Peginterferon beta-1a concentrations in breast milk of lactating multiple sclerosis patients.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 30 08 2021
revised: 08 02 2022
accepted: 19 02 2022
pubmed: 10 3 2022
medline: 18 5 2022
entrez: 9 3 2022
Statut: ppublish

Résumé

Peginterferon beta-1a is an interferon beta-1a formulation that has been pegylated, resulting in a longer half-life than other interferon beta formulations. We examined concentrations of peginterferon beta-1a in breast milk of lactating patients with multiple sclerosis (MS) receiving peginterferon beta-1a as their postpartum disease-modifying therapy. After completion of titration to a full dose of peginterferon beta-1a and following a single full dose peginterferon beta-1a injection (125 µg), breast milk samples (≥10 mL) were collected by 5 women on days 1-14 post injection. Peginterferon beta-1a concentrations in breast milk samples were measured by a qualified enzyme-linked immunosorbent assay (detection threshold: 15 pg/mL). Mean and median daily concentrations and median maximum concentration (C After receiving a single full dose peginterferon beta-1a injection, the maximum breast milk concentration recorded in an individual patient was 126.2 pg/mL (0.00013 µg/mL) on day 6. The remaining patients all had maximum breast milk concentrations <72 pg/mL. The geometric mean of C Minimal concentrations of peginterferon beta-1a were detected in the breast milk samples. These findings may be useful for clinicians considering postpartum MS treatment options.

Sections du résumé

BACKGROUND BACKGROUND
Peginterferon beta-1a is an interferon beta-1a formulation that has been pegylated, resulting in a longer half-life than other interferon beta formulations. We examined concentrations of peginterferon beta-1a in breast milk of lactating patients with multiple sclerosis (MS) receiving peginterferon beta-1a as their postpartum disease-modifying therapy.
METHODS METHODS
After completion of titration to a full dose of peginterferon beta-1a and following a single full dose peginterferon beta-1a injection (125 µg), breast milk samples (≥10 mL) were collected by 5 women on days 1-14 post injection. Peginterferon beta-1a concentrations in breast milk samples were measured by a qualified enzyme-linked immunosorbent assay (detection threshold: 15 pg/mL). Mean and median daily concentrations and median maximum concentration (C
RESULTS RESULTS
After receiving a single full dose peginterferon beta-1a injection, the maximum breast milk concentration recorded in an individual patient was 126.2 pg/mL (0.00013 µg/mL) on day 6. The remaining patients all had maximum breast milk concentrations <72 pg/mL. The geometric mean of C
CONCLUSION CONCLUSIONS
Minimal concentrations of peginterferon beta-1a were detected in the breast milk samples. These findings may be useful for clinicians considering postpartum MS treatment options.

Identifiants

pubmed: 35263702
pii: S2211-0348(22)00215-2
doi: 10.1016/j.msard.2022.103700
pii:
doi:

Substances chimiques

Polyethylene Glycols 3WJQ0SDW1A
Interferon-beta 77238-31-4
peginterferon beta-1a I8309403R0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103700

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Auteurs

Maria Houtchens (M)

Partners Multiple Sclerosis Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA United States. Electronic address: mhoutchens@bwh.harvard.edu.

Tatenda Mahlanza (T)

Partners Multiple Sclerosis Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA United States.

Andrea I Ciplea (AI)

Department of Neurology, St. Josef Hospital - Katholisches Klinikum Bochum, Ruhr University, Bochum, Gudrunstr. 56, 44791 Bochum, Germany. Electronic address: andrea.ciplea@ruhr-uni-bochum.de.

Maria Claudia Manieri (MC)

Neuroscience Institute, College of Arts and Sciences, Georgia State University, Atlanta, GA United States. Electronic address: mmanieri1@student.gsu.edu.

Nancy F Ramia (NF)

Translational Sciences, Early Development Biomarkers, Biogen, Cambridge, MA United States. Electronic address: nancy.ramia@biogen.com.

Yuan Zhao (Y)

Clinical Pharmacology and Pharmacometrics, Biogen, Cambridge, MA United States. Electronic address: yuan.zhao@biogen.com.

Sarah England (S)

US Medical, Biogen, Weston, MA United States. Electronic address: sarah.england@biogen.com.

Robin Avila (R)

US Medical, Biogen, Weston, MA United States. Electronic address: robin.avilacarey@biogen.com.

Arman Altincatal (A)

US Medical, Biogen, Weston, MA United States. Electronic address: arman.altincatal@biogen.com.

Megan Vignos (M)

US Medical, Biogen, Weston, MA United States. Electronic address: megan.vignos@biogen.com.

Kerstin Hellwig (K)

Department of Neurology, St. Josef Hospital - Katholisches Klinikum Bochum, Ruhr University, Bochum, Gudrunstr. 56, 44791 Bochum, Germany. Electronic address: kerstin.hellwig@klinikum-bochum.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH