Hla Khin Mae, Young Terry, Finn Laurel, Peppard Paul E, Szklo-Coxe Mariana, Stubbs Maryan
Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705-2276, USA.
Sleep. 2008 Jun;31(6):795-800. doi: 10.1093/sleep/31.6.795.
The association of sleep-disordered breathing (SDB) and blunting of normal nocturnal lowering of blood pressure (BP) (nondipping) has only been examined cross-sectionally. The purpose of this study is to investigate whether SDB is prospectively associated with nondipping.
The longitudinal association between SDB and incident nondipping was examined in a subsample of 328 adults enrolled in the Wisconsin Sleep Cohort Study who completed 2 or more 24-hour ambulatory BP studies over an average of 7.2 years of follow-up. SDB identified by baseline in-laboratory polysomnography was defined by apnea-hypopnea index (AHI) categories. Systolic and diastolic nondipping was defined by systolic and diastolic sleep-wake BP ratios > 0.9. All models were adjusted for age, sex, body mass index at baseline and follow-up, smoking, alcohol consumption, hypertension, sleep time, length of follow-up time, and antihypertensive medication use.
There was a dose-response increased odds of developing systolic nondipping in participants with SDB. The adjusted odds ratios (95% confidence interval) of incident systolic nondipping for baseline AHI 5 to < 15 and AHI > or = 15, versus AHI < 5, were 3.1 (1.3-7.7) and 4.4 (1.2-16.3), respectively (P trend = 0.006). The adjusted odds ratios (95% confidence interval) of incident diastolic nondipping for corresponding SDB categories were not statistically significant: 2.0 (0.8-5.6) and 1.3 (0.2-7.1).
Our longitudinal findings of a dose-response increase in development of systolic nondipping of BP with severity of SDB at baseline in a population-based sample provide evidence consistent with a causal link. Nocturnal systolic nondipping may be a mechanism by which SDB contributes to increased cardiovascular disease.
睡眠呼吸紊乱(SDB)与正常夜间血压(BP)下降减弱(非勺型)之间的关联仅进行过横断面研究。本研究旨在探讨SDB是否与非勺型存在前瞻性关联。
在威斯康星睡眠队列研究的328名成年人亚组中,研究SDB与新发非勺型之间的纵向关联,这些参与者在平均7.2年的随访期间完成了2次或更多次24小时动态血压研究。通过基线实验室多导睡眠图确定的SDB由呼吸暂停低通气指数(AHI)类别定义。收缩压和舒张压非勺型由收缩压和舒张压睡眠-清醒血压比值>0.9定义。所有模型均根据年龄、性别、基线和随访时的体重指数、吸烟、饮酒、高血压、睡眠时间、随访时间长度以及抗高血压药物使用情况进行了调整。
SDB参与者发生收缩压非勺型的几率呈剂量反应增加。基线AHI为5至<15以及AHI>或=15的参与者发生收缩压非勺型的调整优势比(95%置信区间)与AHI<5的参与者相比,分别为3.1(1.3 - 7.7)和4.4(1.2 - 16.3)(P趋势 = 0.006)。相应SDB类别的新发舒张压非勺型的调整优势比(95%置信区间)无统计学意义:2.0(0.8 - 5.6)和1.3(0.2 - 7.1)。
我们在基于人群的样本中进行的纵向研究发现,基线时SDB严重程度与血压收缩压非勺型发展呈剂量反应增加,这一发现提供了与因果关系一致的证据。夜间收缩压非勺型可能是SDB导致心血管疾病增加的一种机制。