Publication:
Meta-Analysis of NUDT15 Genetic Polymorphism on Thiopurine-Induced Myelosuppression in Asian Populations

dc.contributor.authorKanyarat Khaesoen_US
dc.contributor.authorSariya Udayachalermen_US
dc.contributor.authorPatcharee Komvilaisaken_US
dc.contributor.authorSu On Chainansamiten_US
dc.contributor.authorKunanya Suwannayingen_US
dc.contributor.authorNapat Laoaroonen_US
dc.contributor.authorPitchayanan Kuwatjanakulen_US
dc.contributor.authorNontaya Nakkamen_US
dc.contributor.authorChonlaphat Sukasemen_US
dc.contributor.authorApichaya Puangpetchen_US
dc.contributor.authorWichittra Tassaneeyakulen_US
dc.contributor.authorNathorn Chaiyakunapruken_US
dc.contributor.otherRamathibodi Hospitalen_US
dc.contributor.otherUdon Thani Center Hospitalen_US
dc.contributor.otherFaculty of Medicine, Khon Kaen Universityen_US
dc.contributor.otherFaculty of Medicine Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherKhon Kaen Regional Hospitalen_US
dc.contributor.otherUniversity of Utah Healthen_US
dc.date.accessioned2022-08-04T08:58:11Z
dc.date.available2022-08-04T08:58:11Z
dc.date.issued2021-12-02en_US
dc.description.abstractBackgound: The high incidence of thiopurine-induced myelosuppression in Asians is known to be attributable to genetic variation in thiopurine metabolism. A quantitative synthesis to summarize the genetic association with thiopurine-induced myelosuppression in Asians was therefore conducted. Methods: A Literature search was performed from January 2016 to May 2021 in the following databases: PubMed, Web of Science, and Embase and addition search included the studies from Zhang et al. Two reviewers independently extracted the following data: the author’s name, year of publication, ethnicity, drugs, diseases, genetic polymorphisms, onset, type of myelosuppression and results of Hardy-Weinberg equilibrium. The Newcastle-Ottawa Scale was used to assess the quality of the studies. The pooled odds ratios (OR) and 95% confidence intervals (CI) were calculated to evaluate the associations of NUDT15 and the risk of thiopurine-induced myelosuppression stratified by onset and type of myelosuppressive. Subgroup analysis by NUDT15 genetic polymorphisms was performed. Results: A total of 30 studies was included in this meta-analysis. The overall OR for the relationship between NUDT15 genetic polymorphisms and thiopurine-induced early onset of leukopenia and neutropenia in Asian populations were 11.43 (95% CI 7.11–18.35) and 16.35 (95% CI 10.20–26.22). Among NUDT15 polymorphisms, NUDT15*3 showed a significantly increased risk of early leukopenia (OR 15.31; 95% CI 9.65–24.27) and early neutropenia (OR 15.85; 95% CI 8.80–28.53). A significantly higher thiopurine-induced early neutropenic risk was also found for NUDT15*2 (OR 37.51; 95% CI 1.99–708.69). Whereas, NUDT15*5 and NUDT15*6 variants showed a lower risk of leukopenia. Conclusion: This study suggests that NUDT15*3 and NUDT15*2 are important genetic markers of thiopurine-induced early onset of myelotoxicity in Asians, therefore, early detection of these variants before initiating thiopurine therapy is necessary.en_US
dc.identifier.citationFrontiers in Pharmacology. Vol.12, (2021)en_US
dc.identifier.doi10.3389/fphar.2021.784712en_US
dc.identifier.issn16639812en_US
dc.identifier.other2-s2.0-85121455340en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/77411
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85121455340&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleMeta-Analysis of NUDT15 Genetic Polymorphism on Thiopurine-Induced Myelosuppression in Asian Populationsen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85121455340&origin=inwarden_US

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