Del Giorno Rosaria, Ceresa Christos, Gabutti Sofia, Troiani Chiara, Gabutti Luca
Department of Internal Medicine, Clinical Research Unit, Regional Hospital of Bellinzona and Valli, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.
Institute of Biomedicine, University of Southern Switzerland, Lugano, Switzerland.
Diabetes Metab Syndr Obes. 2020 Sep 23;13:3289-3299. doi: 10.2147/DMSO.S266246. eCollection 2020.
Excessive salt intake is an important determinant of cardiovascular (CV) health, impacting arterial stiffness and central blood pressure. However, sodium exhibits several patterns of excretion in urine during day- and night-time, which could differently affect CV risk. Here, we sought to explore the relationship between the day:night urinary sodium excretion ratio and arterial stiffness and central hemodynamics in the general population.
Cross-sectional analysis in 1062 subjects. Arterial stiffness (pulse-wave velocity, PWV), central blood pressure (central systolic blood pressure, cSBP; central diastolic blood pressure, cDBP), and other hemodynamic parameters were noninvasively assessed. Day- and night-time urinary sodium were separately detected. Analyses were performed according to the day:night urinary sodium excretion ratio tertiles (T1-T3).
Low day-time excretors (T1) showed significantly higher values of arterial stiffness when compared with high day-time excretors (T3) (cf-PWV 7.6 ± 1.9 vs 6.9 ± 1.5 m/sec; p ≤ 0.001), and higher central BP parameters (cSBP: 111.6 ± 12.1 vs 109.0 ± 11.1 mmHg, p ≤ 0.001; cDBP, 76.9 ± 9.2 vs 75.1 ± 9.3 mmHg, p ≤ 0.001). In multivariate linear-regression models (β, CI), the day:night ratio of sodium excretion was significantly associated with arterial stiffness (cf-PWV -0.386, -0.559, -0.213, p ≤ 0.001) and with central hemodynamic parameters (cSBP -1.655, -2.800, -0.510; p ≤ 0.001; cDBP -1.319, -2.218, -0.420, p ≤ 0.001). Associations persisted after controlling for multiple confounding factors. In logistic-regression models, the risk of increased arterial stiffness was significantly reduced as the day:night ratio of urinary sodium excretion increased (OR 0.40, 95% CI 0.25-0.65, p ≤ 0.001).
The individual, intra-daily pattern of urinary sodium excretion, characterised by low daytime excretion, is associated with increased arterial stiffness and central blood pressure. Further studies are advocated to clarify the clinical utility of assessing the daily pattern of sodium excretion.
过量盐摄入是心血管(CV)健康的重要决定因素,影响动脉僵硬度和中心血压。然而,钠在白天和夜间的尿排泄呈现几种模式,这可能对心血管风险产生不同影响。在此,我们试图探讨一般人群中昼夜尿钠排泄率与动脉僵硬度和中心血流动力学之间的关系。
对1062名受试者进行横断面分析。无创评估动脉僵硬度(脉搏波速度,PWV)、中心血压(中心收缩压,cSBP;中心舒张压,cDBP)和其他血流动力学参数。分别检测白天和夜间的尿钠。根据昼夜尿钠排泄率三分位数(T1 - T3)进行分析。
与白天高排泄者(T3)相比,白天低排泄者(T1)的动脉僵硬度值显著更高(cf - PWV 7.6 ± 1.9 vs 6.9 ± 1.5米/秒;p≤0.001),且中心血压参数更高(cSBP:111.6 ± 12.1 vs 109.0 ± 11.1 mmHg,p≤0.001;cDBP,76.9 ± 9.2 vs 75.1 ± 9.3 mmHg,p≤0.001)。在多变量线性回归模型(β,CI)中,钠排泄的昼夜比与动脉僵硬度(cf - PWV -0.386,-0.559,-0.213,p≤0.001)和中心血流动力学参数(cSBP -1.655,-2.800,-0.510;p≤0.001;cDBP -1.319,-2.218,-0.420,p≤0.001)显著相关。在控制多个混杂因素后,这种关联仍然存在。在逻辑回归模型中,随着尿钠排泄的昼夜比增加,动脉僵硬度增加的风险显著降低(OR 0.40,95%CI 0.25 - 0.65,p≤0.001)。
以白天排泄低为特征的个体日内尿钠排泄模式与动脉僵硬度增加和中心血压升高有关。提倡进一步研究以阐明评估钠排泄日模式的临床效用。