Associations of sleep behaviors and genetic risk with risk of incident osteoporosis: A prospective cohort study of 293,164 participants

被引:3
作者
Zhao, Hanhan [1 ]
Jia, Hongyu [2 ]
Jiang, Yanfeng [3 ,4 ]
Suo, Chen [1 ,3 ]
Liu, Zhenqiu [3 ,4 ]
Chen, Xingdong [3 ,4 ,5 ,6 ]
Xu, Kelin [1 ,3 ]
机构
[1] Fudan Univ, Sch Publ Hlth, Key Lab Publ Hlth Safety, Minist Educ, Shanghai, Peoples R China
[2] Wuyang Dis Control & Prevent Ctr, Luohe, Henan, Peoples R China
[3] Fudan Univ, Taizhou Inst Hlth Sci, Taizhou, Jiangsu, Peoples R China
[4] Fudan Univ, Human Phenome Inst, Zhangjiang Fudan Int Innovat Ctr, State Key Lab Genet Engn, Shanghai, Peoples R China
[5] Fudan Univ, Huashan Hosp, Natl Clin Res Ctr Aging & Med, Shanghai, Peoples R China
[6] Fudan Univ, Yiwu Res Inst, Yiwu, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Sleep behaviors; Osteoporosis; Genetic risk; Cohort study; DURATION; BONE; HEALTH; APNEA; QUALITY; DISEASE;
D O I
10.1016/j.bone.2024.117168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Unhealthy sleep behaviors are associated with higher risks of osteoporosis (OP), while prospective evidence is limited. This study aimed to prospectively investigate this association, quantify the attributable burden of OP incidence reduction due to unhealthy sleep behaviors, and explore potential modifications by genetic risk factors. Methods: This longitudinal cohort study was conducted utilizing data from the UK Biobank, comprising 293,164 participants initially free of OP and with requisite sleep behaviors data at baseline. We followed the participants after recruitment until November 30, 2022, to ascertain incident OP. We assessed the associations of five sleep behaviors including sleep duration, chronotype, insomnia, daytime napping, and morning wake-up difficulties, as well as sleep behavior patterns identified based on the above sleep behaviors, with the risk of OP, using Cox models adjusted for multiple confounders. The analyses were then performed separately among individuals with different OP susceptibility, indexed by standard polygenetic risk scores(PRS) for OP. Our secondary outcome was OP with pathologic fracture. Subgroup and sensitivity analyses were performed. Additionally, attributable risk percent in the exposed population (AR%) and population attributable fraction (PAF) of sleep behaviors were calculated. Results: Over a median follow-up of 13.7 years, 8253 new-onset OP cases were documented. Unhealthy sleep behaviors, such as long or short sleep duration, insomnia, daytime napping, morning wake-up difficulties, and unhealthy sleep patterns, were associated with elevated risks of OP (HRs ranging from 1.14 to 1.46, all P-value <0.001) compared to healthy sleep behaviors. Similar associations were observed for OP with pathologic fractures. Insomnia exhibited the largest AR% of 39.98 % (95%CI: 36.46, 43.31) and PAF of 33.25 % (95%CI: 30.00, 36.34) among healthy sleep patterns and components. A statistically significant multiplicative interaction was noted between sleep behaviors and OP PRS on OP risk (all P-interaction <0.001). Conclusions: Four unhealthy sleep behaviors and sleep behavior patterns were associated to increased OP risk, with insomnia contributing the most to OP incidence, while genetic risk for OP modified this association. These findings underscore the crucial role of adhering to healthy sleep behaviors for effective OP prevention.
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页数:10
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