• 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

相似文献

1
Gene-based drug therapy in children.儿童基于基因的药物治疗。
Paediatr Child Health. 2023 Jun 6;28(4):205-251. doi: 10.1093/pch/pxad002. eCollection 2023 Jul.
2
Urgent call for guidance supporting gene-based drug dosing in children and adolescents.紧急呼吁为儿童和青少年基于基因的药物剂量制定提供指导支持。
Paediatr Child Health. 2023 Jun 6;28(4):205-245. doi: 10.1093/pch/pxad003. eCollection 2023 Jul.
3
Pharmacogenomics and adverse effects of anti-infective drugs in children.儿童抗感染药物的药物基因组学与不良反应
Clin Exp Pharmacol Physiol. 2024 Jan;51(1):3-9. doi: 10.1111/1440-1681.13830. Epub 2023 Oct 15.
4
Pharmacogenomics for Drug Dosing in Children: Current Use, Knowledge, and Gaps.儿童药物剂量的药物基因组学:当前的使用、知识和差距。
J Clin Pharmacol. 2021 Jun;61 Suppl 1(Suppl 1):S188-S192. doi: 10.1002/jcph.1891.
5
[Standard technical specifications for methacholine chloride (Methacholine) bronchial challenge test (2023)].[氯化乙酰甲胆碱支气管激发试验标准技术规范(2023年)]
Zhonghua Jie He He Hu Xi Za Zhi. 2024 Feb 12;47(2):101-119. doi: 10.3760/cma.j.cn112147-20231019-00247.
6
Pharmacogenetic actionability and medication prescribing in people with cystic fibrosis.囊性纤维化患者的药物遗传学可操作性和药物处方。
Clin Transl Sci. 2023 Apr;16(4):662-672. doi: 10.1111/cts.13479. Epub 2023 Feb 9.
7
Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice.心血管药物基因组学:当前知识状况及实际应用
Int J Cardiol. 2015 Apr 1;184:772-795. doi: 10.1016/j.ijcard.2015.02.025. Epub 2015 Feb 25.
8
[How to individualize drug therapy based on pharmacogenetic information? A systematic review of published guidelines].[如何基于药物遗传学信息进行个体化药物治疗?已发表指南的系统评价]
Dtsch Med Wochenschr. 2016 Oct;141(21):e183-e202. doi: 10.1055/s-0042-100973. Epub 2016 Oct 17.
9
The Role of Pharmacogenomics in Opioid Prescribing.药物基因组学在阿片类药物处方中的作用。
Curr Treat Options Oncol. 2022 Oct;23(10):1353-1369. doi: 10.1007/s11864-022-01010-x. Epub 2022 Aug 24.
10
Thoughtful Clinical Use of Pharmacogenetics in Child and Adolescent Psychopharmacology.深思熟虑地将药物遗传学应用于儿童和青少年精神药理学的临床实践。
J Am Acad Child Adolesc Psychiatry. 2021 Jun;60(6):660-664. doi: 10.1016/j.jaac.2020.08.006. Epub 2020 Aug 26.

引用本文的文献

1
Moving Away from One-Size-Fits-All: Assessing the Use of Pharmacogenetic-Guided Medication Therapy in Pediatric Patients with Chronic Pain.告别“一刀切”:评估药物遗传学指导的药物治疗在慢性疼痛儿科患者中的应用
Children (Basel). 2025 May 31;12(6):721. doi: 10.3390/children12060721.
2
Gene-based drug therapy for children and youth treated with psychoactive medications.针对使用精神活性药物治疗的儿童和青少年的基因药物疗法。
Paediatr Child Health. 2024 Sep 13;29(5):311-323. doi: 10.1093/pch/pxae029. eCollection 2024 Aug.

本文引用的文献

1
Pharmacogenetics of inhaled long-acting beta2-agonists in asthma: A systematic review.吸入长效β2-激动剂在哮喘中的药物遗传学:系统评价。
Pediatr Allergy Immunol. 2018 Nov;29(7):705-714. doi: 10.1111/pai.12956. Epub 2018 Aug 12.
2
Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update.临床药物遗传学实施联盟指南:人类白细胞抗原基因型与卡马西平和奥卡西平的应用:2017 更新版。
Clin Pharmacol Ther. 2018 Apr;103(4):574-581. doi: 10.1002/cpt.1004. Epub 2018 Feb 2.
3
Implementation of Standardized Clinical Processes for TPMT Testing in a Diverse Multidisciplinary Population: Challenges and Lessons Learned.在多元化的多学科人群中实施 TPMT 检测的标准化临床流程:挑战和经验教训。
Clin Transl Sci. 2018 Mar;11(2):175-181. doi: 10.1111/cts.12533. Epub 2018 Jan 19.
4
Cost-effectiveness of pharmacogenetic-guided treatment: are we there yet?药物基因组学指导治疗的成本效益:我们做到了吗?
Pharmacogenomics J. 2017 Oct;17(5):395-402. doi: 10.1038/tpj.2017.21. Epub 2017 Jun 13.
5
Recommendations for genetic testing to reduce the incidence of anthracycline-induced cardiotoxicity.关于基因检测以降低蒽环类药物所致心脏毒性发生率的建议。
Br J Clin Pharmacol. 2016 Sep;82(3):683-95. doi: 10.1111/bcp.13008. Epub 2016 Jun 30.
6
Clinical Practice Recommendations for the Management and Prevention of Cisplatin-Induced Hearing Loss Using Pharmacogenetic Markers.使用药物遗传学标志物管理和预防顺铂所致听力损失的临床实践建议
Ther Drug Monit. 2016 Aug;38(4):423-31. doi: 10.1097/FTD.0000000000000298.
7
A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.RARG基因中的一个编码变异赋予儿童癌症患者对蒽环类药物诱导的心脏毒性的易感性。
Nat Genet. 2015 Sep;47(9):1079-84. doi: 10.1038/ng.3374. Epub 2015 Aug 3.
8
Genetic variants in SLC22A17 and SLC22A7 are associated with anthracycline-induced cardiotoxicity in children.溶质载体家族22成员17(SLC22A17)和溶质载体家族22成员7(SLC22A7)中的基因变异与儿童蒽环类药物诱导的心脏毒性相关。
Pharmacogenomics. 2015;16(10):1065-76. doi: 10.2217/pgs.15.61. Epub 2015 Jul 31.
9
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP3A5 Genotype and Tacrolimus Dosing.临床药物基因组学实施联盟(CPIC)关于CYP3A5基因分型与他克莫司给药的指南。
Clin Pharmacol Ther. 2015 Jul;98(1):19-24. doi: 10.1002/cpt.113. Epub 2015 Jun 3.
10
Pharmacogenomics of antimicrobial agents.抗菌药物的药物基因组学
Pharmacogenomics. 2014;15(15):1903-30. doi: 10.2217/pgs.14.147.

儿童基于基因的药物治疗。

Gene-based drug therapy in children.

作者信息

Rassekh S Rod, Rieder Michael, 't Jong Geert

机构信息

Canadian Paediatric Society, Drug Therapy and Hazardous Substances Committee, Ottawa, Ontario, Canada.

出版信息

Paediatr Child Health. 2023 Jun 6;28(4):205-251. doi: 10.1093/pch/pxad002. eCollection 2023 Jul.

DOI:10.1093/pch/pxad002
PMID:37287477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10243977/
Abstract

The past two decades have seen enormous advancements in medical knowledge around the role of genetic factors of variability, both in human disease and drug response. This knowledge is increasingly being translated into guidelines that inform drug dosing, monitoring for efficacy and safety, and determining the suitability of specific agents to treat patients. Health Canada and the U.S. Food and Drug Administration have recommended using genetic information to guide dosing for more than 20 drugs. There are no current, comprehensive paediatric guidelines to assist health care professionals in the use of genetics to inform medication dosing, safety, and efficacy in children, and such guidance is urgently needed. This statement helps to guide clinician understanding of the role of pharmacogenetics and how to use this information when prescribing medications in paediatrics.

摘要

在过去二十年里,围绕人类疾病和药物反应中基因变异因素所起的作用,医学知识取得了巨大进展。这些知识越来越多地被转化为指导原则,用于指导药物剂量、疗效和安全性监测,以及确定特定药物治疗患者的适用性。加拿大卫生部和美国食品药品监督管理局已建议使用基因信息来指导20多种药物的剂量调整。目前尚无全面的儿科指南来帮助医疗保健专业人员利用遗传学知识指导儿童用药的剂量、安全性和疗效,而此类指导意见迫切需要。本声明有助于指导临床医生理解药物遗传学的作用,以及在儿科开处方时如何使用这些信息。