A systematic review of single nucleotide polymorphisms affecting allopurinol pharmacokinetics and serum uric acid level

被引：0
|
作者：
Azwan, Farah Aida A. Zairol [1 ]
Ying, Teo Yi [1 ]
Tahir, Nor Asyikin Mohd [1 ]
Saffian, Shamin Mohd [1 ]
Makmor-Bakry, Mohd [1 ,2 ]
Said, Mohd Shahrir Mohamed [3 ]
机构：
[1] Univ Kebangsaan Malaysia, Fac Pharm, Ctr Qual Management Med, Jalan Raja Muda Abdul Aziz, Kuala Lumpur 50300, Malaysia
[2] Univ Airlangga, Fac Pharm, PQMM9Q6,Gedung Nanizar Zaman Joenoes Kampus C UNAI, Surabaya 60115, E Java, Indonesia
[3] Univ Kebangsaan Malaysia, Hosp Canselor Tuanku Muhriz, Dept Med, Jalan Yaacob Latiff, Kuala Lumpur 56000, Malaysia
来源：
PHARMACOGENOMICS | 2024年 / 25卷 / 10-11期
关键词：
allopurinol; clearance; oxypurinol; pharmacokinetics; single nucleotide polymorphisms; SNPs; uric acid level; GENOME-WIDE ASSOCIATION; POOR RESPONSE; GOUT; DISEASE; IMPACT; EPIDEMIOLOGY; TRANSPORTER; INHIBITORS; OXYPURINOL; URATE;
D O I：
10.1080/14622416.2024.2403969
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
Aim: To summarize the effects of single nucleotide polymorphisms (SNPs) on the pharmacokinetics of allopurinol to control uric acid levels. Methods: A comprehensive search was conducted in PubMed, Web of Science and Scopus databases from inception to January 2024, includes 17 articles focusing on SNPs and pharmacokinetics of allopurinol and oxypurinol. Results: A total of 11 SNPs showed a significant association with pharmacokinetics of allopurinol and oxypurinol, as well as their potential clinical implications. Conclusion: SNPs in ATP-binding cassette super-family G member 2 (ABCG2), solute carrier family 2 member 9 (SLC2A9), solute carrier family 17 member 1 (SLC17A1), solute carrier family 22 member 12 (SLC22A12), solute carrier family 22 member 13 (SLC22A13) and PDZ domain containing 1 (PDZK1) genes were associated with allopurinol clearance, while SNPs in aldehyde oxidase 1 (AOX1) genes involved in metabolism of allopurinol. SNPs in gremlin 2, DAN family BMP antagonist (GREM2) gene impacted uric acid control, but the specific mechanism governing the expression of GREM2 remains unknown. Our study indicated that the identified SNPs show contradictory effects, reflecting inconsistencies and differences observed across various studies.
引用
收藏
页码：479 / 494
页数：16
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