• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

ABCG2 rs2231142 与别嘌醇及其代谢物浓度的关联研究。

An association study of ABCG2 rs2231142 on the concentrations of allopurinol and its metabolites.

机构信息

Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.

Montreal Heart Institute, Montreal, Quebec, Canada.

出版信息

Clin Transl Sci. 2022 Aug;15(8):2024-2034. doi: 10.1111/cts.13318. Epub 2022 Jun 10.

DOI:10.1111/cts.13318
PMID:35689378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9372422/
Abstract

ABCG2 is a gene that codes for the human breast cancer resistance protein (BCRP). It is established that rs2231142 G>T, a single nucleotide polymorphism of the ABCG2 gene, is associated with gout and poor response to allopurinol, a uric acid-lowering agent used to treat this condition. It has also been suggested that oxypurinol, the primary active metabolite of allopurinol, is a substrate of the BCRP. We thus hypothesized that carrying the rs2231142 variant would be associated with decreased oxypurinol concentrations, which would explain the lower reduction in uric acid. We performed a cross-sectional study to investigate the association between the ABCG2 rs2231142 variant and oxypurinol, allopurinol, and allopurinol riboside concentrations in 459 participants from the Montreal Heart Institute Hospital Cohort. Age, sex, weight, use of diuretics, and estimated glomerular filtration rate were all significantly associated with oxypurinol plasma concentration. No association was found between rs2231142 and oxypurinol, allopurinol and allopurinol riboside plasma concentrations. Rs2231142 was not significantly associated with daily allopurinol dose in the overall population, but an association was observed in men, with T carriers receiving higher doses. Our results do not support a major role of ABCG2 in the pharmacokinetics of allopurinol or its metabolites. The underlying mechanism of the association between rs2231142 and allopurinol efficacy requires further investigation.

摘要

ABCG2 是一种基因,编码人类乳腺癌耐药蛋白(BCRP)。现已确定,ABCG2 基因的单核苷酸多态性 rs2231142G>T 与痛风和别嘌醇(一种用于治疗该疾病的降低尿酸药物)反应不良有关。有人还提出,别嘌醇的主要活性代谢物氧嘌呤醇是 BCRP 的底物。因此,我们假设携带 rs2231142 变体与降低的氧嘌呤醇浓度有关,这可以解释尿酸降低减少的原因。我们进行了一项横断面研究,以调查 459 名来自蒙特利尔心脏研究所医院队列的参与者中 ABCG2 rs2231142 变体与氧嘌呤醇、别嘌醇和别嘌醇核苷浓度之间的关联。年龄、性别、体重、利尿剂的使用和估计的肾小球滤过率均与氧嘌呤醇血浆浓度显著相关。rs2231142 与氧嘌呤醇、别嘌醇和别嘌醇核苷血浆浓度之间没有关联。rs2231142 与整个人群中的别嘌醇日剂量无显著相关性,但在男性中存在相关性,T 携带者接受的剂量较高。我们的结果不支持 ABCG2 在别嘌醇或其代谢物的药代动力学中起主要作用。rs2231142 与别嘌醇疗效之间关联的潜在机制需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4b/9372422/3067c29c71b8/CTS-15-2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4b/9372422/3067c29c71b8/CTS-15-2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4b/9372422/3067c29c71b8/CTS-15-2024-g001.jpg

相似文献

1
An association study of ABCG2 rs2231142 on the concentrations of allopurinol and its metabolites.ABCG2 rs2231142 与别嘌醇及其代谢物浓度的关联研究。
Clin Transl Sci. 2022 Aug;15(8):2024-2034. doi: 10.1111/cts.13318. Epub 2022 Jun 10.
2
Investigation of the transport of xanthine dehydrogenase inhibitors by the urate transporter ABCG2.尿酸盐转运蛋白ABCG2对黄嘌呤脱氢酶抑制剂转运的研究。
Drug Metab Pharmacokinet. 2018 Feb;33(1):77-81. doi: 10.1016/j.dmpk.2017.11.002. Epub 2017 Nov 22.
3
Relationships Between Allopurinol Dose, Oxypurinol Concentration and Urate-Lowering Response-In Search of a Minimum Effective Oxypurinol Concentration.别嘌醇剂量、氧嘌呤醇浓度与降尿酸反应的关系——寻找最小有效氧嘌呤醇浓度。
Clin Transl Sci. 2020 Jan;13(1):110-115. doi: 10.1111/cts.12686. Epub 2019 Sep 3.
4
ABCG2 loss-of-function polymorphism predicts poor response to allopurinol in patients with gout.ABCG2功能缺失多态性预示痛风患者对别嘌醇反应不佳。
Pharmacogenomics J. 2017 Mar;17(2):201-203. doi: 10.1038/tpj.2015.101. Epub 2016 Jan 26.
5
Oxypurinol pharmacokinetics and pharmacodynamics in healthy volunteers: Influence of BCRP Q141K polymorphism and patient characteristics.健康志愿者中别嘌醇的药代动力学和药效学:BCRP Q141K 多态性和患者特征的影响。
Clin Transl Sci. 2021 Jul;14(4):1431-1443. doi: 10.1111/cts.12992. Epub 2021 May 1.
6
Association between ABCG2 rs2231142 and poor response to allopurinol: replication and meta-analysis.ABCG2 rs2231142 与别嘌醇反应不良的相关性:复制和荟萃分析。
Rheumatology (Oxford). 2018 Apr 1;57(4):656-660. doi: 10.1093/rheumatology/kex467.
7
ABCG2 gene polymorphism rs2231142 is associated with gout comorbidities but not allopurinol response in primary gout patients of a Chinese Han male population.ABCG2 基因多态性 rs2231142 与中国汉族男性原发性痛风患者的痛风合并症相关,但与别嘌醇反应无关。
Hereditas. 2019 Jul 24;156:26. doi: 10.1186/s41065-019-0103-y. eCollection 2019.
8
ABCG2 rs2231142 (Q141K) and oxypurinol concentrations in people with gout receiving allopurinol.接受别嘌醇治疗的痛风患者中ABCG2基因rs2231142(Q141K)与氧嘌呤醇浓度的关系
Drug Metab Pharmacokinet. 2018 Dec;33(6):241-242. doi: 10.1016/j.dmpk.2018.09.002. Epub 2018 Sep 18.
9
The effect of benzbromarone on allopurinol/oxypurinol kinetics in patients with gout.苯溴马隆对痛风患者别嘌醇/氧嘌呤醇动力学的影响。
Eur J Clin Pharmacol. 1993;44(1):69-72. doi: 10.1007/BF00315283.
10
Genome-Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.全基因组关联和功能研究揭示别嘌醇的新药理学机制。
Clin Pharmacol Ther. 2019 Sep;106(3):623-631. doi: 10.1002/cpt.1439. Epub 2019 May 23.

引用本文的文献

1
The genetics of gout: translation into clinical practice.痛风的遗传学:转化为临床实践
Ther Adv Musculoskelet Dis. 2025 Aug 25;17:1759720X251366360. doi: 10.1177/1759720X251366360. eCollection 2025.
2
A Study Of the effect of Sex on drug dosing, concentrations, and pharmacogenomics in the Montreal Heart Institute Hospital Cohort (SOS-PGx): methodology and research progress.蒙特利尔心脏研究所队列研究中性别对药物剂量、浓度和药物基因组学的影响(SOS-PGx):方法与研究进展
Eur J Clin Pharmacol. 2025 Feb;81(2):321-332. doi: 10.1007/s00228-024-03786-3. Epub 2024 Dec 20.
3
A systematic review of single nucleotide polymorphisms affecting allopurinol pharmacokinetics and serum uric acid level.

本文引用的文献

1
Leveraging large observational studies to discover genetic determinants of drug concentrations: A proof-of-concept study.利用大型观察性研究发现药物浓度的遗传决定因素:概念验证研究。
Clin Transl Sci. 2022 Apr;15(4):1063-1073. doi: 10.1111/cts.13230. Epub 2022 Feb 5.
2
Sex Differences in Urate Handling.尿酸处理中的性别差异。
Int J Mol Sci. 2020 Jun 16;21(12):4269. doi: 10.3390/ijms21124269.
3
The ABCG2 Q141K hyperuricemia and gout associated variant illuminates the physiology of human urate excretion.ABCG2 Q141K 致高尿酸血症和痛风相关变异体阐明了人类尿酸排泄的生理学。
一项影响别嘌醇药代动力学和血清尿酸水平的单核苷酸多态性的系统评价。
Pharmacogenomics. 2024;25(10-11):479-494. doi: 10.1080/14622416.2024.2403969. Epub 2024 Sep 30.
4
Association of rare and common genetic variants in MOCOS with inadequate response to allopurinol.MOCOS 中的罕见和常见遗传变异与别嘌醇反应不足的关联。
Rheumatology (Oxford). 2024 Nov 1;63(11):3025-3032. doi: 10.1093/rheumatology/keae420.
5
A Genome-Wide Association Study of Oxypurinol Concentrations in Patients Treated with Allopurinol.接受别嘌醇治疗患者的氧嘌呤醇浓度全基因组关联研究。
J Pers Med. 2024 Jun 18;14(6):649. doi: 10.3390/jpm14060649.
6
Impact of amiodarone use on metoprolol concentrations, α-OH-metoprolol concentrations, metoprolol dosing and heart rate: A cross-sectional study.胺碘酮使用对美托洛尔浓度、α-OH-美托洛尔浓度、美托洛尔剂量和心率的影响:一项横断面研究。
Pharmacol Res Perspect. 2023 Oct;11(5):e01137. doi: 10.1002/prp2.1137.
7
Population pharmacokinetics, pharmacodynamics and pharmacogenetics modelling of oxypurinol in Hmong adults with gout and/or hyperuricemia.黄嘌呤醇在患有痛风和/或高尿酸血症的苗族成年人中的群体药代动力学、药效学和药物遗传学建模。
Br J Clin Pharmacol. 2023 Oct;89(10):2964-2976. doi: 10.1111/bcp.15792. Epub 2023 Jun 4.
8
Cannabis Pharmacogenomics: A Path to Personalized Medicine.大麻药物基因组学:通往个性化医疗之路。
Curr Issues Mol Biol. 2023 Apr 17;45(4):3479-3514. doi: 10.3390/cimb45040228.
9
Females present higher dose-adjusted drug concentrations of metoprolol and allopurinol/oxypurinol than males.女性的美托洛尔和别嘌醇/氧嘌呤醇的剂量调整药物浓度高于男性。
Clin Transl Sci. 2023 May;16(5):872-885. doi: 10.1111/cts.13497. Epub 2023 Mar 2.
10
The impact of genetic variability in urate transporters on oxypurinol pharmacokinetics.尿酸转运体遗传变异对别嘌醇药代动力学的影响。
Clin Transl Sci. 2023 Mar;16(3):422-428. doi: 10.1111/cts.13460. Epub 2022 Nov 25.
Nat Commun. 2020 Jun 2;11(1):2767. doi: 10.1038/s41467-020-16525-w.
4
Relationships Between Allopurinol Dose, Oxypurinol Concentration and Urate-Lowering Response-In Search of a Minimum Effective Oxypurinol Concentration.别嘌醇剂量、氧嘌呤醇浓度与降尿酸反应的关系——寻找最小有效氧嘌呤醇浓度。
Clin Transl Sci. 2020 Jan;13(1):110-115. doi: 10.1111/cts.12686. Epub 2019 Sep 3.
5
Pharmacogenetics of statins treatment: Efficacy and safety.他汀类药物治疗的药物遗传学:疗效和安全性。
J Clin Pharm Ther. 2019 Dec;44(6):858-867. doi: 10.1111/jcpt.13025. Epub 2019 Aug 22.
6
The impact of liver transplant recipient and donor genetic variability on tacrolimus exposure and transplant outcome.肝移植受者和供者遗传变异性对他克莫司暴露和移植结局的影响。
Br J Clin Pharmacol. 2019 Sep;85(9):2170-2175. doi: 10.1111/bcp.14034. Epub 2019 Jul 24.
7
Interactions between serum urate-associated genetic variants and sex on gout risk: analysis of the UK Biobank.血清尿酸相关遗传变异与性别在痛风风险中的相互作用:英国生物库分析。
Arthritis Res Ther. 2019 Jan 9;21(1):13. doi: 10.1186/s13075-018-1787-5.
8
ABCG2 rs2231142 (Q141K) and oxypurinol concentrations in people with gout receiving allopurinol.接受别嘌醇治疗的痛风患者中ABCG2基因rs2231142(Q141K)与氧嘌呤醇浓度的关系
Drug Metab Pharmacokinet. 2018 Dec;33(6):241-242. doi: 10.1016/j.dmpk.2018.09.002. Epub 2018 Sep 18.
9
Investigation of the transport of xanthine dehydrogenase inhibitors by the urate transporter ABCG2.尿酸盐转运蛋白ABCG2对黄嘌呤脱氢酶抑制剂转运的研究。
Drug Metab Pharmacokinet. 2018 Feb;33(1):77-81. doi: 10.1016/j.dmpk.2017.11.002. Epub 2017 Nov 22.
10
Association between ABCG2 rs2231142 and poor response to allopurinol: replication and meta-analysis.ABCG2 rs2231142 与别嘌醇反应不良的相关性:复制和荟萃分析。
Rheumatology (Oxford). 2018 Apr 1;57(4):656-660. doi: 10.1093/rheumatology/kex467.