Literature DB >> 22676193

UGT2B7 genetic polymorphisms are associated with the withdrawal symptoms in methadone maintenance patients.

Jia-Ni Tian1, Ing-Kang Ho, Hsiao-Hui Tsou, Chiu-Ping Fang, Chin-Fu Hsiao, Chia-Hui Chen, Happy Kuy-Lok Tan, Linen Lin, Chi-Shin Wu, Lien-Wen Su, Chieh-Liang Huang, Yi-Hong Yang, Ming-Lun Liu, Yu-Ting Chen, Shu Chih Liu, Ya-Ting Hsu, Hsiang-Wei Kuo, Chen Ting Liu, Yi-Ting Yang, Andrew Ch Chen, Yu-Huei Shih, Yu-Li Liu.   

Abstract

AIM: To test whether the genetic polymorphisms within the gene encoding the UGT2B7 gene may have an impact on methadone treatment. MATERIALS &
METHODS: Twelve SNPs in UGT2B7 were selected. 366 methadone maintenance treatment patients in Taiwan were recruited and genotyped.
RESULTS: In a genotype recessive model, rs6600879, rs6600880, rs4554144, rs11940316, rs7438135, rs7662029, rs7668258, rs7439366, rs4292394 and rs6600893 showed significant associations with severity of withdrawal symptoms (permutation p < 0.002), pupil size (permutation p < 0.048) and tremor (permutation p < 0.008). Haplotypes of GATCAGCCGC and CTCTGATTCT were significantly associated with pupil size score and tremor score (p < 0.034).
CONCLUSION: These results suggest that SNPs of the UGT2B7 gene may play important roles in opiate withdrawal symptoms.

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Year:  2012        PMID: 22676193     DOI: 10.2217/pgs.12.69

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


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