Abstract
Background: Maternal thyroid dysfunction during pregnancy has been associated with adverse outcomes for both the mother and child. For this reason, it is important to understand thyroid status in pregnant women. However, there are relatively few published studies that examine thyroid function tests (TFT) and thyroid autoimmunity in non-Western pregnant women.
Methods: Serum samples were longitudinally collected throughout pregnancy from 108 Korean women. TFT, thyroid peroxidase antibodies (TPO-Ab), and thyroglobulin antibodies (Tg-Ab) testing was performed. The impact of gestational age on TPO-Ab and Tg-Ab levels was evaluated and gestational age-specific reference intervals for TFT were established in antibody negative women.
Results: In the first trimester, TPO-Ab and Tg-Ab were positive in 13.9% and 16.7% of women, respectively. For antibody positive women, median autoantibody levels for TPO-Ab and Tg-Ab dropped from first trimester to near term (133.7–10.5 IU/mL, and 162.1–21.9 IU/mL, respectively). Antibody status influenced thyroid stimulating hormone (TSH) during the first trimester, and TSH, free T4 (FT4) and total T4 (TT4) in the early second trimester. Later in gestation, no significant differences in TFT were found based on antibody status. Gestational age-specific reference intervals for TFT were calculated in antibody negative women.
Conclusions: Laboratory evidence of autoimmune thyroid disease (AITD) is common in this population of pregnant Korean women. Antibody status influences TFT values in the first and early second trimester. Thyroid autoantibody status and titer change in an individual-specific manner throughout pregnancy. Gestational age-specific reference intervals should be utilized for interpretation of TFT results in pregnant women.
The authors would like to thank the patients who participated in this study, and Dr. Haiyoung Jung for her review of the manuscript. Reagents to perform this study were supplied by Abbott Diagnostics.
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. Employment, stock ownership and supply of the reagents played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
Research funding: None declared.
Employment or leadership: F. Quinn (Abbott Laboratories); J. Park (Hamni Medicare).
Honorarium: None declared.
Stock ownership: F. Quinn (Abbott Laboratories)
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©2013 by Walter de Gruyter Berlin Boston
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Articles in the same Issue
- Letters to the Editor
- The addition of MESNA in vitro prolongs prothrombin time similar to N-acetyl cysteine
- Detection of unknown β-thalassemia cases from atypical HbA1c chromatograms
- Analytical study of a new turbidimetric assay for urinary neutrophil gelatinase-associated lipocalin (NGAL) determination
- The rare bipolar-contracted red cell significance and correlation with red cell volume
- Howell-Jolly body interference in reticulocyte counts
- PBMC expressed adiponectin mRNA is predictive of survival in patients with gastric cancer
- Comparison study of two commercially available methods for the determination of infliximab, adalimumab, etanercept and anti-drug antibody levels
- Development and validation of a rapid and reliable high-performance liquid chromatography method for methadone quantification in human plasma and saliva
- Reply to Ruiz-Argüello et al.: Comparison study of two commercially available methods for the determination of infliximab, adalimumab, etanercept and anti-drug antibody levels
- Still more discussion on the journal impact factor
- The order of draw, myth or science
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- Masthead
- Editorial
- Multidisciplinarity and interdisciplinarity at work: the prenatal diagnosis
- Research Articles
- Prenatal diagnosis of inherited diseases: 20 years’ experience of an Italian Regional Reference Centre
- Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases
- Prenatal diagnosis of cystic fibrosis: an experience of 181 cases
- Prenatal diagnosis of haemophilia: our experience of 44 cases
- Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy
- Editorials
- Journal impact factor: the debate continues
- Estimation of uncertainty in measurements in the clinical laboratory
- Review
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- Opinion Paper
- More discussion on journal impact factor
- General Clinical Chemistry and Laboratory Medicine
- Category-specific uncertainty modeling in clinical laboratory measurement processes
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- Longitudinal evaluation of thyroid autoimmunity and function in pregnant Korean women
- Evaluation of the N Latex free light chain assay in the diagnosis and monitoring of AL amyloidosis
- Identification of an important potential confound in CSF AD studies: aliquot volume
- Cancer Diagnostics
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- Quantification of EGFR autoantibodies in the amplification phenomenon of HER2 in breast cancer
- Diabetes
- SAA1 genetic polymorphisms are associated with plasma glucose concentration in non-diabetic subjects
- Acknowledgment
- Acknowledgment