf, mm3). Covariates measured at baseline visit (2014-2016) included demographics and lifestyle factors as well as medical conditions.

Main outcome measure: All-cause mortality by death certificates and International Classification of Diseases-Ninth Revision codes measured from 2014 to 2016 through August 2024. Data analysis was performed during December 2024. Cox hazards models were used to model the relationship between the exposures and outcomes, unadjusted and adjusted for covariates.

Results: A total of 1388 men with a mean age of 84.2 ± 4.1 years (77-101 years, 91.6% white) were followed for 6.58 ± 2.61 years. A total of 663 (47.8%) men died. In unadjusted analyses using continuous exposures, interaction terms were significant between bone and muscle variables for all-cause mortality (P < 0.001 to 0.039). In men with low muscle mass or low muscle volume (≤50th percentile), each SD decrease in bone density increased all-cause mortality by a respective 19% (HR = 1.19 95% CI 1.07-1.34) and 29% (HR = 1.29 95% CI 1.11-1.49) in multivariable-adjusted models. Likewise, in men with low muscle mass or low muscle volume (≤50th percentile), each SD decrease in bone strength increased all-cause mortality by a respective 19% (HR = 1.19 95% CI 1.06-1.33) and 29% (HR = 1.29 95% CI 1.12-1.48) in multivariable-adjusted models.

Conclusions: We found consistent evidence for a combined association of bone and muscle health on all-cause mortality. Randomised controlled trials are now needed to confirm if increasing or preserving bone and muscle mass in old age reduces mortality risk.

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来源期刊
Age and ageing
Age and ageing 医学-老年医学
CiteScore
9.20
自引率
6.00%
发文量
796
审稿时长
4-8 weeks
期刊介绍: Age and Ageing is an international journal publishing refereed original articles and commissioned reviews on geriatric medicine and gerontology. Its range includes research on ageing and clinical, epidemiological, and psychological aspects of later life.
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