Association of Drug Metabolic Enzyme Genetic Polymorphisms and Adverse Drug Reactions in Patients Receiving Rifapentine and Isoniazid Therapy for Latent Tuberculosis.


Journal

International journal of environmental research and public health
ISSN: 1660-4601
Titre abrégé: Int J Environ Res Public Health
Pays: Switzerland
ID NLM: 101238455

Informations de publication

Date de publication:
27 12 2019
Historique:
received: 11 11 2019
revised: 24 12 2019
accepted: 25 12 2019
entrez: 2 1 2020
pubmed: 2 1 2020
medline: 9 6 2020
Statut: epublish

Résumé

Weekly rifapentine and isoniazid therapy (3HP) is the most frequent treatment for latent tuberculosis infection (LTBI). However, the association between major adverse drug reactions (ADRs) and drug metabolic enzyme single-nucleotide polymorphisms (SNPs) remains unclear. In this study, 377 participants who received the 3HP regimen were recruited and examined for genotyping of CYP5A6, CYP2B6, CYP2C19, CYP2E1, and NAT2 SNPs. In our study, 184 participants (48.4%) developed ADRs. Moreover, CYP2C19 rs4986893 (TT vs. CC+CT, odds ratio [OR] [95% CI]: 2.231 [1.015-4.906]), CYP2E1 rs2070676 (CC vs. CG+GG, OR [95% CI]: 1.563 [1.022-2.389]), and CYP2E1 rs2515641 (CC vs. CT+TT, OR [95% CI]: 1.903 [1.250-2.898]) were associated with ADR development. In conclusion, CYP2C19 and CYP2E1 SNPs may provide useful information regarding ADRs in LTBI patients receiving the 3HP regimen.

Identifiants

pubmed: 31892222
pii: ijerph17010210
doi: 10.3390/ijerph17010210
pmc: PMC6981901
pii:
doi:

Substances chimiques

Antitubercular Agents 0
Cytochrome P-450 Enzyme System 9035-51-2
Arylamine N-Acetyltransferase EC 2.3.1.5
NAT2 protein, human EC 2.3.1.5
Isoniazid V83O1VOZ8L
Rifampin VJT6J7R4TR
rifapentine XJM390A33U

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Ya-Yen Yu (YY)

Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Department of Clinical Laboratory, Changhua Hospital, Changhua 513, Taiwan.

Shih-Ming Tsao (SM)

Division of Chest, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung 402, Taiwan.
Institute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung 402, Taiwan.

Wen-Ta Yang (WT)

Department of Internal Medicine, Taichung Hospital, Ministry of Health and Welfare, Taichung 403, Taiwan.

Wei-Chang Huang (WC)

Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan.
Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli 356, Taiwan.
Department of Life Sciences, National Chung Hsing University, Taichung 402, Taiwan.
Department of Industrial Engineering and Enterprise Information, Tunghai University, Taichung 407, Taiwan.

Ching-Hsiung Lin (CH)

Division of Chest, Changhua Christian Hospital, Changhua 500, Taiwan.

Wei-Wen Chen (WW)

Department of Health, Pulmonary and Critical Care Unit, Changhua Hospital, Changhua 500, Taiwan.

Shun-Fa Yang (SF)

Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Department of Medical Research, Chung Shan Medical University Hospital, Taichung 402, Taiwan.

Hui-Ling Chiou (HL)

School of Medical Laboratory and Biotechnology, Chung Shan Medical University, Taichung 402, Taiwan.
Department of Clinical Laboratory, Chung Shan Medical University Hospital, Taichung 402, Taiwan.

Yi-Wen Huang (YW)

Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Department of Health, Pulmonary and Critical Care Unit, Changhua Hospital, Changhua 500, Taiwan.

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Classifications MeSH