Urinary iodine concentrations of pregnant women in Ukraine
-
Yui Sekitani
Abstract
Background: Iodine requirements increase during pregnancy and previous studies have reported the inadequate iodine status of pregnant women in areas that have achieved iodine sufficiency in the general population. We examined the urinary iodine (UI) concentrations of pregnant women in Ukraine, where the iodine status is showing improvement among the general population.
Methods: We enrolled 148 pregnant women <16 weeks pregnant and 80 healthy women as a control group living in Zhitomir, Ukraine. UI concentration, thyroid-stimulating hormone (TSH), antithyroglobulin antibodies (TGAb), and antithyroid peroxidase antibodies (TPOAb) were measured.
Results: The median UI concentrations were significantly lower in pregnant women than in control women [13.0 (ND–51.0) μg/L vs. 62.0 (35.3–108.5) μg/L, p<0.001]. TSH concentrations were significantly lower in pregnant women than in control women [1.7 (1.2–2.7) IU/L vs. 2.2 (1.4–3.1) IU/L, p=0.011], but this difference disappeared when adjusted for age (2.1±0.1 IU/L vs. 2.4±0.2 IU/L, p=0.097). The frequency of TSH over 6.2 IU/L and the frequency of positive TGAb and/or TPOAb were not statistically different between groups (p=0.70 and p=0.48, respectively). The UI concentrations of 142 pregnant women (95.9%) were <150 μg/L indicating insufficient iodine intake.
Conclusions: The UI concentration of pregnant women in Ukraine revealed severe iodine deficiency. Regular monitoring and appropriate nutrition education are essential because iodine deficiency can be easily prevented by adequate iodine intake. The risk of iodine deprivation during pregnancy needs to be assessed locally over time because it may occur in areas that are not globally recognized as being iodine-deficient.
This study was supported by Grant-in-Aid from the Japan Society for the Promotion of Science (No. 19500600) and the Ministry of Education, Culture, Sports, Science and Technology of Japan through the Nagasaki University Global COE program.
Conflict of interest statement
Authors’ conflict of interest disclosure: The authors stated that there are no conflicts of interest regarding the publication of this article.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
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©2013 by Walter de Gruyter Berlin Boston
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Artikel in diesem Heft
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- Missing agreement between the two IMMULITE® PSA assays
- “Cerebrovascular stressing”: dipyridamole-induced S100B elevation predicts ischemic cerebrovascular events
- Discrepancy in lamellar body counts (LBCs) between the Sysmex XE-2100 and Sysmex XT-2000i instruments
- Interphase fluorescent in situ hybridization detection of the 7q11.23 chromosomal inversion in a clinical laboratory: automated versus manual scoring
- Adrenocorticotropic hormone stability in preanalytical phase depends on temperature and proteolytic enzyme inhibitor
- The impact on costs and efficiency of reducing the number of collected tubes
- Improved software on the Sysmex XE-5000 BF mode for counting leukocytes in cerebrospinal fluid
- First trimester placental growth factor and soluble fms-like tyrosine kinase 1 are significantly related to PAPP-A levels
- Preliminary evaluation of complete blood cell count on Mindray BC-6800
- Rational use of laboratory tests: albuminuria
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- Editorials
- Fifty years of CCLM – invitation to join us for a reception in Milan
- Personalized (laboratory) medicine: a bridge to the future
- PSA, PCA3 and the phi losophy of prostate cancer management
- Reviews
- Gender medicine: a task for the third millennium
- Evaluation of [−2] proPSA and Prostate Health Index (phi) for the detection of prostate cancer: a systematic review and meta-analysis
- Harmonization in laboratory medicine: the complete picture
- Opinion Papers
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- Time for a conceptual shift in assessment of internal quality control for whole blood or cell-based testing systems? An evaluation using platelet function and the PFA-100 as a case example
- Guidelines and Recommendations
- A position paper of the EFLM Committee on Education and Training and Working Group on Distance Education Programmes/E-Learning: developing an e-learning platform for the education of stakeholders in laboratory medicine
- General Clinical Chemistry and Laboratory Medicine
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- Reference values and upper reference limits for 26 trace elements in the urine of adults living in Belgium
- Biological variation and reference change values of common clinical chemistry and haematologic laboratory analytes in the elderly population
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- Cancer Diagnostics
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