Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia

Abstract Background Nicotine metabolism significantly influences the levels of harmful nicotine metabolites in smokers. CYP2A13, a key enzyme in nicotine and xenobiotic metabolism, is implicated in tobacco smoke-related lung cancer. Aim This study investigated the association between CYP2A13 genetic...

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Main Authors: Noni Novisari Soeroso, Rozaimah Zain-Hamid, Syamsul Bihar, Chaliza Soliha, Fannie Rizki Ananda, Aida
Format: Article
Language:English
Published: SpringerOpen 2025-02-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Online Access:https://doi.org/10.1186/s43042-025-00653-3
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author Noni Novisari Soeroso
Rozaimah Zain-Hamid
Syamsul Bihar
Chaliza Soliha
Fannie Rizki Ananda
Aida
author_facet Noni Novisari Soeroso
Rozaimah Zain-Hamid
Syamsul Bihar
Chaliza Soliha
Fannie Rizki Ananda
Aida
author_sort Noni Novisari Soeroso
collection DOAJ
description Abstract Background Nicotine metabolism significantly influences the levels of harmful nicotine metabolites in smokers. CYP2A13, a key enzyme in nicotine and xenobiotic metabolism, is implicated in tobacco smoke-related lung cancer. Aim This study investigated the association between CYP2A13 genetic polymorphism and nicotine metabolism in male smokers in Medan, Indonesia. Materials and methods This cross-sectional study included 66 male smokers (aged 20–65 years) who met pre-defined inclusion and exclusion criteria. Nicotine metabolite levels were quantified in urine samples using high-performance liquid chromatography (HPLC). CYP2A13 polymorphism was determined using polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) analysis of venous blood samples. Logistic regression analysis (Epi Info-7) assessed the association between CYP2A13 genotype and nicotine metabolism. Results No significant association (p > 0.05) was found between CYP2A13 genotype and nicotine metabolism. The CC genotype was most prevalent. The majority of participants exhibited rapid nicotine metabolism. Conclusion Further research with larger sample sizes and diverse populations is needed to elucidate the relationship between CYP2A13 genetic polymorphism and nicotine metabolism.
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institution Kabale University
issn 2090-2441
language English
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publisher SpringerOpen
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series Egyptian Journal of Medical Human Genetics
spelling doaj-art-4653f7c639bc45ee81ad495487fc98202025-02-09T12:40:10ZengSpringerOpenEgyptian Journal of Medical Human Genetics2090-24412025-02-012611710.1186/s43042-025-00653-3Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, IndonesiaNoni Novisari Soeroso0Rozaimah Zain-Hamid1Syamsul Bihar2Chaliza Soliha3Fannie Rizki Ananda4Aida5Thoracic Oncology Division, Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera UtaraDepartment of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Sumatera UtaraDepartment of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera UtaraDepartment of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera UtaraDepartment of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera UtaraDepartment of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera UtaraAbstract Background Nicotine metabolism significantly influences the levels of harmful nicotine metabolites in smokers. CYP2A13, a key enzyme in nicotine and xenobiotic metabolism, is implicated in tobacco smoke-related lung cancer. Aim This study investigated the association between CYP2A13 genetic polymorphism and nicotine metabolism in male smokers in Medan, Indonesia. Materials and methods This cross-sectional study included 66 male smokers (aged 20–65 years) who met pre-defined inclusion and exclusion criteria. Nicotine metabolite levels were quantified in urine samples using high-performance liquid chromatography (HPLC). CYP2A13 polymorphism was determined using polymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) analysis of venous blood samples. Logistic regression analysis (Epi Info-7) assessed the association between CYP2A13 genotype and nicotine metabolism. Results No significant association (p > 0.05) was found between CYP2A13 genotype and nicotine metabolism. The CC genotype was most prevalent. The majority of participants exhibited rapid nicotine metabolism. Conclusion Further research with larger sample sizes and diverse populations is needed to elucidate the relationship between CYP2A13 genetic polymorphism and nicotine metabolism.https://doi.org/10.1186/s43042-025-00653-3CYP2A13 polymorphismMale smokersNicotine metabolismNicotine metabolite ratioIndonesia
spellingShingle Noni Novisari Soeroso
Rozaimah Zain-Hamid
Syamsul Bihar
Chaliza Soliha
Fannie Rizki Ananda
Aida
Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
Egyptian Journal of Medical Human Genetics
CYP2A13 polymorphism
Male smokers
Nicotine metabolism
Nicotine metabolite ratio
Indonesia
title Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
title_full Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
title_fullStr Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
title_full_unstemmed Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
title_short Unraveling relationship between the genetic polymorphism CYP2A13 and nicotine metabolism of male smokers in Medan, Indonesia
title_sort unraveling relationship between the genetic polymorphism cyp2a13 and nicotine metabolism of male smokers in medan indonesia
topic CYP2A13 polymorphism
Male smokers
Nicotine metabolism
Nicotine metabolite ratio
Indonesia
url https://doi.org/10.1186/s43042-025-00653-3
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