Paola Nicoletti
Genetic Risk Factors in Drug‐Induced Liver Injury Due to Isoniazid‐Containing Antituberculosis Drug Regimens
Nicoletti, Paola; Devarbhavi, Harshad; Goel, Ashish; Venkatesan, Radha; Eapen, Chundamannil E.; Grove, Jane I.; Zafer, Samreen; Bjornsson, Einar; Lucena, M. Isabel; Andrade, Raul J.; Pirmohamed, Munir; Wadelius, Mia; Larrey, Dominique; Maitland-van der Zee, Anke-Hilse; Ibanez, Luisa; Watkins, Paul B.; Daly, Ann K.; Aithal, Guruprasad P.
Authors
Harshad Devarbhavi
Ashish Goel
Radha Venkatesan
Chundamannil E. Eapen
JANE GROVE jane.grove@nottingham.ac.uk
Associate Professor
Samreen Zafer
Einar Bjornsson
M. Isabel Lucena
Raul J. Andrade
Munir Pirmohamed
Mia Wadelius
Dominique Larrey
Anke-Hilse Maitland-van der Zee
Luisa Ibanez
Paul B. Watkins
Ann K. Daly
GURUPRASAD AITHAL Guru.Aithal@nottingham.ac.uk
Professor of Hepatology
Abstract
Drug‐induced liver injury (DILI) is a complication of treatment with anti‐tuberculosis (TB) drugs, especially in isoniazid‐containing regimens. To investigate genetic risk factors, we performed a genome‐wide association study (GWAS) involving anti‐TB DILI cases (55 Indian, 70 European) and controls (1199 Indian, 10397 European). Most cases were treated with a standard anti‐TB drug regimen; all received isoniazid. We imputed single nucleotide polymorphism and HLA genotypes and performed trans‐ethnic meta‐analysis on GWAS and candidate gene genotypes. GWAS found one significant association (rs117491755) in Europeans only. For HLA, HLA‐B*52:01 was significant (meta‐analysis odds ratio (OR) 2.67; 95%CI 1.63‐4.37; P=9.4x10‐5). For N‐acetyltransferase 2 (NAT2), NAT2*5 frequency was lower in cases (OR 0.69; 95%CI 0.57‐0.83, P=0.01). NAT2*6 and NAT2*7 were more common, with homozygotes for NAT2*6 and/or NAT2*7 enriched among cases (OR 1.89; 95%CI 0.84‐4.22; P=0.004). We conclude HLA genotype makes a small contribution to TB drug‐related DILI and that the NAT2 contribution is complex, but consistent with previous reports when differences in the metabolic effect of NAT2*5 compared with those of NAT2*6 and NAT2*7 are considered.
Citation
Nicoletti, P., Devarbhavi, H., Goel, A., Venkatesan, R., Eapen, C. E., Grove, J. I., …Aithal, G. P. (2021). Genetic Risk Factors in Drug‐Induced Liver Injury Due to Isoniazid‐Containing Antituberculosis Drug Regimens. Clinical Pharmacology and Therapeutics, 109(4), 1125-1135. https://doi.org/10.1002/cpt.2100
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 15, 2020 |
Online Publication Date | Dec 5, 2020 |
Publication Date | 2021-04 |
Deposit Date | Oct 22, 2020 |
Publicly Available Date | Dec 6, 2021 |
Journal | Clinical Pharmacology & Therapeutics |
Print ISSN | 0009-9236 |
Electronic ISSN | 1532-6535 |
Publisher | American Society for Clinical Pharmacology and Therapeutics |
Peer Reviewed | Peer Reviewed |
Volume | 109 |
Issue | 4 |
Pages | 1125-1135 |
DOI | https://doi.org/10.1002/cpt.2100 |
Keywords | drug-induced liver injury, HLA genes, adverse drug reactions, genetic polymorphisms, N-acetyltransferase 2, isoniazid |
Public URL | https://nottingham-repository.worktribe.com/output/4983499 |
Publisher URL | https://ascpt.onlinelibrary.wiley.com/doi/10.1002/cpt.2100 |
Additional Information | Received: 2020-07-20; Accepted: 2020-10-15; Published: 2020-12-05 |
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