Abstract
Objective: To compare different possibilities of reporting the iodine supply in the same urine samples. Indeed, in field studies, urinary iodine concentration (I/L: μg I/L, μmol I/L, I/creatinine: μg I/g creatanine, μmol I/mol creatinine) is more readily available than excretion (I/24h μg I/24 h, μmol I/24h). However, confusion exists regarding the comparability of iodine supply based upon I/L, I/creatinine and I/24h, which for decades have been regarded as biochemically equivalent.
Design: We compared I/24h, I/L and I/creatinine in accurate 24 h collections of urine and I/L and I/creatinine in 47 spot urine samples.
Patients: A total of 13 subjects (Bern n=7, Brussels n=6) collected a total of 110 precise 24 h urine collections (Bern n=63, Brussels n=47). The subjects from Brussels also took a spot sample at the beginning of each 24 h collection.
Results: Iodine supply in both places was mildly deficient according to the criteria of WHO; all but one collection indicated an intake of >0.39 μmol I/24h (>50 μg I/24h). The same data presented as I/creatinine (or I/L) indicated an iodine intake of <0.39 (<50 μg I/24h) in 5% (24%) of the samples in Bern and 23% (57%) in Brussels. Similar findings were observed for 47 spot samples. Whatever the cut-off selected, I/creatinine and I/L were systematically lower than I/24h (P<0.0002). Creatinine showed smaller CV than volume but did not perform better in defining iodine intake.
Conclusions: Considering I/24h as a reference, both I/creatinine and I/L clearly underestimate the iodine intake in subjects with adequate proteoenergetic intake. The significant deviations observed illustrate the urgent need for establishing separate ranges for I/24h, I/creatinine and I/L. In population studies, these deviations might even be larger.
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Acknowledgements
This work was supported by grants from the ‘Swiss National Foundation for Scientific Research’, the ‘Fondation Genevoise de Bienfaisance V. Rossi di Montelera’ and the ‘Schüpbach Foundation’. The Fonds de la Recherche Scientifique Médicale Belge (Convention n° 3.4505.97 to P.B.) also supported it.
Presented in part at the 24th annual meeting of the European Thyroid Association (ETA) in Munich, Germany, on 2 September 1997 (Als et al, 1997) and at the 12th IFCC European Congress of Clinical Chemistry in Basel, Switzerland, on 29 August 1997 (Als et al, 1997, The Official Publication of Medlab 97. Proceedings of the European Congress of Clinical Chemistry 1997, 285.)
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Guarantors: PP Bourdoux, Dr C Als.
Contributors: CA was involved in conception and design of the study, acquisition and collection of data, analysis and interpretation of data, and in writing and revising the article; CM performed analysis and interpretation of data, writing the article, and revising the article; DW was involved in acquisition and collection of data, interpretation of data; HVVT in the acquisition and collection of data, analysis of data, interpretation of data, writing and revising the article; HG in the conception and design of the study, interpretation of data, revising the article; and PB was involved in conception and design of the study, acquisition and collection of data, analysis and interpretation of data, writing and revising the article.
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Als, C., Minder, C., Willems, D. et al. Quantification of urinary iodine: a need for revised thresholds. Eur J Clin Nutr 57, 1181–1188 (2003). https://doi.org/10.1038/sj.ejcn.1601740
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DOI: https://doi.org/10.1038/sj.ejcn.1601740
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