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Published on: April 23, 2019
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.
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.
Introduction:
The current study investigated the value of urine selenium (Se) concentration as a biomarker of population Se status in rural sub-Saharan Africa.
Method:
Urine and plasma Se concentrations were measured among children aged 6-59 months (n = 608) and women of reproductive age (WRA, n = 781) living in rural Zimbabwe (Murehwa, Shamva, and Mutasa districts) and participating in a pilot national micronutrient survey. Selenium concentrations were measured by inductively coupled plasma-mass spectrometry (ICP-MS), and urine concentrations were corrected for hydration status.
Results:
The median (Q1, Q3) urine Se concentrations were 8.4 μg/L (5.3, 13.5) and 10.5 μg/L (6.5, 15.2) in children and WRA, respectively. There was moderate evidence for a relationship between urine Se concentration and plasma Se concentration in children (p = 0.0236) and WRA (p = < 0.0001), but the relationship had poor predictive value. Using previously defined thresholds for optimal activity of iodothyronine deiodinase (IDI), there was an association between deficiency when indicated by plasma Se concentrations and urine Se concentrations among WRA, but not among children.
Discussion:
Urine Se concentration poorly predicted plasma Se concentration at sub-district scales in Zimbabwe, limiting its value as a biomarker of population Se status in this context. Further research is warranted at wider spatial scales to determine the value of urine Se as a biomarker when there is greater heterogeneity in Se exposure.
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