Department of Diabetes, Endocrinology and Clinical Immunology, School of Medicine Hyogo Medical University Nishinomiya Hyogo Japan.
Department of Biostatistics, School of Medicine Hyogo Medical University Nishinomiya Hyogo Japan.
J Am Heart Assoc. 2022 Oct 4;11(19):e024948. doi: 10.1161/JAHA.121.024948. Epub 2022 Sep 21.
Background Although co-occurrence of sleep disorder with heart failure is known, it is not clear whether that condition is a cause or consequence of heart failure. The present study was conducted as a longitudinal examination of the predictive value of sleep parameters on progression of left ventricular diastolic dysfunction. Methods and Results Four-hundred fifty-two subjects were followed for a mean of 34.7 months. An outcome of diastolic dysfunction was defined as increase in early inflow velocity/early diastolic tissue velocity >14. Sleep apnea-hypopnea index, minimal oxygen saturation, sleep duration, and activity index (physical movement during sleep time, a potential parameter of poor sleep quality) were determined using apnomonitor and actigraphy findings, while heart rate variability was measured with a 24-hour active tracer device. Sixty-six of the patients developed diastolic dysfunction during the follow-up period, with a median time of 25 months. Kaplan-Meier analysis results revealed that those with sleep apnea classified as moderate (apnea-hypopnea index 15 to <30, <0.01 versus none) or severe (apnea-hypopnea index ≥30, <0.01 versus none), and with a high activity index (Q3 or Q4, <0.01 versus Q1), but not short sleep duration (=0.27) had a significantly greater risk for a diastolic dysfunction event. Results of multivariable Cox proportional hazards regression analysis indicated that moderate to severe sleep apnea after a follow-up period of 3 years (hazard ratio [HR], 9.26 [95% CI, 1.89-45.26], <0.01) and high activity index (HR, 1.85 [95% CI, 1.01-3.39], =0.04) were significantly and independently associated with future diastolic dysfunction. Moreover, significant association of high activity index with the outcome was not confounded by either minimal oxygen saturation or heart rate variability. Conclusions Sleep apnea and physical movement during sleep, but not sleep duration and autonomic nervous dysfunction, are independent important predictors for progression of left ventricular diastolic dysfunction.
尽管睡眠障碍与心力衰竭同时发生,但尚不清楚该情况是心力衰竭的原因还是结果。本研究对睡眠参数对左心室舒张功能障碍进展的预测价值进行了纵向检查。
452 例患者的平均随访时间为 34.7 个月。舒张功能障碍的结果定义为早期流入速度/早期舒张组织速度增加>14。使用睡眠呼吸暂停-低通气指数、最低氧饱和度、睡眠持续时间和活动指数(睡眠期间的身体运动,这是睡眠质量差的一个潜在参数)来确定睡眠呼吸暂停,而心率变异性则使用 24 小时主动示踪设备进行测量。在随访期间,有 66 例患者发生舒张功能障碍,中位数时间为 25 个月。Kaplan-Meier 分析结果显示,睡眠呼吸暂停中度(呼吸暂停-低通气指数 15 至<30,<0.01 与无)或重度(呼吸暂停-低通气指数≥30,<0.01 与无),以及活动指数高(Q3 或 Q4,<0.01 与 Q1)的患者发生舒张功能障碍事件的风险显著更高。多变量 Cox 比例风险回归分析结果表明,随访 3 年后中度至重度睡眠呼吸暂停(危险比[HR],9.26[95%CI,1.89-45.26],<0.01)和高活动指数(HR,1.85[95%CI,1.01-3.39],=0.04)与未来舒张功能障碍显著相关。此外,高活动指数与结局的显著相关性不受最低氧饱和度或心率变异性的干扰。
睡眠呼吸暂停和睡眠期间的身体运动,但不是睡眠持续时间和自主神经功能障碍,是左心室舒张功能障碍进展的独立重要预测因素。