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Relationship between metabolic syndrome, circadian treatment time, and blood pressure non-dipping profile in essential hypertension

机译:代谢综合征,昼夜节律治疗时间和原发性高血压患者血压非浸润状态之间的关系

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There is a strong association between metabolic syndrome (MS) and increased cardiovascular risk. Moreover, elevated nighttime blood pressure (BP) and non-dipping (subjects with <10% decline in the asleep relative to the awake BP mean) have been also linked to increased cardiovascular morbidity and mortality. We investigated the relation between MS, circadian time of hypertension treatment, and impaired nighttime BP decline in a cross-sectional study on 3352 (1576 men/1776 women) non-diabetic hypertensive subjects, 53.7±13.1 (mean±SD) yrs of age. Among them, 2056 were ingesting all their prescribed hypertension medication upon awakening, and 1296 were ingesting at least one of their BP medications at bedtime. BP was measured by ambulatory monitoring for 48 consecutive hours to substantiate reproducibility of the dipping pattern. Physical activity was simultaneously monitored every minute by wrist actigraphy to accurately calculate mean BP when awake and asleep for each subject. MS was present in 52.6% of the subjects. The prevalence of an altered non-dipper BP profile was significantly higher among subjects with MS (52.0% vs. 39.5% in subjects without MS, p <.001). Non-dipping was significantly more prevalent among subjects ingesting all BP-lowering medications upon awakening (56.8%) than among those ingesting at least one of their BP medications at bedtime (29.1%; p <.001). Subjects with MS had significantly higher values of uric acid (6.0 vs. 5.3mg/dL, p <.001), plasma fibrinogen (331 vs. 315mg/dL, p <.001), and erythrocyte sedimentation rate (14.8 vs. 12.4mm, p <.001). Non-dipping was significantly associated with the presence of MS and treatment upon awakening in a multiple logistic regression model adjusted by significant confounding factors, including age, creatinine, erythrocyte sedimentation rate, and cigarette smoking. This cross-sectional study documents a significant increase of a blunted sleep-time BP decline in treated hypertensive subjects with MS. Even in the presence of MS, treatment at bedtime is significantly associated with lower prevalence of a high-risk non-dipper BP profile.
机译:代谢综合征(MS)与心血管风险增加之间有很强的联系。此外,夜间血压(BP)升高和不蘸药(相对于清醒BP均值而言,入睡率下降<10%的受试者)也与心血管疾病的发病率和死亡率增加有关。在一项针对5352±13.1岁(平均±SD)岁的非糖尿病高血压受试者的3352名(1576名男性/ 1776名女性)的横断面研究中,我们调查了MS,高血压的昼夜节律时间和夜间BP下降受损之间的关系。 。其中,有2056人在醒来时摄取了所有处方的高血压药物,有1296人在就寝时间摄取了至少一种BP药物。通过连续48小时的动态监测来测量BP,以证实浸入模式的可重复性。腕部活动记录仪每分钟同时监测一次体育锻炼,以准确计算每个受试者清醒和睡着时的平均BP。 MS存在于52.6%的受试者中。患有MS的受试者的非北斗七星BP分布改变的患病率显着更高(52.0%比无MS的受试者为39.5%,p <.001)。与在睡前摄入至少一种BP药物的受试者(29.1%; p <.001)相比,在觉醒时摄入所有降低BP的药物的受试者中,不蘸药的发生率(56.8%)更为普遍。 MS患者的尿酸(6.0 vs. 5.3mg / dL,p <.001),血浆纤维蛋白原(331 vs. 315mg / dL,p <.001)和红细胞沉降率(14.8 vs. 12.4)明显更高毫米,p <.001)。非浸渍与多发性硬化症的存在和唤醒后的治疗密切相关,该模型由年龄,肌酐,红细胞沉降率和吸烟等重大混杂因素调整后的多元逻辑回归模型。这项横断面研究表明,经治疗的MS高血压患者的睡眠时间BP下降明显变钝。即使在MS的存在下,就寝时间的治疗也与高风险的非北斗星BP分布的较低患病率显着相关。

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