Hyperthyroidism in pregnancy: design and methodology of a Danish multicenter study.

Antithyroid Gestation Graves’ disease Levothyroxine Methimazole Propylthiouracil

Journal

Thyroid research
ISSN: 1756-6614
Titre abrégé: Thyroid Res
Pays: England
ID NLM: 101469037

Informations de publication

Date de publication:
12 Jun 2023
Historique:
received: 19 11 2022
accepted: 19 03 2023
medline: 12 4 2023
entrez: 11 4 2023
pubmed: 12 4 2023
Statut: epublish

Résumé

Graves' disease (GD) is the main cause of hyperthyroidism in women of the fertile age. In pregnant women, the disease should be carefully managed and controlled to prevent maternal and fetal complications. Observational studies provide evidence of the adverse effects of untreated hyperthyroidism in pregnancy and have in more recent years substantiated a risk of teratogenic side effects with the use of antithyroid drugs (ATDs). These findings have challenged the clinical recommendations regarding the choice of treatment when patients become pregnant. To extend observational findings and support future clinical practice, a systematic collection of detailed clinical data in and around pregnancy is needed. With the aim of collecting clinical and biochemical data, a Danish multicenter study entitled 'Pregnancy Investigations on Thyroid Disease' (PRETHYR) was initiated in 2021. We here describe the design and methodology of the first study part of PRETHYR. This part focuses on maternal hyperthyroidism and recruits female patients in Denmark with a past or present diagnosis of GD, who become pregnant, as well as women who are treated with ATDs in the pregnancy, irrespective of the underlying etiology. The women are included during clinical management from endocrine hospital departments in Denmark, and study participation includes patient questionnaires in pregnancy and postpartum as well as review of medical records from the mother and the child. Data collection was initiated on November 1, 2021 and covered all five Danish Regions from March 1, 2022. Consecutive study inclusion will continue, and we here report the first status of inclusion. As of November 1, 2022, a total of 62 women have been included in median pregnancy week 19 (interquartile range (IQR): 10-27) with a median maternal age of 31.4 years (IQR: 28.5-35.1). At inclusion, 26 women (41.9%) reported current use of thyroid medication; ATDs (n = 14), Levothyroxine (n = 12). This report describes a newly established systematic and nationwide collection of detailed clinical data on pregnant women with hyperthyroidism and their offspring. Considering the course and relatively low prevalence of GD in pregnant women, such nationwide design is essential to establish a sufficiently large cohort.

Sections du résumé

BACKGROUND BACKGROUND
Graves' disease (GD) is the main cause of hyperthyroidism in women of the fertile age. In pregnant women, the disease should be carefully managed and controlled to prevent maternal and fetal complications. Observational studies provide evidence of the adverse effects of untreated hyperthyroidism in pregnancy and have in more recent years substantiated a risk of teratogenic side effects with the use of antithyroid drugs (ATDs). These findings have challenged the clinical recommendations regarding the choice of treatment when patients become pregnant. To extend observational findings and support future clinical practice, a systematic collection of detailed clinical data in and around pregnancy is needed.
METHODS METHODS
With the aim of collecting clinical and biochemical data, a Danish multicenter study entitled 'Pregnancy Investigations on Thyroid Disease' (PRETHYR) was initiated in 2021. We here describe the design and methodology of the first study part of PRETHYR. This part focuses on maternal hyperthyroidism and recruits female patients in Denmark with a past or present diagnosis of GD, who become pregnant, as well as women who are treated with ATDs in the pregnancy, irrespective of the underlying etiology. The women are included during clinical management from endocrine hospital departments in Denmark, and study participation includes patient questionnaires in pregnancy and postpartum as well as review of medical records from the mother and the child.
RESULTS RESULTS
Data collection was initiated on November 1, 2021 and covered all five Danish Regions from March 1, 2022. Consecutive study inclusion will continue, and we here report the first status of inclusion. As of November 1, 2022, a total of 62 women have been included in median pregnancy week 19 (interquartile range (IQR): 10-27) with a median maternal age of 31.4 years (IQR: 28.5-35.1). At inclusion, 26 women (41.9%) reported current use of thyroid medication; ATDs (n = 14), Levothyroxine (n = 12).
CONCLUSION CONCLUSIONS
This report describes a newly established systematic and nationwide collection of detailed clinical data on pregnant women with hyperthyroidism and their offspring. Considering the course and relatively low prevalence of GD in pregnant women, such nationwide design is essential to establish a sufficiently large cohort.

Identifiants

pubmed: 37041614
doi: 10.1186/s13044-023-00154-8
pii: 10.1186/s13044-023-00154-8
pmc: PMC10088206
doi:

Types de publication

Journal Article

Langues

eng

Pagination

11

Subventions

Organisme : The Novo Nordisk Foundation
ID : NNF20OC0059465

Informations de copyright

© 2023. The Author(s).

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Auteurs

Nanna Maria Uldall Torp (NMU)

Department of Clinical Biochemistry, Aalborg University Hospital, Hobrovej 18-22, Aalborg, 9000, Denmark. nanna.torp@rn.dk.
Department of Clinical Medicine, Aalborg University, Aalborg, Denmark. nanna.torp@rn.dk.

Inge Bülow Pedersen (IB)

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Department of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.

Allan Carlé (A)

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Department of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.

Jesper Scott Karmisholt (JS)

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Department of Endocrinology, Aalborg University Hospital, Aalborg, Denmark.

Eva Ebbehøj (E)

Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.

Diana Grove-Laugesen (D)

Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.

Thomas Heiberg Brix (TH)

Department of Endocrinology, Odense University Hospital, Odense, Denmark.
Institute of Clinical Research, University of Southern Denmark, Odense, Denmark.

Steen Joop Bonnema (SJ)

Department of Endocrinology, Odense University Hospital, Odense, Denmark.
Institute of Clinical Research, University of Southern Denmark, Odense, Denmark.

Bieke F Schrijvers (BF)

Department of Endocrinology, Zealand University Hospital Køge, Køge, Denmark.

Birte Nygaard (B)

Department of Endocrinology, Copenhagen University Hospital Herlev-Gentofte, Herlev, Denmark.
Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark.

Lena Bjergved Sigurd (LB)

Department of Endocrinology, Copenhagen University Hospital Herlev-Gentofte, Herlev, Denmark.
Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark.

Ulla Feldt-Rasmussen (U)

Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark.
Department of Endocrinology and Metabolism, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Marianne Klose (M)

Department of Endocrinology and Metabolism, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Åse Krogh Rasmussen (ÅK)

Department of Endocrinology and Metabolism, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Stig Andersen (S)

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Deparment of Geriatrics, Aalborg University Hospital, Aalborg, Denmark.

Stine Linding Andersen (SL)

Department of Clinical Biochemistry, Aalborg University Hospital, Hobrovej 18-22, Aalborg, 9000, Denmark.
Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Classifications MeSH