Drug exposure to infants born to mothers taking Elexacaftor, Tezacaftor, and Ivacaftor.


Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
07 2022
Historique:
received: 10 09 2021
revised: 23 11 2021
accepted: 05 12 2021
pubmed: 26 12 2021
medline: 28 7 2022
entrez: 25 12 2021
Statut: ppublish

Résumé

Elexacaftor, tezacaftor, ivacaftor (ETI) have been associated with marked clinical improvements in adults with CF, which appears to be associated with increased fertility. However, maternal and fetal effects of therapy continued during pregnancy are not well understood. We collected maternal blood, infant blood, cord blood, and breast milk from 3 mother-infant pairs from women who elected to remain on ETI therapy while pregnant. Our results demonstrated relatively high levels of ETI in cord blood, suggesting placental transfer of these compounds, as well as low levels of ETI in breast milk and infant blood, suggesting further transfer of these compounds to breast-fed infants in the postnatal period. These data underscore the need for larger studies on the effects of modulator surrounding reproduction.

Identifiants

pubmed: 34952795
pii: S1569-1993(21)02161-5
doi: 10.1016/j.jcf.2021.12.004
pmc: PMC9213569
mid: NIHMS1767874
pii:
doi:

Substances chimiques

Aminophenols 0
Benzodioxoles 0
Chloride Channel Agonists 0
Drug Combinations 0
Indoles 0
Pyrazoles 0
Pyridines 0
Pyrrolidines 0
Quinolones 0
tezacaftor 0
ivacaftor 1Y740ILL1Z
elexacaftor RRN67GMB0V

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

725-727

Subventions

Organisme : NHLBI NIH HHS
ID : P01 HL108808
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK065988
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES010126
Pays : United States

Informations de copyright

Copyright © 2022 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Drs. Trimble and Fortner report the following personal financial relationships with commercial interests relevant to this article within the past 3 years: As faculty in institutions within the CF Therapeutics Development Network, Dr. Trimble and Fortner have been site Principal Investigator on studies for Vertex. Dr. Fortner reports receiving compensation for speaking engagements for Vertex.

Références

J Cyst Fibros. 2018 Nov;17(6):779-782
pubmed: 29866531
J Cyst Fibros. 2021 May;20(3):402-406
pubmed: 33762125
J Cyst Fibros. 2021 May;20(3):399-401
pubmed: 33353860
Lancet. 2019 Nov 23;394(10212):1940-1948
pubmed: 31679946
Matern Child Health J. 2017 Apr;21(4):818-824
pubmed: 27531009
J Cyst Fibros. 2021 Sep;20(5):835-836
pubmed: 33846105
N Engl J Med. 2019 Nov 7;381(19):1809-1819
pubmed: 31697873

Auteurs

Bethany Collins (B)

Division of Pulmonary and Critical Care Medicine, Department of Medicine, Oregon Health & Science University.

Christopher Fortner (C)

Division of Pediatric Pulmonary Medicine, Department of Pediatrics, SUNY Upstate Medical University.

Amanda Cotey (A)

Salem Pediatric Clinic.

Charles R Jr Esther (CRJ)

Division of Pediatric Pulmonology, Department of Pediatrics, University of North Carolina School of Medicine.

Aaron Trimble (A)

Division of Pulmonary and Critical Care Medicine, Department of Medicine, Oregon Health & Science University. Electronic address: trimblea@ohsu.edu.

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Classifications MeSH