Urine Se concentration poorly predicts plasma Se concentration at sub-district scales in Zimbabwe, limiting its value

Beaula Mutonhodza1, Mavis P Dembedza1, Edward J M Joy2,3

  • 1Department of Nutrition, Dietetics and Food Sciences, University of Zimbabwe, Harare, Zimbabwe.

Frontiers in Nutrition
|February 22, 2024
PubMed

Insights

Urine selenium levels in rural Zimbabwe showed a weak link to overall selenium status. This suggests urine selenium may not be a reliable biomarker for population selenium status in this region.

Area of Science:

  • Nutritional biochemistry
  • Biomarker research
  • Public health nutrition

Background:

  • Selenium (Se) is an essential trace element crucial for human health.
  • Assessing population selenium status is vital for public health interventions, especially in regions like sub-Saharan Africa.
  • Biomarkers such as urine and plasma selenium concentrations are commonly used to evaluate selenium status.

Purpose of the Study:

  • To investigate the utility of urine selenium concentration as a biomarker for assessing population selenium status in rural sub-Saharan Africa.
  • To evaluate the relationship between urine and plasma selenium concentrations in children and women of reproductive age in Zimbabwe.
  • To determine if urine selenium can predict selenium status based on established thresholds for iodothyronine deiodinase activity.

Main Methods:

  • Measured urine and plasma selenium concentrations in 608 children (6-59 months) and 781 women of reproductive age (WRA) in rural Zimbabwe.
  • Utilized inductively coupled plasma-mass spectrometry (ICP-MS) for selenium analysis.
  • Corrected urine selenium concentrations for hydration status and analyzed relationships with plasma selenium and indicators of selenium deficiency.

Main Results:

  • Median urine selenium concentrations were 8.4 μg/L in children and 10.5 μg/L in WRA.
  • A moderate correlation was found between urine and plasma selenium in both groups, but with poor predictive value.
  • An association between selenium deficiency (based on plasma levels) and urine selenium was observed in WRA, but not in children.

Conclusions:

  • Urine selenium concentration demonstrated poor predictive value for plasma selenium at sub-district scales in Zimbabwe.
  • The findings limit the utility of urine selenium as a biomarker for population selenium status in this specific context.
  • Further research is recommended at broader spatial scales to explore the biomarker's value under conditions of greater selenium exposure variability.
Abstract

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