Thyroid disease

Maternal TSH-receptor antibodies predict fetal/neonatal hyperthyroidism in pregnancies with a history of Graves disease

J Clin Endocrinol MetabPublished Prospective cohort study

Authors' conclusion

Trimester-specific TRAb thresholds were higher than the universal ULN multipliers commonly applied in clinical practice, and differed by gestational age and disease status.

Study context

Population
Pregnant women with a history of or active Graves disease, tertiary and secondary care centres across the Netherlands, 2010–2023; TRAb measured with TRAK human assay on BRAHMS Kryptor Compact Plussecondary care centres 44
Participants
500 vs 178
Exposure
History of Graves disease vs Active Graves
  • History of Graves diseasen = 500
  • Active Gravesn = 178
Outcome
Biochemically confirmed fetal/neonatal hyperthyroidism or hypothyroidism
Methodological detailsmulticentre, observational
  • Multicentre
  • Observational

Main finding

As reported in the abstract

Prediction of fetal/neonatal thyroid dysfunction by trimester-specific TRAb thresholds
GroupTrimester-specific cutoffs (fold upper limit of normal (ULN))NPVSensitivity
History of Graves disease25-, 19-, and 6-fold100%
Active Graves10-, 12-, and 10-fold89%, 86%, and 83%

Trimester-specific cutoffs (fold upper limit of normal (ULN))

History of Graves disease25-, 19-, and 6-fold
Active Graves10-, 12-, and 10-fold

NPV

History of Graves disease100%
Active Graves— not stated in the abstract

Sensitivity

History of Graves disease— not stated in the abstract
Active Graves89%, 86%, and 83%

Observational data: associations, not effects.

Further findings

Neonatal hyperthyroidism with antithyroid drug treatment

Neonatal hyperthyroidism occurred despite low or declining maternal TRAb levels in mothers treated with antithyroid drugs

Original publication

Maternal TSH-receptor antibodies predict fetal/neonatal hyperthyroidism in pregnancies with a history of Graves disease. J Clin Endocrinol Metab. Published 18 March 2026. doi:10.1210/clinem/dgag118

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.