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2
Impact of DNA source on genetic variant detection from human whole-genome sequencing data.DNA 来源对人类全基因组测序数据中遗传变异检测的影响。
J Med Genet. 2019 Dec;56(12):809-817. doi: 10.1136/jmedgenet-2019-106281. Epub 2019 Sep 12.
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Evaluation of buccal swabs for pharmacogenetics.用于药物遗传学的口腔拭子评估
BMC Res Notes. 2018 Jun 14;11(1):382. doi: 10.1186/s13104-018-3476-5.
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Clinical pharmacogenetics implementation consortium guideline (CPIC) for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants: 2016 update.临床药物基因组学实施联盟指南(CPIC):CYP2D6 和 CYP2C19 基因型与三环类抗抑郁药剂量:2016 年更新。
Clin Pharmacol Ther. 2017 Jul;102(1):37-44. doi: 10.1002/cpt.597. Epub 2017 Feb 13.
5
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP2C19 and Voriconazole Therapy.临床药物遗传学实施联盟(CPIC) CYP2C19 和伏立康唑治疗指南。
Clin Pharmacol Ther. 2017 Jul;102(1):45-51. doi: 10.1002/cpt.583. Epub 2017 Apr 18.
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Epidemiology of Polypharmacy and Potential Drug-Drug Interactions Among Pediatric Patients in ICUs of U.S. Children's Hospitals.美国儿童医院重症监护病房儿科患者多重用药及潜在药物相互作用的流行病学
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7
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8
Clinical Characteristics and Immediate-Outcome of Children Mechanically Ventilated in PICU of Pakistan.巴基斯坦儿科重症监护病房机械通气患儿的临床特征和即刻转归。
Pak J Med Sci. 2014 Sep;30(5):927-30. doi: 10.12669/pjms.305.5159.
9
Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450 2D6 genotype and codeine therapy: 2014 update.临床药物遗传学实施联盟 CYP2D6 基因型和可待因治疗指南:2014 年更新。
Clin Pharmacol Ther. 2014 Apr;95(4):376-82. doi: 10.1038/clpt.2013.254. Epub 2014 Jan 23.
10
Genotyping performance between saliva and blood-derived genomic DNAs on the DMET array: a comparison.唾液和血液来源基因组 DNA 在 DMET 阵列上的基因分型性能比较:一项对比研究。
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气管吸出物作为机械通气儿科患者药物基因组学检测的替代生物样本。

Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric Patients.

机构信息

Division of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

Clin Transl Sci. 2021 Mar;14(2):497-501. doi: 10.1111/cts.12847. Epub 2021 Jan 25.

DOI:10.1111/cts.12847
PMID:32702149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7993287/
Abstract

Patients in the pediatric intensive care unit are exposed to multiple medications and are at high risk for adverse drug reactions. Pharmacogenomic (PGx) testing could help decrease their risk of adverse reactions. Although whole blood is preferred for PGx testing, blood volume in this population is often limited. However, for patients on mechanical ventilation, tracheal secretions are abundant, frequently suctioned, and discarded. Thus, the aim of this pilot study was to determine if tracheal aspirates could be used as a source of human genomic DNA for PGx testing. We successfully extracted DNA from tracheal secretions of all 23 patients in the study. The samples were successfully genotyped for 10 clinically actionable single nucleotide variants across 3 cytochrome P450 genes (CYP2D6, CYP2C19, and CYP3A5). Using DNA from whole blood samples in 11 of the patients, we confirmed the accuracy of the genotyping with 100% concordance. Therefore, our results support the use of tracheal aspirates from mechanically ventilated children as an adequate biospecimen for clinical genetic testing.

摘要

儿科重症监护病房的患者会接触多种药物,且发生药物不良反应的风险很高。药物基因组学(PGx)检测有助于降低他们发生不良反应的风险。尽管全血是 PGx 检测的首选,但该人群的血容量往往有限。然而,对于接受机械通气的患者,气管分泌物丰富,经常被抽吸和丢弃。因此,本试点研究旨在确定气管吸出物是否可用作 PGx 检测的人类基因组 DNA 来源。我们成功地从研究中的 23 名患者的气管分泌物中提取了 DNA。对 3 个细胞色素 P450 基因(CYP2D6、CYP2C19 和 CYP3A5)的 10 个具有临床意义的单核苷酸变异进行了基因分型,所有样本均成功分型。使用 11 名患者的全血样本中的 DNA,我们以 100%的一致性证实了基因分型的准确性。因此,我们的研究结果支持使用机械通气儿童的气管吸出物作为临床遗传检测的合适生物样本。