Centre for Community Medicine, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India.
Department of Cardiac Biochemistry, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India.
Natl Med J India. 2022 Jan-Feb;35(1):4-10. doi: 10.25259/NMJI_352_19.
Background Dietary salt intake is an important modifiable risk factor for cardiovascular diseases. Estimation of 24-hour salt intake using morning urine samples needs to be validated in the Indian context. We examined the performance of INTERSALT, Tanaka and Kawasaki equations for the estimation of 24-hour urinary sodium from morning fasting urine (MFU) samples. Methods We enrolled 486 adults aged 18-69 years from four regions of India with equal rural/urban and sex representation to provide 24-hour urine samples. The next day, a MFU sample was obtained. Based on the volume and sodium content of the 24-hour urine sample, 24-hour sodium excretion (reference method) was calculated. Sodium levels in the MFU samples were measured along with other parameters required, and the above equations were used to estimate 24-hour urinary sodium levels. Intraclass correlation coefficient (ICC) was used to assess the degree of agreement between the estimates from the reference method and the three equations. Bland-Altman (BA) plots were used to identify systematic bias and limits of agreement. A difference of 1 g of salt (0.39 g of sodium) between the mean salt intake by 24-hour urine and as estimated by equations was considered acceptable. Results A total of 346 participants provided both the samples. The mean (SD) daily salt intake estimated by the 24-hour urine sample method was 9.9 (5.8) g. ICC was low for all the three equations: highest for Kawasaki (0.16; 95% CI 0.05-0.26) and least for Tanaka (0.12; 0.02-0.22). Only Tanaka equation provided estimates within 1 g of measured 24-hour salt intake (-0.36 g). BA plots showed that as the mean values increased, all the three equations provided lower estimates of salt intake. Conclusion Tanaka equation provided acceptable values of 24-hour salt intake at the population level. However, poor performance of all the equations highlights the need to understand the reasons and develop better methods for the measurement of sodium intake at the population level.
膳食盐摄入量是心血管疾病的一个重要可改变风险因素。在印度,需要对使用晨空腹尿液(MFU)样本估计 24 小时盐摄入量进行验证。我们检验了 INTERSALT、Tanaka 和 Kawasaki 方程在估计来自晨空腹尿液(MFU)样本的 24 小时尿钠中的表现。
我们从印度四个地区招募了 486 名年龄在 18-69 岁的成年人,在城乡和性别上均有代表,以提供 24 小时尿液样本。第二天,采集了一份 MFU 样本。根据 24 小时尿液样本的体积和钠含量,计算 24 小时尿钠排泄量(参考方法)。测量 MFU 样本中的钠水平以及其他所需参数,并使用上述方程估计 24 小时尿钠水平。使用组内相关系数(ICC)评估参考方法和三个方程的估计值之间的一致性程度。Bland-Altman(BA)图用于识别系统偏差和一致性界限。24 小时尿液和方程估计的盐摄入量之间相差 1 克(0.39 克钠)被认为是可以接受的。
共有 346 名参与者同时提供了这两种样本。通过 24 小时尿液样本方法估计的平均(SD)日盐摄入量为 9.9(5.8)克。三个方程的 ICC 均较低:Kawasaki 方程最高(0.16;95%CI 0.05-0.26),Tanaka 方程最低(0.12;0.02-0.22)。只有 Tanaka 方程的估计值在测量的 24 小时盐摄入量的 1 克以内(-0.36 克)。BA 图显示,随着平均值的增加,所有三个方程都提供了较低的盐摄入量估计值。
在人群水平上,Tanaka 方程提供了可接受的 24 小时盐摄入量值。然而,所有方程的表现均较差,这突显了在人群水平上需要了解测量钠摄入量的原因并开发更好的方法。