Flinders Health and Medical Research Institute, Sleep Health, Flinders University, Adelaide, SA, Australia.
Flinders Health and Medical Research Institute, Sleep Health, Flinders University, Adelaide, SA, Australia; College of Science and Engineering, Flinders University, Adelaide, SA, Australia.
Chest. 2023 Jul;164(1):231-240. doi: 10.1016/j.chest.2023.01.027. Epub 2023 Jan 28.
Single-night disease misclassification of OSA due to night-to-night variability may contribute to inconsistent findings in OSA trials.
Does multinight quantification of OSA severity provide more precise estimates of associations with incident hypertension?
A total of 3,831 participants without hypertension at baseline were included in simulation analyses. Included participants had ≥ 28 days of nightly apnea-hypopnea index (AHI) recordings via an under-mattress sensor and ≥ three separate BP measurements over a 3-month baseline period followed by ≥ three separate BP measurements 6 to 9 months postbaseline. Incident hypertension was defined as a mean systolic BP ≥ 140 mm Hg or a mean diastolic BP ≥ 90 mm Hg. Simulated trials (1,000) were performed, using bootstrap methods to investigate the effect of variable numbers of nights (x = 1-56 per participant) to quantify AHI and the ability to detect associations between OSA and incident hypertension via logistic regression adjusted for age, sex, and BMI.
Participants were middle-aged (mean ± SD, 52 ± 12 y), mostly male (91%), and overweight (BMI, 28 ± 5 kg/m). Single-night quantification of OSA failed to detect an association with hypertension risk in 42% of simulated trials (α = .05). Conversely, 100% of trials detected an association when AHI was quantified over ≥ 28 nights. Point estimates of hypertension risk were also 50% higher and uncertainty was five times lower during multinight vs single-night simulation trials.
Multinight monitoring of OSA allows for better estimates of hypertension risk and potentially other adverse health outcomes associated with OSA. These findings have important implications for clinical care and OSA trial design.
由于 OSA 的夜间变异性,单晚疾病分类可能导致 OSA 试验的结果不一致。
多晚 OSA 严重程度的量化是否能更准确地估计与高血压事件的相关性?
共有 3831 名基线时无高血压的参与者纳入模拟分析。纳入的参与者在基线期至少有 28 天的夜间呼吸暂停低通气指数(AHI)记录,使用床垫下传感器;在基线期至少有三次独立的血压测量,然后在基线后 6-9 个月至少有三次独立的血压测量。高血压的定义为平均收缩压≥140mmHg 或平均舒张压≥90mmHg。使用 bootstrap 方法进行模拟试验(1000 次),以研究变量数量(每个参与者 1-56 晚)对 AHI 量化的影响,以及通过调整年龄、性别和 BMI 的逻辑回归检测 OSA 与高血压事件之间相关性的能力。
参与者为中老年人(平均±标准差,52±12 岁),主要为男性(91%),超重(BMI,28±5kg/m)。单晚 OSA 量化未能在 42%的模拟试验中检测到与高血压风险的相关性(α=0.05)。相反,当 AHI 被量化为≥28 晚时,100%的试验检测到与高血压的相关性。在多晚与单晚的模拟试验中,高血压风险的点估计值也高出 50%,不确定性低 5 倍。
多晚监测 OSA 可以更好地估计高血压风险以及与 OSA 相关的其他潜在不良健康后果。这些发现对临床护理和 OSA 试验设计具有重要意义。