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Journal of the Endocrine Society logoLink to Journal of the Endocrine Society
. 2019 Apr 30;3(Suppl 1):OR11-1. doi: 10.1210/js.2019-OR11-1

OR11-1 A Randomized Trial of Preconception Levothyroxine in Euthyroid Women with Thyroid Peroxidase Antibodies

Rima Dhillon-Smith 17, Lee Middleton 17, Kirandeep Sunner 17, Versha Cheed 17, Krys Baker 19, Samantha Farrell-Carver 17, Ruth Bender-Atik 11, Rina Agrawal 15, Kalsang Bhatia 2, Edmond Edi-Osagie 8, Tarek Ghobara 15, Pratima Gupta 14, Davor Jurkovic 13, Yacoub Khalaf 3, Marjory MacLean 16, Christopher McCabe 17, Khashia Mulbagal 7, Natalie Nunes 20, Caroline Overton 10, Siobhan Quenby 15, Raj Rai 9, Nick Raine-Fenning 18, Lynne Robinson 1, Jackie Ross 4, Andrew Sizer 12, Rachel Small 14, Alex Tan 6, Martyn Underwood 12, Mark Kilby 17, Kristien Boelaert 17, Jane Daniels 18, Shakila Thangaratinam 6, Shiao Chan 5, Arri Coomarasamy 17
PMCID: PMC6570713

Abstract

BACKGROUND Thyroid peroxidase antibodies are associated with increased risk of miscarriage and preterm birth, even when thyroid function is normal. Small trials indicate levothyroxine could reduce such adverse outcomes. METHODS We conducted a double-blind, placebo-controlled trial to investigate whether levothyroxine treatment would increase live birth rates among euthyroid women with thyroid peroxidase antibodies and a history of miscarriage or infertility. We randomly assigned women to receive 50mcg daily of levothyroxine or placebo, commenced preconception and continued until the end of pregnancy. The primary outcome was live birth ≥34 weeks gestation. RESULTS We tested 19,585 women for thyroid peroxidase antibodies and thyroid function across 49 hospitals in the United Kingdom. A total of 952 women were randomly assigned to receive either levothyroxine (476) or placebo (476). The follow-up rate for the primary outcome was 98.7% (940/952). A pregnancy was achieved in 266/470 (56.6%) in the levothyroxine group and 274/470 (58.3%) in the placebo group. The live birth rate in the levothyroxine group was 37.4% (176/470) versus 37.9% (178/470) in the placebo group (relative risk, 0.97; 95% confidence interval [CI], 0.83 to 1.14, p=0.74; absolute risk difference, -0.4%; 95% CI, -6.6% to 5.8%). There were no significant differences in other pregnancy outcomes, including the rates of pregnancy loss, preterm birth, or in neonatal outcomes. Serious adverse events occurred in 6% of women in the levothyroxine group and 4% in the placebo group (p=0.14). CONCLUSION Treatment with levothyroxine in euthyroid women with thyroid peroxidase antibodies did not increase the rate of live births. Unless otherwise noted, all abstracts presented at ENDO are embargoed until the date and time of presentation. For oral presentations, the abstracts are embargoed until the session begins. Abstracts presented at a news conference are embargoed until the date and time of the news conference. The Endocrine Society reserves the right to lift the embargo on specific abstracts that are selected for promotion prior to or during ENDO.


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