Please use this identifier to cite or link to this item:
https://doi.org/10.2217/pgs.12.24
DC Field | Value | |
---|---|---|
dc.title | CYP2C19 and PON1 polymorphisms regulating clopidogrel bioactivation in Chinese, Malay and Indian subjects | |
dc.contributor.author | Chan, M.Y. | |
dc.contributor.author | Tan, K. | |
dc.contributor.author | Tan, H.-C. | |
dc.contributor.author | Huan, P.-T. | |
dc.contributor.author | Li, B. | |
dc.contributor.author | Phua, Q.-H. | |
dc.contributor.author | Lee, H.-K. | |
dc.contributor.author | Lee, C.-H. | |
dc.contributor.author | Low, A. | |
dc.contributor.author | Becker, R.C. | |
dc.contributor.author | Ong, W.-C. | |
dc.contributor.author | Richards, M.A. | |
dc.contributor.author | Salim, A. | |
dc.contributor.author | Tai, E.-S. | |
dc.contributor.author | Koay, E. | |
dc.date.accessioned | 2014-11-26T05:02:42Z | |
dc.date.available | 2014-11-26T05:02:42Z | |
dc.date.issued | 2012-04 | |
dc.identifier.citation | Chan, M.Y., Tan, K., Tan, H.-C., Huan, P.-T., Li, B., Phua, Q.-H., Lee, H.-K., Lee, C.-H., Low, A., Becker, R.C., Ong, W.-C., Richards, M.A., Salim, A., Tai, E.-S., Koay, E. (2012-04). CYP2C19 and PON1 polymorphisms regulating clopidogrel bioactivation in Chinese, Malay and Indian subjects. Pharmacogenomics 13 (5) : 533-542. ScholarBank@NUS Repository. https://doi.org/10.2217/pgs.12.24 | |
dc.identifier.issn | 14622416 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/108902 | |
dc.description.abstract | Aim, materials & methods: We investigated the functional significance of CYP2C19*2, *3, *17 and PON1 Q192R SNPs in 89 consecutive Asian patients on clopidogrel treatment and the prevalence of functionally significant polymorphisms among 300 Chinese, Malays and Asian Indians. Results: Both CYP2C19 loss-of-function alleles (*2 or *3) were associated with higher platelet reactivity while the CYP2C19 gain-of-function allele (*17) had lower platelet reactivity. For PON1, the median PRI was not significantly different between the QQ, QR and RR groups. The allele frequencies of CYP2C19*2, CYP2C19*3 and CYP2C19*17 were 0.280, 0.065 and 0.010 (rare) for Chinese, 0.310, 0.050 and 0.025 for Malays, and 0.375, 0.010 (rare) and 0.165 for Indians, respectively. Conclusion: Our data suggest that genotyping studies to investigate clopidogrel response should include CYP2C19*2 and *3 but not *17 polymorphisms in Chinese, and CYP2C19*2 and *17 polymorphisms but not *3 in Indians. All three polymorphisms should preferably be genotyped in Malays. Original submitted 16 December 2011; Revision submitted 16 February 201. © 2012 Future Medicine Ltd. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.2217/pgs.12.24 | |
dc.source | Scopus | |
dc.subject | Asian | |
dc.subject | clopidogrel | |
dc.subject | CYP2C19 | |
dc.subject | metabolism | |
dc.subject | pharmacogenetics | |
dc.subject | PON1 | |
dc.type | Article | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.description.doi | 10.2217/pgs.12.24 | |
dc.description.sourcetitle | Pharmacogenomics | |
dc.description.volume | 13 | |
dc.description.issue | 5 | |
dc.description.page | 533-542 | |
dc.description.coden | PARMF | |
dc.identifier.isiut | 000302331400012 | |
Appears in Collections: | Staff Publications |
Show simple item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.