Why the study?
Does the use of repetitive follow-up 24-hour urine samples compared to a single baseline measurement change the association between estimated sodium intake and long-term cardiorenal outcomes?
Does the use of repetitive follow-up 24-hour urine samples compared to a single baseline measurement change the association between estimated sodium intake and long-term cardiorenal outcomes?
Using multiple 24-hour urine collections over time significantly alters the estimated association between sodium intake and long-term cardiorenal outcomes compared to relying on a single baseline measurement.
Single baseline sodium estimates risk misclassification in observational studies; leaves open whether repeated measures improve cardiorenal risk prediction.
BACKGROUND: A decrease in sodium intake has been shown to lower blood pressure, but data from cohort studies on the association with cardiovascular and renal outcomes are inconsistent. In these studies, sodium intake was often estimated with a single baseline measurement, which may be inaccurate considering day-to-day changes in sodium intake and sodium excretion. We compared the effects of single versus repetitive follow-up 24-hour urine samples on the relation between sodium intake and long-term cardiorenal outcomes. Sodium intake was estimated with a single baseline collection and the average of samples collected during a 1-, 5-, and 15-year follow-up. We used Cox regression analysis and the landmark approach to investigate the relation between sodium intake and cardiovascular (cardiovascular events or mortality) and renal (end-stage renal disease: dialysis, transplantation, and/or >60% estimated glomerular filtration rate decline, or mortality) outcomes. However, relative to a single baseline measurement, 50% of the subjects had a >0.8-g (>34-mmol) difference in sodium intake with long-term estimations. As a result, 45%, 49%, and 50% of all subjects switched between tertiles of sodium intake when the 1-, 5-, or 15-year average was used, respectively. Consequently, hazard ratios for cardiorenal outcome changed up to 85% with the use of sodium intake estimations from short-term (1-year) and long-term (5-year) follow-up instead of baseline estimations. CONCLUSIONS: Relative to a single baseline 24-hour sodium measurement, the use of subsequent 24-hour urine samples resulted in different estimations of an individual's sodium intake, whereas population averages remained similar. This finding had significant consequences for the association between sodium intake and long-term cardiovascular and renal outcomes.
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Engberink et al. (2017) studied this question.
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