• 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

精准医学融入临床实践:一种基于网络的工具可实现对精神疾病个性化治疗的实时药物遗传学评估。

Precision Medicine into Clinical Practice: A Web-Based Tool Enables Real-Time Pharmacogenetic Assessment of Tailored Treatments in Psychiatric Disorders.

作者信息

Zampatti Stefania, Fabrizio Carlo, Ragazzo Michele, Campoli Giulia, Caputo Valerio, Strafella Claudia, Pellicano Clelia, Cascella Raffaella, Spalletta Gianfranco, Petrosini Laura, Caltagirone Carlo, Termine Andrea, Giardina Emiliano

机构信息

Genomic Medicine Laboratory UILDM, IRCCS Fondazione Santa Lucia, 00179 Rome, Italy.

Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.

出版信息

J Pers Med. 2021 Aug 27;11(9):851. doi: 10.3390/jpm11090851.

DOI:10.3390/jpm11090851
PMID:34575628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8471120/
Abstract

The management of neuropsychiatric disorders involves different pharmacological treatments. In order to perform efficacious drug treatments, the metabolism of CYP genes can help to foresee potential drug-drug interactions. The NeuroPGx software is an open-source web-based tool for genotype/diplotype/phenotype interpretation for neuropharmacogenomic purposes. The software provides information about: (i) the genotypes of evaluated SNPs (single nucleotide polymorphisms); (ii) the main diplotypes in CYP genes and corresponding metabolization phenotypes; (iii) the list of neuropsychiatric drugs with recommended dosage adjustment (according to CPIC and DPWG guidelines); (iv) the list of possible (rare) diplotypes and corresponding metabolization phenotypes. The combined application of NeuroPGx software to the OpenArray technology results in an easy, quick, and highly automated device ready to be used in routine clinical practice.

摘要

神经精神疾病的管理涉及不同的药物治疗方法。为了进行有效的药物治疗,CYP基因的代谢情况有助于预测潜在的药物相互作用。NeuroPGx软件是一个基于网络的开源工具,用于神经药物基因组学目的的基因型/双倍型/表型解读。该软件提供以下信息:(i) 评估的单核苷酸多态性(SNP)的基因型;(ii) CYP基因中的主要双倍型及相应的代谢表型;(iii) 建议进行剂量调整的神经精神药物清单(根据CPIC和DPWG指南);(iv) 可能的(罕见的)双倍型清单及相应的代谢表型。将NeuroPGx软件与OpenArray技术联合应用,可形成一种便于使用、快速且高度自动化的设备,随时可用于常规临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/8471120/301d5a487fda/jpm-11-00851-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/8471120/40ac45c3fe3c/jpm-11-00851-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/8471120/301d5a487fda/jpm-11-00851-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/8471120/40ac45c3fe3c/jpm-11-00851-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/8471120/301d5a487fda/jpm-11-00851-g002.jpg

相似文献

1
Precision Medicine into Clinical Practice: A Web-Based Tool Enables Real-Time Pharmacogenetic Assessment of Tailored Treatments in Psychiatric Disorders.精准医学融入临床实践:一种基于网络的工具可实现对精神疾病个性化治疗的实时药物遗传学评估。
J Pers Med. 2021 Aug 27;11(9):851. doi: 10.3390/jpm11090851.
2
Pharmacogenetics Guidelines: Overview and Comparison of the DPWG, CPIC, CPNDS, and RNPGx Guidelines.药物遗传学指南:DPWG、CPIC、CPNDS和RNPGx指南概述与比较
Front Pharmacol. 2021 Jan 25;11:595219. doi: 10.3389/fphar.2020.595219. eCollection 2020.
3
PharmaKU: A Web-Based Tool Aimed at Improving Outreach and Clinical Utility of Pharmacogenomics.药物基因组学知识单元(PharmaKU):一种旨在提高药物基因组学的推广和临床应用的基于网络的工具。
J Pers Med. 2021 Mar 16;11(3):210. doi: 10.3390/jpm11030210.
4
A Web-Based Pharmacogenomics Search Tool for Precision Medicine in Perioperative Care.一种用于围手术期精准医疗的基于网络的药物基因组学搜索工具。
J Pers Med. 2020 Jul 21;10(3):65. doi: 10.3390/jpm10030065.
5
Pharmacogenomic information from CPIC and DPWG guidelines and its application on drug labels.来自CPIC和DPWG指南的药物基因组学信息及其在药品标签上的应用。
Transl Clin Pharmacol. 2020 Dec;28(4):189-198. doi: 10.12793/tcp.2020.28.e18. Epub 2020 Dec 11.
6
Clinical pharmacogenomics in action: design, assessment and implementation of a novel pharmacogenetic panel supporting drug selection for diseases of the central nervous system (CNS).临床药物基因组学的实际应用:一种支持中枢神经系统(CNS)疾病药物选择的新型药物遗传学检测板的设计、评估与实施
J Transl Med. 2021 Apr 15;19(1):151. doi: 10.1186/s12967-021-02816-3.
7
[Personalised pharmacogenetics. Evidence-based guidelines and clinical application of pharmacogenetic diagnostics].[个性化药物遗传学。药物遗传学诊断的循证指南及临床应用]
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013 Nov;56(11):1509-21. doi: 10.1007/s00103-013-1822-2.
8
Reduced Function Variants and Genotype/Phenotype Translations of CYP2D6 Intermediate Metabolizers: Implications for Personalized Drug Dosing in Psychiatry.CYP2D6中间代谢者的功能降低变体及基因型/表型转化:对精神病学个性化药物剂量的影响
Front Pharmacol. 2021 Apr 22;12:650750. doi: 10.3389/fphar.2021.650750. eCollection 2021.
9
Epistasis between IGF2R and ADAMTS19 polymorphisms associates with premature ovarian failure.IGF2R 和 ADAMTS19 多态性之间的上位性与卵巢早衰有关。
Hum Reprod. 2013 Nov;28(11):3146-54. doi: 10.1093/humrep/det365. Epub 2013 Sep 7.
10
Evaluation of Current Regulation and Guidelines of Pharmacogenomic Drug Labels: Opportunities for Improvements.评价当前药物基因组学标签的法规和指南:改进的机会。
Clin Pharmacol Ther. 2020 May;107(5):1240-1255. doi: 10.1002/cpt.1720. Epub 2019 Dec 17.

引用本文的文献

1
Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample Monitoring.样本追踪工具:一种基于OpenArray技术和R脚本的基因组样本监测综合方法。
Diagnostics (Basel). 2025 Jan 10;15(2):149. doi: 10.3390/diagnostics15020149.
2
Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients.甲基化水平结合机器学习管道突出单个 CpG 位点作为 FSHD 患者的鉴别生物标志物。
Cells. 2022 Dec 18;11(24):4114. doi: 10.3390/cells11244114.
3
WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic Factors.

本文引用的文献

1
Tools for optimising pharmacotherapy in psychiatry (therapeutic drug monitoring, molecular brain imaging and pharmacogenetic tests): focus on antidepressants.精神医学中优化药物治疗的工具(治疗药物监测、分子脑成像和药物遗传学检测):关注抗抑郁药。
World J Biol Psychiatry. 2021 Oct;22(8):561-628. doi: 10.1080/15622975.2021.1878427. Epub 2021 May 12.
2
Pharmacogenetics of Carbamazepine and Valproate: Focus on Polymorphisms of Drug Metabolizing Enzymes and Transporters.卡马西平和丙戊酸盐的药物遗传学:聚焦于药物代谢酶和转运体的多态性
Pharmaceuticals (Basel). 2021 Mar 1;14(3):204. doi: 10.3390/ph14030204.
3
Pharmacogenomic information from CPIC and DPWG guidelines and its application on drug labels.
WARE:湿性年龄相关性黄斑变性风险评估工具作为整合遗传和非遗传因素的临床决策支持系统
J Pers Med. 2022 Jun 24;12(7):1034. doi: 10.3390/jpm12071034.
来自CPIC和DPWG指南的药物基因组学信息及其在药品标签上的应用。
Transl Clin Pharmacol. 2020 Dec;28(4):189-198. doi: 10.12793/tcp.2020.28.e18. Epub 2020 Dec 11.
4
Impact of CYP2D6 on serum concentrations of flupentixol, haloperidol, perphenazine and zuclopenthixol.CYP2D6 对氟哌啶醇、氟奋乃静、奋乃静和氯氮平血清浓度的影响。
Br J Clin Pharmacol. 2021 May;87(5):2228-2235. doi: 10.1111/bcp.14626. Epub 2020 Nov 23.
5
Genotype-Based Dose Recommendations for Risperidone in Asian People.亚洲人群中基于基因型的利培酮剂量推荐
Front Pharmacol. 2020 Aug 4;11:936. doi: 10.3389/fphar.2020.00936. eCollection 2020.
6
The Respective Roles of CYP3A4 and CYP2D6 in the Metabolism of Pimozide to Established and Novel Metabolites.CYP3A4 和 CYP2D6 在匹莫齐特代谢为现有和新代谢物中的各自作用。
Drug Metab Dispos. 2020 Nov;48(11):1113-1120. doi: 10.1124/dmd.120.000188. Epub 2020 Aug 26.
7
CYP2D6 Genetic Polymorphisms and Risperidone Pharmacokinetics: A Systematic Review and Meta-analysis.CYP2D6 基因多态性与利培酮药代动力学:系统评价和荟萃分析。
Pharmacotherapy. 2020 Jul;40(7):632-647. doi: 10.1002/phar.2434. Epub 2020 Jul 12.
8
Associations of CYP2C9 and CYP2C19 Pharmacogenetic Variation with Phenytoin-Induced Cutaneous Adverse Drug Reactions.CYP2C9 和 CYP2C19 药物遗传学变异与苯妥英钠诱导的皮肤不良反应的关联。
Clin Transl Sci. 2020 Sep;13(5):1004-1009. doi: 10.1111/cts.12787. Epub 2020 Apr 18.
9
QuantStudio 12K Flex OpenArray System as a Tool for High-Throughput Genotyping and Gene Expression Analysis.QuantStudio 12K Flex开放式阵列系统作为高通量基因分型和基因表达分析的工具
Methods Mol Biol. 2020;2065:199-208. doi: 10.1007/978-1-4939-9833-3_15.
10
Clopidogrel Pharmacogenetics.氯吡格雷药物遗传学。
Circ Cardiovasc Interv. 2019 Apr;12(4):e007811. doi: 10.1161/CIRCINTERVENTIONS.119.007811.