Longitudinal exposure of English primary care patients to pharmacogenomic drugs: An analysis to inform design of pre-emptive pharmacogenomic testing.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
12 2019
Historique:
received: 04 06 2019
revised: 02 08 2019
accepted: 09 08 2019
pubmed: 28 8 2019
medline: 29 9 2020
entrez: 28 8 2019
Statut: ppublish

Résumé

To investigate the longitudinal exposure of English primary care patients to pharmacogenomic drugs to inform design of pre-emptive testing. Sixty-three drugs were identified with dosing guidelines based on variants of 19 pharmacogenes in the Pharmacogenomics Knowledgebase on 01 September 2018. Prescribing of these pharmacogenomic drugs between 1993 and 2017 was summarised for a sample of 648 141 English patients aged 50-99 years on 01 January 2013, registered with Clinical Practice Research Datalink practices during 2011-12. Exposure of patients to pharmacogenomic drugs retrospectively (2, 10, 20 y) and prospectively (5 y) was described. During 2011-12, 58% of patients were prescribed at least 1 pharmacogenomic drug, increasing to 80% over the previous 20 years. Multiple exposure was common, with 47% patients prescribed ≥2 pharmacogenomic drugs and 7% prescribed ≥5 pharmacogenomic drugs over the next 5 years. The likelihood of exposure to pharmacogenomic drugs increased with age, with 89% patients ≥70 years prescribed at least 1 pharmacogenomic drug over the previous 20 years. Even among those aged 50-59 years, 71% were prescribed at least 1 pharmacogenomic drug over the previous 20 years. The pharmacogenomic drugs prescribed to the most patients were for pain relief, gastroprotection, psychiatric and cardiovascular conditions. Three pharmacogenes (CYP2D6, CYP2C19 and SLCO1B1) accounted for >95% pharmacogenomic drugs prescribed. In primary care patients, exposure to pharmacogenomic drugs is extremely common, multiplicitous and has commenced by relatively early adulthood. A small number of pharmacogenes account for the majority of drugs prescribed. These findings could inform design of pre-emptive pharmacogenomic testing for implementation in primary care.

Identifiants

pubmed: 31454087
doi: 10.1111/bcp.14100
pmc: PMC6955399
doi:

Substances chimiques

Liver-Specific Organic Anion Transporter 1 0
Pharmaceutical Preparations 0
SLCO1B1 protein, human 0
CYP2C19 protein, human EC 1.14.14.1
Cytochrome P-450 CYP2C19 EC 1.14.14.1
Cytochrome P-450 CYP2D6 EC 1.14.14.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2734-2746

Informations de copyright

© 2019 The British Pharmacological Society.

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Auteurs

James E Kimpton (JE)

Clinical Pharmacology, St George's University Hospitals NHS Foundation Trust, London, UK.
Institute of Medical and Biomedical Education, St George's, University of London, UK.

Iain M Carey (IM)

Population Health Research Institute, St George's, University of London, UK.

Christopher J D Threapleton (CJD)

Clinical Pharmacology, St George's University Hospitals NHS Foundation Trust, London, UK.
Institute of Medical and Biomedical Education, St George's, University of London, UK.

Alexandra Robinson (A)

Clinical Pharmacology, St George's University Hospitals NHS Foundation Trust, London, UK.

Tess Harris (T)

Population Health Research Institute, St George's, University of London, UK.
Sonning Common Health Centre, Sonning Common, Reading, UK.

Derek G Cook (DG)

Population Health Research Institute, St George's, University of London, UK.

Stephen DeWilde (S)

Population Health Research Institute, St George's, University of London, UK.
Lambton Road Medical Practice, Wimbledon, London, UK.

Emma H Baker (EH)

Clinical Pharmacology, St George's University Hospitals NHS Foundation Trust, London, UK.
Institute of Infection and Immunity, St George's, University of London, UK.

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Classifications MeSH