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中国中部地区药物遗传学检测的临床应用现状:一项单中心研究

The Landscape of Clinical Implementation of Pharmacogenetic Testing in Central China: A Single-Center Study.

作者信息

Zhang Jingmin, Qi Guangzhao, Han Chao, Zhou Yubing, Yang Yongjie, Wang Xinru, Liu Suna, Zhang Xiaojian

机构信息

Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

Henan Key Laboratory for Precision Clinical Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

出版信息

Pharmgenomics Pers Med. 2021 Dec 14;14:1619-1628. doi: 10.2147/PGPM.S338198. eCollection 2021.

DOI:10.2147/PGPM.S338198
PMID:34934339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8684419/
Abstract

PURPOSE

Pharmacogenetic testing is recognized as the major method for the individualized pharmacotherapy in clinical pharmacy practice, but information about the clinical implementation of pharmacogenetic testing in China is limited. The present study aimed to determine the situation of clinical implementation for pharmacogenetic testing in central China.

METHODS

The study is conducted in the department of clinical pharmacy in The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. We collected and analyzed pharmacogenetic testing results from November 1, 2013 to November 2, 2018 in our hospital, which were checked in the electronic medical record system. The main outcome measures were the number and type of pharmacogenetic testing across five years.

RESULTS

A total of 47,265 (56.9% male, mean age = 51.5 years) pharmacogenetic testing results were obtained with an average annual rate of growth of 63.0% across five years. A 50.2% (23,748/47,265) of all the pharmacogenetic testing results were for the determination of cytochrome P450 2C19 () *2, *3 genotypes, and 41.7% were for the methylene tetrahydrofolate reductase () C677T genotype. The number of departments performing the pharmacogenetic testing was 35, 63, 55, 52, 52 and 39 for 2013-2018, respectively, and the main top five departments were cardiology, psychiatry, ICU, cardiac surgery and intervention.

CONCLUSION

Clinical implementation of pharmacogenetic testing in China is growing rapidly, but the types and implementing departments of pharmacogenetic testing were limited. Our present study reported the real-world implementation modality of pharmacogenomic tests in China. It will help us to understand the testing of pharmacogenetics in China in order to promote the rational development of pharmacogenetics.

摘要

目的

药物遗传学检测被认为是临床药学实践中个体化药物治疗的主要方法,但中国关于药物遗传学检测临床应用的信息有限。本研究旨在确定中国中部地区药物遗传学检测的临床应用情况。

方法

本研究在郑州大学第一附属医院临床药学部开展。我们收集并分析了2013年11月1日至2018年11月2日期间本院电子病历系统中记录的药物遗传学检测结果。主要观察指标为五年间药物遗传学检测的数量和类型。

结果

共获得47265份药物遗传学检测结果(男性占56.9%,平均年龄51.5岁),五年间平均年增长率为63.0%。所有药物遗传学检测结果中,50.2%(23748/47265)用于检测细胞色素P450 2C19()*2、*3基因型,41.7%用于检测亚甲基四氢叶酸还原酶()C677T基因型。2013 - 2018年进行药物遗传学检测的科室数量分别为35、63、55、52、52和39个,主要的前五个科室为心内科、精神科、重症监护室、心脏外科和介入科。

结论

中国药物遗传学检测的临床应用正在迅速增长,但药物遗传学检测的类型和实施科室有限。本研究报告了中国药物基因组学检测的真实世界应用模式。这将有助于我们了解中国药物遗传学检测情况,以促进药物遗传学的合理发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/75e5c83f0119/PGPM-14-1619-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/4bdd09ea82a0/PGPM-14-1619-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/a3b1ecb4cfbc/PGPM-14-1619-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/9cd846b18d71/PGPM-14-1619-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/75e5c83f0119/PGPM-14-1619-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/4bdd09ea82a0/PGPM-14-1619-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/a3b1ecb4cfbc/PGPM-14-1619-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/9cd846b18d71/PGPM-14-1619-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf09/8684419/75e5c83f0119/PGPM-14-1619-g0004.jpg

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本文引用的文献

1
Immune Checkpoint Molecules-Inherited Variations as Markers for Cancer Risk.免疫检查点分子——遗传变异作为癌症风险的标志物。
Front Immunol. 2021 Jan 14;11:606721. doi: 10.3389/fimmu.2020.606721. eCollection 2020.
2
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing.临床药物基因组学实施联盟(CPIC)CYP2C19 和质子泵抑制剂剂量指南。
Clin Pharmacol Ther. 2021 Jun;109(6):1417-1423. doi: 10.1002/cpt.2015. Epub 2020 Sep 20.
3
Pharmacogenomics and Personalized Medicine.药物基因组学与个性化医学。
在初级保健环境中实施药物基因组学检测的促成因素和挑战的范围综述。
BMJ Open. 2024 Nov 5;14(11):e087064. doi: 10.1136/bmjopen-2024-087064.
4
Advancing pharmacogenetic testing in a tertiary hospital: a retrospective analysis after 10 years of activity.三级医院推进药物遗传学检测:10年活动后的回顾性分析
Front Pharmacol. 2023 Oct 19;14:1292416. doi: 10.3389/fphar.2023.1292416. eCollection 2023.
5
Assessing pharmacogenomic literacy in China through validation of the Chinese version of the Minnesota Assessment of Pharmacogenomic Literacy.通过验证中文版明尼苏达州药物基因组学素养评估量表来评估中国的药物基因组学素养。
Clin Transl Sci. 2023 Nov;16(11):2356-2368. doi: 10.1111/cts.13637. Epub 2023 Oct 6.
6
A national survey of individualized pharmaceutical care practice in Chinese hospitals in 2019.2019年中国医院个体化药学服务实践的全国性调查。
Front Pharmacol. 2023 Mar 2;14:1022134. doi: 10.3389/fphar.2023.1022134. eCollection 2023.
Genes (Basel). 2020 Jun 22;11(6):679. doi: 10.3390/genes11060679.
4
Role of Genetic Variations in the Hepatic Handling of Drugs.遗传变异在药物肝脏处理中的作用。
Int J Mol Sci. 2020 Apr 20;21(8):2884. doi: 10.3390/ijms21082884.
5
Frequency and clinical outcomes of CYP2C19 genotype-guided escalation and de-escalation of antiplatelet therapy in a real-world clinical setting.在真实临床环境中,基于 CYP2C19 基因型指导的抗血小板治疗升阶和降阶的频率和临床结局。
Genet Med. 2020 Jan;22(1):160-169. doi: 10.1038/s41436-019-0611-1. Epub 2019 Jul 18.
6
Polymorphisms of methalenetetrahydrofolate reductase in recurrent pregnancy loss: an overview of systematic reviews and meta-analyses.亚甲基四氢叶酸还原酶多态性与复发性妊娠丢失的关系:系统评价和荟萃分析概述。
J Assist Reprod Genet. 2019 Jul;36(7):1315-1328. doi: 10.1007/s10815-019-01473-2. Epub 2019 Jun 28.
7
A pilot study of the implementation of pharmacogenomic pharmacist initiated pre-emptive testing in primary care.一项在初级保健中实施药物基因组学药师主导的预先检测的初步研究。
Eur J Hum Genet. 2019 Oct;27(10):1532-1541. doi: 10.1038/s41431-019-0454-x. Epub 2019 Jun 21.
8
Estimated nationwide impact of implementing a preemptive pharmacogenetic panel approach to guide drug prescribing in primary care in The Netherlands.估算在荷兰的初级保健中实施抢先药物遗传学面板方法来指导药物处方的全国性影响。
BMC Med. 2019 Jun 14;17(1):110. doi: 10.1186/s12916-019-1342-5.
9
Pharmacogenetic testing in primary care practice: opinions of physicians, pharmacists and patients.在初级保健实践中进行药物遗传学检测:医生、药剂师和患者的观点。
Pharmacogenomics. 2019 Jun;20(8):589-598. doi: 10.2217/pgs-2019-0004.
10
Preemptive pharmacogenetic testing: exploring the knowledge and perspectives of US payers.预先药物遗传学检测:探索美国支付方的知识和观点。
Genet Med. 2019 May;21(5):1224-1232. doi: 10.1038/gim.2017.181. Epub 2017 Oct 26.