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Impact of Inflammation on Cytochromes P450 Activity in Pediatrics: A Systematic Review.
Lenoir, Camille; Rodieux, Frédérique; Desmeules, Jules A; Rollason, Victoria; Samer, Caroline F.
Afiliação
  • Lenoir C; Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care, and Emergency Medicine, University Hospital of Geneva (HUG), Rue Gabrielle-Perret-Gentil 4, 1211, Geneva 14, Switzerland.
  • Rodieux F; Institute of Pharmaceutical Sciences of Western Switzerland (ISPSO), University of Geneva, Geneva, Switzerland.
  • Desmeules JA; School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
  • Rollason V; Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care, and Emergency Medicine, University Hospital of Geneva (HUG), Rue Gabrielle-Perret-Gentil 4, 1211, Geneva 14, Switzerland.
  • Samer CF; Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care, and Emergency Medicine, University Hospital of Geneva (HUG), Rue Gabrielle-Perret-Gentil 4, 1211, Geneva 14, Switzerland.
Clin Pharmacokinet ; 60(12): 1537-1555, 2021 12.
Article em En | MEDLINE | ID: mdl-34462878
ABSTRACT
BACKGROUND AND

OBJECTIVE:

Cytochromes P450 (CYP) are the major enzymes involved in hepatic metabolism of drugs. Personalization of treatment in pediatrics is a major challenge, as it must not only take into account genetic, environmental, and physiological factors but also ontogeny. Published data in adults show that inflammation had an isoform-specific impact on CYP activities and we aimed to evaluate this impact in the pediatric population.

METHODS:

Articles listed in PubMed through 7 January, 2021 that studied the impact of inflammation on CYP activities in pediatrics were included in this systematic review. Sources of inflammation, victim drugs (CYP involved), effect of drug-disease interactions, number and age of subjects, and study design were extracted.

RESULTS:

Twenty-seven studies and case reports were included. The impact of inflammation on CYP activities appeared to be age dependent and isoform-specific, with some drug-disease interactions having significant pharmacokinetic and clinical impact. For example, midazolam clearance decreases by 70%, while immunosuppressant and theophylline concentrations increase three-fold and two-fold with intensive care unit admission and infection. Cytochrome P450 activity appears to return to baseline level when the disease is resolved.

CONCLUSIONS:

Studies that have assessed the impact of inflammation on CYP activity are lacking in pediatrics, yet it is a major factor to consider to improve drug efficacy or safety. The scarce current data show that the impact of inflammation is isoform and age dependent. An effort must be made to improve the understanding of the impact of inflammation on CYP activities in children to better individualize treatment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pediatria / Sistema Enzimático do Citocromo P-450 Tipo de estudo: Systematic_reviews Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pediatria / Sistema Enzimático do Citocromo P-450 Tipo de estudo: Systematic_reviews Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article