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Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisation

  • Charlotte King
  • , Amanda McKenna
  • , Niloufar Farzan
  • , Susanne J. Vijverberg
  • , Marc P. van der Schee
  • , Anke H. Maitland-van der Zee
  • , Lambang Arianto
  • , Hans Bisgaard
  • , Klaus BØnnelykke
  • , Vojko Berce
  • , Uroš Potočnik
  • , Katja Repnik
  • , Bruce Carleton
  • , Denise Daley
  • , Fook Tim Chew
  • , Wen Chin Chiang
  • , Yang Yie Sio
  • , Michelle M. Cloutier
  • , Herman T. Den Dekker
  • , Liesbeth Duijts
  • Johan C. de Jongste, F. Nicole Dijk, Gerard H. Koppelman, Carlos Flores, Natalia Hernandez-Pacheco, Maria Pino-Yanes, Somnath Mukhopadhyay, Kaninika Basu, Lauren Bignell, Kelan G. Tantisira, Steve Turner, Katia M. Verhamme, Ben Francis, Munir Pirmohamed, Ian Sinha, Daniel B. Hawcutt* (Corresponding Author)
*Corresponding author for this work
  • University of Amsterdam
  • University Medical Centre Maribor
  • University of Maribor
  • University of British Columbia
  • National University of Singapore
  • KK Children’s Hospital
  • University of Connecticut
  • Erasmus University Rotterdam
  • University of Groningen
  • Hospital Universitario Nuestra Senora de Candelaria
  • Brighton and Sussex Medical School
  • Harvard University
  • Alder Hey Children's NHS Foundation Trust
  • University of Liverpool
  • University of Copenhagen

Research output: Contribution to journalReview articlepeer-review

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Abstract

A systematic review of pharmacogenomic studies capturing adverse drug reactions (ADRs) related to asthma medications was undertaken, and a survey of Pharmacogenomics in Childhood Asthma (PiCA) consortia members was conducted. Studies were eligible if genetic polymorphisms were compared with suspected ADR(s) in a patient with asthma, as either a primary or secondary outcome. Five studies met the inclusion criteria. The ADRs and polymorphisms identified were change in lung function tests (rs1042713), adrenal suppression (rs591118), and decreased bone mineral density (rs6461639) and accretion (rs9896933, rs2074439). Two of these polymorphisms were replicated within the paper, but none had external replication. Priorities from PiCA consortia members (representing 15 institution in eight countries) for future studies were tachycardia (SABA/LABA), adrenal suppression/crisis and growth suppression (corticosteroids), sleep/behaviour disturbances (leukotriene receptor antagonists), and nausea and vomiting (theophylline). Future pharmacogenomic studies in asthma should collect relevant ADR data as well as markers of efficacy.

Original languageEnglish
Pages (from-to)621-628
Number of pages8
JournalPharmacogenomics Journal
Volume20
Early online date17 Jan 2020
DOIs
Publication statusPublished - Oct 2020

Bibliographical note

We would like to thank the NIHR Collaboration for Leadership in Applied Health Research and Care North West Coast (CLAHRC) for funding Amanda McKenna’s internship, and Charlotte Kings MPhil, and the members of the PiCA consortia for their help in completing the survey. U. Potočnik, K. Repnik and V. Berce were supported by SysPharmPedia grant, co-financed by Ministry of Education, Science and Sport of the Republic of Slovenia

Author information
These authors contributed equally: Charlotte King, Amanda McKenna
These authors jointly supervised this work: Ian Sinha, Daniel B. Hawcutt

Funding

Acknowledgements We would like to thank the NIHR Collaboration for Leadership in Applied Health Research and Care North West Coast (CLAHRC) for funding Amanda McKenna’s internship, and Charlotte Kings MPhil, and the members of the PiCA consortia for their help in completing the survey. U. Potočnik, K. Repnik and V. Berce were supported by SysPharmPedia grant, co-financed by Ministry of Education, Science and Sport of the Republic of Slovenia

Keywords

  • CHILDREN
  • EXACERBATIONS
  • RISK
  • POLYMORPHISM
  • BURDEN

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