Austin C Adrian, Szeto Andy, Gupta Apoorva, Wiltshire Timothy, Crona Daniel J, Kistler Christine
Division of Pulmonary and Critical Care Medicine, Division of Geriatric Medicine, Department of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Division of Geriatric Medicine, Department of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
J Pharm Technol. 2022 Aug;38(4):195-201. doi: 10.1177/87551225221085116. Epub 2022 Apr 13.
Pharmacogenetics may explain a substantial proportion of the variation seen in the efficacy and risk profile of analgesosedative drugs and the incidence of delirium in critically ill adults. Conduct a feasibility study to demonstrate the reliability of collecting and analyzing pharmacogenetic information from critically ill patients and to assess the impact of pharmacogenetics on intensive care unit (ICU) outcomes. We prospectively enrolled subjects from the Medical ICU at the University of North Carolina (UNC). DNA was obtained via a buccal swab and evaluated using the DNA2Rx assay. We collected data on demographics, daily cumulative psychoactive medication exposure, and severity of illness. We performed daily delirium assessments via the CAM-ICU. We analyzed associations between select single nucleotide polymorphisms (SNPs) and delirium. From June, 2018 through January, 2019, we screened 244 patients and enrolled 50. The median age was 62.0 years old (range: 28-82 years old), and 27 (54%) of the subjects were female. In all, 49 (98%) samples were both high quality and sufficient quantity. In secondary analyses, we found that 80% (12/15) of patients with two 2 copies of a G allele at rs4680 on COMT experienced delirium, whereas 44% (4/9) of patients with 2 copies of an A allele at this location had delirium. In all, 44% (4/9) of patients with 2 T allele copies at rs7439366 on UGT2B7 experienced delirium compared to 73% (11/15) of patients with 2 C allele copies at this location. We can feasibly collect genetic information from critically ill adults. We were able to efficiently collect high quality DNA of sufficient quantity to conduct pharmacogenetic analysis in this critically ill population. Although the sample size of our current study is too small to conduct robust inferential analyses, it suggests potential SNP targets for a future larger study.
药物遗传学可能解释了镇痛镇静药物疗效和风险特征以及危重症成年患者谵妄发生率中很大一部分的差异。开展一项可行性研究,以证明从危重症患者中收集和分析药物遗传学信息的可靠性,并评估药物遗传学对重症监护病房(ICU)结局的影响。我们前瞻性地纳入了北卡罗来纳大学(UNC)医学重症监护病房的受试者。通过口腔拭子获取DNA,并使用DNA2Rx检测法进行评估。我们收集了人口统计学数据、每日累积精神活性药物暴露情况以及疾病严重程度的数据。我们通过CAM-ICU进行每日谵妄评估。我们分析了特定单核苷酸多态性(SNP)与谵妄之间的关联。从2018年6月到2019年1月,我们筛查了244例患者,纳入了50例。中位年龄为62.0岁(范围:28 - 82岁),27例(54%)受试者为女性。总共49份(98%)样本质量高且数量充足。在二次分析中,我们发现儿茶酚-O-甲基转移酶(COMT)基因rs4680位点有两个G等位基因拷贝的患者中,80%(12/15)发生了谵妄,而该位点有两个A等位基因拷贝的患者中,44%(4/9)发生了谵妄。总共,尿苷二磷酸葡萄糖醛酸基转移酶2B7(UGT2B7)基因rs7439366位点有两个T等位基因拷贝的患者中,44%(4/9)发生了谵妄,而该位点有两个C等位基因拷贝的患者中,73%(11/15)发生了谵妄。我们可以切实可行地从危重症成年患者中收集基因信息。我们能够有效地收集到高质量且数量充足的DNA,以便在这个危重症人群中进行药物遗传学分析。尽管我们当前研究的样本量太小,无法进行有力的推断性分析,但它为未来更大规模的研究提示了潜在的SNP靶点。