Physical activity attenuates the excess mortality risk from prolonged sitting time among adults with osteoporosis or osteopenia.

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrine Pub Date : 2024-09-01 Epub Date: 2024-05-17 DOI:10.1007/s12020-024-03871-8
Zhuoshuai Liang, Jia Lan, Xiaoyue Sun, Ruifang Guo, Yuyang Tian, Yujian Wang, Yawen Liu, Siyu Liu
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Abstract

Purpose: Osteoporosis is a common generalized skeletal disorder characterized by compromised bone strength predisposing a person to an increased risk of fracture. This study aims to crystallize associations of physical activity (PA) and sedentary behaviour with the survival of adults with osteoporosis or osteopenia.

Methods: A total of 3103 participants aged 50 years or older from the National Health and Nutrition Examination Survey (NHANES) were included in the study. All participants were diagnosed with osteopenia or osteoporosis. Multivariable Cox proportional hazards regression models were used to assess the association of PA and sedentary behaviour with overall mortality, cancer-related mortality, and cardiovascular disease (CVD)-related mortality.

Results: During 21349 person-years of follow-up, 675 deaths were documented. Highly active participants had a lower risk of all-cause (hazard ratios [HR] = 0.61; 95% confidence interval [CI], 0.42-0.87; P for trend = 0.004), cancer-specific (HR = 0.64; 95%CI, 0.35-1.17; P for trend = 0.132), CVD-specific (HR = 0.75; 95%CI, 0.45-1.25; P for trend = 0.452), and other (HR, 0.51; 95%CI, 0.29-0.88; P for trend = 0.005) mortality than inactive participants. And sitting time was not associated with mortality among physically active participants; while among those who were insufficiently active or inactive, longer sitting time was associated with increased risks of all-cause (HR per 1-h increase = 1.05; 95% CI, 1.01-1.09), cancer-specific (HR per 1 h increase = 0.98; 95% CI, 0.90-1.07), CVD-specific (HR per 1-h increase = 1.11; 95% CI = 1.04-1.18), and other (HR per 1-h increase = 1.05; 95% CI, 0.98-1.13) mortality in a dose-response manner.

Conclusions: PA can attenuate the excess mortality risk from prolonged sitting for individuals with osteoporosis and/or osteopenia. The combination of prolonged sedentary behaviour with inactive (participants without any PA during a week) PA was associated with an increased risk of mortality. The all-cause mortality risk of individuals who engage in less than 150 min/wk PA and sit more than 8 h/d is 2.02 (95% CI, 1.37-2.99) times higher than that of individuals who engage in more than 150 min/wk PA and sit less than 4 h/d.

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在患有骨质疏松症或骨质增生的成年人中,体育锻炼可降低因久坐而导致的超额死亡风险。
目的:骨质疏松症是一种常见的全身性骨骼疾病,其特点是骨强度受损,容易增加骨折风险。本研究旨在明确体力活动(PA)和久坐行为与骨质疏松症或骨质疏松症成人生存的关系:研究共纳入了 3103 名来自美国国家健康与营养调查(NHANES)的 50 岁或以上的参与者。所有参与者均被诊断为骨质疏松或骨质增生。研究采用多变量考克斯比例危险回归模型来评估活动量和久坐行为与总死亡率、癌症相关死亡率和心血管疾病(CVD)相关死亡率的关系:在 21349 人年的跟踪调查中,有 675 例死亡记录。高度活跃的参与者的全因(危险比 [HR] = 0.61;95% 置信区间 [CI],0.42-0.87;趋势 P = 0.004)、癌症特异性(HR = 0.64;95%CI,0.35-1.17; P for trend = 0.132)、心血管疾病特异性(HR = 0.75; 95%CI, 0.45-1.25; P for trend = 0.452)和其他(HR, 0.51; 95%CI, 0.29-0.88; P for trend = 0.005)死亡率。久坐时间与体力活动参与者的死亡率无关;而在体力活动不足或不活动的参与者中,久坐时间越长,全因死亡率(每增加 1 小时的 HR = 1.05;95% CI,1.01-1.09)、癌症特异性死亡率(每增加 1 小时的 HR = 0.98;95% CI,0.90-1.07)、心血管疾病特异性死亡率(每增加 1 小时的 HR = 1.11;95% CI = 1.04-1.18)和其他死亡率(每增加 1 小时的 HR = 1.05;95% CI,0.98-1.13)的增加与剂量反应相关:结论:对于患有骨质疏松症和/或骨质增生的人来说,久坐可降低因久坐而导致的超额死亡风险。长期久坐行为与不活跃(参与者一周内未进行任何活动)活动相结合,会增加死亡风险。每周参与活动时间少于 150 分钟且每天坐超过 8 小时的人的全因死亡风险是每周参与活动时间超过 150 分钟且每天坐少于 4 小时的人的 2.02 倍(95% CI,1.37-2.99)。
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来源期刊
Endocrine
Endocrine ENDOCRINOLOGY & METABOLISM-
CiteScore
6.50
自引率
5.40%
发文量
295
审稿时长
1.5 months
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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