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Dose Dependency and a Functional Cutoff for TPO-Antibody Positivity During Pregnancy
Author(s) -
Tim I.M. Korevaar,
Victor J.M. Pop,
Layal Chaker,
Mariëtte Goddijn,
Yolanda B. de Rijke,
Peter H. Bisschop,
Maarten A.C. Broeren,
Vincent W. V. Jaddoe,
Marco Medici,
Theo J. Visser,
Eric A.P. Steegers,
Tanja G. M. Vrijkotte,
Robin P. Peeters
Publication year - 2017
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2017-01560
Subject(s) - medicine , thyroid function , pregnancy , population , prospective cohort study , gestation , thyroid peroxidase , obstetrics , cutoff , thyroid function tests , thyroid , endocrinology , environmental health , genetics , biology , physics , quantum mechanics
Objective To investigate a dose dependency of thyroperoxidase antibody (TPOAb) concentrations in relation to thyroid function and premature delivery and define a population-based, pregnancy-specific, functional cutoff for TPOAb positivity. Design Individual participant meta-analysis of three prospective birth cohorts: the Amsterdam Born Children and their Development study, and the Holistic Approach to Pregnancy. Setting Population-based studies in the Netherlands (2002 to 2014). Participants A total of 11,212 pregnant women (<20 weeks’ gestation). Main Outcome Measures Thyrotropin (TSH) and FT4 concentrations, premature delivery. Results In all cohorts, there was a dose-dependent positive association of TPOAb concentrations with TSH concentrations, as well as a dose-dependent negative association with FT4 concentrations during early pregnancy (all P < 0.0001). There was a dose-dependent association of TPOAb concentrations with the risk of premature delivery, which was also modified by TSH concentrations. Women with TPOAb concentrations from the 92nd percentile upward had a higher TSH and a higher risk of a TSH >2.5 mU/L (range, 19.4% to 51.3%). Stratified analyses showed that women with TPOAb concentrations below manufacturer cutoffs already had a higher risk of premature delivery, especially when TSH concentrations were high or in the high-normal range. Conclusions This study demonstrated a dose-dependent relationship between TPOAbs and thyroid function as well as the risk of premature delivery. Furthermore, our results indicate that the currently used cutoffs for TPOAb positivity may be too high. Furthermore, the use of a population-based cutoff for TPOAbs may identify women with a clinically relevant extent of thyroid autoimmunity and a higher risk of premature delivery but that would not be considered TPOAb positive or eligible for treatment otherwise.

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