Infant ustekinumab Clearance, Risk of Infection, and Development after exposure during pregnancy.

Pregnancy infant infections inflammatory bowel disease ustekinumab

Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
24 Jan 2024
Historique:
received: 12 11 2023
revised: 11 01 2024
accepted: 12 01 2024
medline: 27 1 2024
pubmed: 27 1 2024
entrez: 26 1 2024
Statut: aheadofprint

Résumé

Evidence on ustekinumab safety in pregnancy is gradually expanding, but its clearance in the postnatal period is unknown. The aim of this study was to investigate ustekinumab concentrations in umbilical cord blood and rates of clearance after birth, as well as how these correlate with maternal drug concentrations, risk of infection, and developmental milestones during the first year of life. Pregnant women with inflammatory bowel disease were prospectively recruited from 19 hospitals in Denmark and the Netherlands between 2018 and 2022. Infant infections leading to hospitalization/antibiotics, and developmental milestones were assessed. Serum ustekinumab concentrations were measured at delivery and specific time-points. Non-linear regression analysis was applied to estimate clearance. In 78 live-born infants from 76 pregnancies, we observed a low risk of adverse pregnancy outcomes and normal developmental milestones. At birth, the median infant:mother ustekinumab ratio was 2.18 (95%CI,1.69-2.81). Mean time to infant clearance was 6.7 (95%CI,6.1-7.3) months. One-in-four infants at 6 months had an extremely low median concentration of 0.015 μg/ml (range:0.005-0.12) . No variation in median ustekinumab concentration was noted between infants with (2.8μg/ml; range,0.4-6.9) and without (3.1μg/ml; range,0.7-11.0) infections during the first year of life (p=0.41). No adverse signals after intrauterine exposure to ustekinumab were observed with respect to pregnancy outcome, infections, or developmental milestones during the first year of life. Infant ustekinumab concentration was not associated with risk of infections. With the ustekinumab clearance profile, live attenuated vaccination from 6 months of age seems of low risk.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Evidence on ustekinumab safety in pregnancy is gradually expanding, but its clearance in the postnatal period is unknown. The aim of this study was to investigate ustekinumab concentrations in umbilical cord blood and rates of clearance after birth, as well as how these correlate with maternal drug concentrations, risk of infection, and developmental milestones during the first year of life.
METHODS METHODS
Pregnant women with inflammatory bowel disease were prospectively recruited from 19 hospitals in Denmark and the Netherlands between 2018 and 2022. Infant infections leading to hospitalization/antibiotics, and developmental milestones were assessed. Serum ustekinumab concentrations were measured at delivery and specific time-points. Non-linear regression analysis was applied to estimate clearance.
RESULTS RESULTS
In 78 live-born infants from 76 pregnancies, we observed a low risk of adverse pregnancy outcomes and normal developmental milestones. At birth, the median infant:mother ustekinumab ratio was 2.18 (95%CI,1.69-2.81). Mean time to infant clearance was 6.7 (95%CI,6.1-7.3) months. One-in-four infants at 6 months had an extremely low median concentration of 0.015 μg/ml (range:0.005-0.12) . No variation in median ustekinumab concentration was noted between infants with (2.8μg/ml; range,0.4-6.9) and without (3.1μg/ml; range,0.7-11.0) infections during the first year of life (p=0.41).
CONCLUSIONS CONCLUSIONS
No adverse signals after intrauterine exposure to ustekinumab were observed with respect to pregnancy outcome, infections, or developmental milestones during the first year of life. Infant ustekinumab concentration was not associated with risk of infections. With the ustekinumab clearance profile, live attenuated vaccination from 6 months of age seems of low risk.

Identifiants

pubmed: 38278191
pii: S1542-3565(24)00083-1
doi: 10.1016/j.cgh.2024.01.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Mette Julsgaard (M)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark,; Center for Molecular Prediction of Inflammatory Bowel Disease [PREDICT], Department of Clinical Medicine, Aalborg University, Copenhagen, Denmark. Electronic address: mjn@clin.au.dk.

Jantien W Wieringa (JW)

Department of Pediatrics, Haaglanden Medical Center, The Hague, The Netherlands; Department of Pediatrics, Division of Paediatric Infectious Diseases and Immunology, Erasmus MC University Medical Center- Sophia Children's Hospital, Rotterdam, the Netherlands.

Simon M D Baunwall (SMD)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Bo M Bibby (BM)

Department of Biostatistics, University of Aarhus, Aarhus, Denmark.

Gertjan J A Driessen (GJA)

Department of Pediatrics, Maastricht University Medical Center, MosaKids Children's Hospital, Maastricht, The Netherlands.

Linda Kievit (L)

Department of Medicine, Gjødstrup Hospital, Gjødstrup, Denmark.

Jacob B Brodersen (JB)

Department of Gastroenterology, Esbjerg Hospital - University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Regional Health Science, University of Southern Denmark, Esbjerg, Denmark.

Anja Poulsen (A)

Digestive Disease Center, Bispebjerg University Hospital, Copenhagen, Denmark.

Jens Kjeldsen (J)

Department of Medical Gastrointestinal Diseases, Odense University Hospital, Odense, Denmark.

Mette M Hansen (MM)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Hai Q Tang (HQ)

Department of Obstetrics and Gynaecology, Aarhus University Hospital, Denmark.

Christina L Balmer (CL)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Henning Glerup (H)

Diagnostic Centre, University Research Clinic for Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.

Jakob B Seidelin (JB)

Herlev Hospital, Department of Gastroenterology and Hepatology, University of Copenhagen, Denmark.

Kent V Haderslev (KV)

Department of Gastroenterology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Lise Svenningsen (L)

Department of Internal Medicine, Horsens Regional Hospital, Horsens, Denmark.

Signe Wildt (S)

Unit of Medical and Surgical Gastroenterology, Hvidovre University Hospital, Hvidovre, Denmark.

Mie A Juel (MA)

Department of Gastroenterology, Esbjerg Hospital - University Hospital of Southern Denmark, Esbjerg, Denmark; Department of Internal Medicine, Vejle Hospital, Vejle, Denmark.

Anders Neumann (A)

Department of Internal Medicine, Viborg Regional Hospital, Viborg, Denmark.

Jens Fuglsang (J)

Department of Obstetrics and Gynaecology, Aarhus University Hospital, Denmark.

Tine Jess (T)

Center for Molecular Prediction of Inflammatory Bowel Disease [PREDICT], Department of Clinical Medicine, Aalborg University, Copenhagen, Denmark; Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, Denmark.

Anne-Mette Hasse (AM)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Christian L Hvas (CL)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark,; Institute of Clinical Medicine, Health, Aarhus University, Denmark.

Jens Kelsen (J)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark,; Institute of Clinical Medicine, Health, Aarhus University, Denmark.

C Janneke van der Woude (C)

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Classifications MeSH