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Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin

Triheptanoin is an odd‐carbon, medium‐chain triglyceride consisting of three fatty acids with seven carbons each on a glycerol backbone, indicated for the treatment of adult and pediatric patients with long‐chain fatty acid oxidation disorders (LC‐FAOD). A total of 562 plasma concentrations of hepta...

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Autores principales: Lee, Sun Ku, Gosselin, Nathalie H., Jomphe, Claudia, McKeever, Kathleen, Putnam, Wendy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795984/
https://www.ncbi.nlm.nih.gov/pubmed/35908210
http://dx.doi.org/10.1002/cpdd.1145
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author Lee, Sun Ku
Gosselin, Nathalie H.
Jomphe, Claudia
McKeever, Kathleen
Putnam, Wendy
author_facet Lee, Sun Ku
Gosselin, Nathalie H.
Jomphe, Claudia
McKeever, Kathleen
Putnam, Wendy
author_sort Lee, Sun Ku
collection PubMed
description Triheptanoin is an odd‐carbon, medium‐chain triglyceride consisting of three fatty acids with seven carbons each on a glycerol backbone, indicated for the treatment of adult and pediatric patients with long‐chain fatty acid oxidation disorders (LC‐FAOD). A total of 562 plasma concentrations of heptanoate, the most abundant and pharmacologically active metabolite of triheptanoin, from 13 healthy adult subjects and 30 adult and pediatric subjects with LC‐FAOD were included in the population pharmacokinetic (PK) analyses. Multiple peaks of heptanoate observed in several subjects were characterized by dual first‐order absorption with a lag time in the second absorption compartment. The disposition of heptanoate in human plasma was adequately described by one‐compartmental distribution with a linear elimination. The apparent clearance (CL/F) and apparent volume of distribution were allometrically scaled with body weight to describe PK data across a wide range of age groups in subjects with LC‐FAOD. The typical CL/F in adult subjects with LC‐FAOD was ≈19% lower than that in healthy subjects. Model‐estimated elimination half‐life for LC‐FAOD patients was ∼1.7 hours, supporting a recommended dosing frequency of ≥4 times per day. Covariate analyses indicate that age, race, and sex did not lead to clinically meaningful changes in the exposure of heptanoate.
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spelling pubmed-97959842022-12-28 Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin Lee, Sun Ku Gosselin, Nathalie H. Jomphe, Claudia McKeever, Kathleen Putnam, Wendy Clin Pharmacol Drug Dev Articles Triheptanoin is an odd‐carbon, medium‐chain triglyceride consisting of three fatty acids with seven carbons each on a glycerol backbone, indicated for the treatment of adult and pediatric patients with long‐chain fatty acid oxidation disorders (LC‐FAOD). A total of 562 plasma concentrations of heptanoate, the most abundant and pharmacologically active metabolite of triheptanoin, from 13 healthy adult subjects and 30 adult and pediatric subjects with LC‐FAOD were included in the population pharmacokinetic (PK) analyses. Multiple peaks of heptanoate observed in several subjects were characterized by dual first‐order absorption with a lag time in the second absorption compartment. The disposition of heptanoate in human plasma was adequately described by one‐compartmental distribution with a linear elimination. The apparent clearance (CL/F) and apparent volume of distribution were allometrically scaled with body weight to describe PK data across a wide range of age groups in subjects with LC‐FAOD. The typical CL/F in adult subjects with LC‐FAOD was ≈19% lower than that in healthy subjects. Model‐estimated elimination half‐life for LC‐FAOD patients was ∼1.7 hours, supporting a recommended dosing frequency of ≥4 times per day. Covariate analyses indicate that age, race, and sex did not lead to clinically meaningful changes in the exposure of heptanoate. John Wiley and Sons Inc. 2022-07-31 2022-11 /pmc/articles/PMC9795984/ /pubmed/35908210 http://dx.doi.org/10.1002/cpdd.1145 Text en © 2022 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Lee, Sun Ku
Gosselin, Nathalie H.
Jomphe, Claudia
McKeever, Kathleen
Putnam, Wendy
Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title_full Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title_fullStr Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title_full_unstemmed Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title_short Population Pharmacokinetics of Heptanoate in Healthy Subjects and Patients With Long‐Chain Fatty Acid Oxidation Disorders Treated With Triheptanoin
title_sort population pharmacokinetics of heptanoate in healthy subjects and patients with long‐chain fatty acid oxidation disorders treated with triheptanoin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795984/
https://www.ncbi.nlm.nih.gov/pubmed/35908210
http://dx.doi.org/10.1002/cpdd.1145
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