Shahram Nikbakhtian, Angus B Reed, Bernard Dillon Obika, Davide Morelli, Adam C Cunningham, Mert Aral, David Plans
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A total of 3172 cases of CVD were reported during a mean follow-up period of 5.7 (±0.49) years. An age- and sex-controlled base analysis found that sleep onset time of 10:00 p.m.-10:59 p.m. was associated with the lowest CVD incidence. An additional model, controlling for sleep duration, sleep irregularity, and established CVD risk factors, did not attenuate this association, producing hazard ratios of 1.24 (95% confidence interval, 1.10-1.39; <i>P</i> < 0.005), 1.12 (1.01-1.25; <i>P</i> <i>=</i> 0.04), and 1.25 (1.02-1.52; <i>P</i> <i>=</i> 0.03) for sleep onset <10:00 p.m., 11:00 p.m.-11:59 p.m., and ≥12:00 a.m., respectively, compared to 10:00 p.m.-10:59 p.m. Importantly, sensitivity analyses revealed this association with increased CVD risk was stronger in females, with only sleep onset <10:00 p.m. significant for males.</p><p><strong>Conclusions: </strong>Our findings suggest the possibility of a relationship between sleep onset timing and risk of developing CVD, particularly for women. We also demonstrate the potential utility of collecting information about sleep parameters via accelerometry-capable wearable devices, which may serve as novel cardiovascular risk indicators.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"2 4","pages":"658-666"},"PeriodicalIF":3.9000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/df/40/ztab088.PMC9708010.pdf","citationCount":"27","resultStr":"{\"title\":\"Accelerometer-derived sleep onset timing and cardiovascular disease incidence: a UK Biobank cohort study.\",\"authors\":\"Shahram Nikbakhtian, Angus B Reed, Bernard Dillon Obika, Davide Morelli, Adam C Cunningham, Mert Aral, David Plans\",\"doi\":\"10.1093/ehjdh/ztab088\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>Growing evidence suggests that poor sleep health is associated with cardiovascular risk. However, research in this area often relies upon recollection dependent questionnaires or diaries. Accelerometers provide an alternative tool for measuring sleep parameters objectively. This study examines the association between wrist-worn accelerometer-derived sleep onset timing and cardiovascular disease (CVD).</p><p><strong>Methods and results: </strong>We derived sleep onset and waking up time from accelerometer data collected from 103 712 UK Biobank participants over a period of 7 days. From this, we examined the association between sleep onset timing and CVD incidence using a series of Cox proportional hazards models. A total of 3172 cases of CVD were reported during a mean follow-up period of 5.7 (±0.49) years. An age- and sex-controlled base analysis found that sleep onset time of 10:00 p.m.-10:59 p.m. was associated with the lowest CVD incidence. An additional model, controlling for sleep duration, sleep irregularity, and established CVD risk factors, did not attenuate this association, producing hazard ratios of 1.24 (95% confidence interval, 1.10-1.39; <i>P</i> < 0.005), 1.12 (1.01-1.25; <i>P</i> <i>=</i> 0.04), and 1.25 (1.02-1.52; <i>P</i> <i>=</i> 0.03) for sleep onset <10:00 p.m., 11:00 p.m.-11:59 p.m., and ≥12:00 a.m., respectively, compared to 10:00 p.m.-10:59 p.m. Importantly, sensitivity analyses revealed this association with increased CVD risk was stronger in females, with only sleep onset <10:00 p.m. significant for males.</p><p><strong>Conclusions: </strong>Our findings suggest the possibility of a relationship between sleep onset timing and risk of developing CVD, particularly for women. 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引用次数: 27
摘要
目的:越来越多的证据表明,睡眠健康状况不佳与心血管疾病风险有关。然而,这一领域的研究往往依赖于依赖回忆的问卷调查或日记。加速度计为客观测量睡眠参数提供了另一种工具。本研究探讨了腕带加速计产生的睡眠开始时间与心血管疾病(CVD)之间的关系。方法和结果:我们从103712名英国生物银行参与者收集的加速度计数据中得出了7天内的睡眠开始时间和醒来时间。由此,我们使用一系列Cox比例风险模型检验了睡眠开始时间与心血管疾病发病率之间的关系。在平均5.7(±0.49)年的随访期间,共报告了3172例CVD病例。一项年龄和性别控制的基础分析发现,晚上10点至10点59分的睡眠时间与最低的心血管疾病发病率相关。另一个控制睡眠时间、睡眠不规律和已建立的心血管疾病危险因素的模型并没有减弱这种关联,产生的风险比为1.24(95%置信区间,1.10-1.39;P = 0.04), P = 1.25 (1.02-1.52;P = 0.03)结论:我们的研究结果表明,睡眠开始时间与发生心血管疾病的风险之间可能存在关联,尤其是对女性而言。我们还展示了通过具有加速度计功能的可穿戴设备收集睡眠参数信息的潜在效用,这可能作为新的心血管风险指标。
Accelerometer-derived sleep onset timing and cardiovascular disease incidence: a UK Biobank cohort study.
Aims: Growing evidence suggests that poor sleep health is associated with cardiovascular risk. However, research in this area often relies upon recollection dependent questionnaires or diaries. Accelerometers provide an alternative tool for measuring sleep parameters objectively. This study examines the association between wrist-worn accelerometer-derived sleep onset timing and cardiovascular disease (CVD).
Methods and results: We derived sleep onset and waking up time from accelerometer data collected from 103 712 UK Biobank participants over a period of 7 days. From this, we examined the association between sleep onset timing and CVD incidence using a series of Cox proportional hazards models. A total of 3172 cases of CVD were reported during a mean follow-up period of 5.7 (±0.49) years. An age- and sex-controlled base analysis found that sleep onset time of 10:00 p.m.-10:59 p.m. was associated with the lowest CVD incidence. An additional model, controlling for sleep duration, sleep irregularity, and established CVD risk factors, did not attenuate this association, producing hazard ratios of 1.24 (95% confidence interval, 1.10-1.39; P < 0.005), 1.12 (1.01-1.25; P= 0.04), and 1.25 (1.02-1.52; P= 0.03) for sleep onset <10:00 p.m., 11:00 p.m.-11:59 p.m., and ≥12:00 a.m., respectively, compared to 10:00 p.m.-10:59 p.m. Importantly, sensitivity analyses revealed this association with increased CVD risk was stronger in females, with only sleep onset <10:00 p.m. significant for males.
Conclusions: Our findings suggest the possibility of a relationship between sleep onset timing and risk of developing CVD, particularly for women. We also demonstrate the potential utility of collecting information about sleep parameters via accelerometry-capable wearable devices, which may serve as novel cardiovascular risk indicators.