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大脑中的CYP2D6:对中枢神经系统药物不良反应的潜在影响——ADRED研究结果

CYP2D6 in the Brain: Potential Impact on Adverse Drug Reactions in the Central Nervous System-Results From the ADRED Study.

作者信息

Just Katja S, Dormann Harald, Freitag Mathias, Schurig Marlen, Böhme Miriam, Steffens Michael, Scholl Catharina, Seufferlein Thomas, Graeff Ingo, Schwab Matthias, Stingl Julia C

机构信息

Institute of Clinical Pharmacology, University Hospital of RWTH Aachen, Aachen, Germany.

Central Emergency Department, Hospital Fürth, Fürth, Germany.

出版信息

Front Pharmacol. 2021 May 7;12:624104. doi: 10.3389/fphar.2021.624104. eCollection 2021.

Abstract

Cytochrome P450 (CYP) 2D6 is a polymorphic enzyme expressed in the central nervous system (CNS), important in drug metabolism and with a potentially constitutive role in CNS function such as vigilance. This study aimed to analyze variability in CYP2D6 activity linked to vigilance-related adverse drug reactions (ADRs) in the CNS. A dataset of N = 2939 ADR cases of the prospective multicenter observational trial in emergency departments (EDs) (ADRED; trial registration: DRKS-ID: DRKS00008979) was analyzed. Dizziness as the most frequent reported CNS ADR symptom (12.7% of patients, = 372) related to vigilance was chosen as the outcome. The association of dizziness with CYP2D6 activity markers was analyzed. The number of CYP2D6 substrates taken, a CYP2D6 saturation score (no, moderate, and strong saturation), a CYP2D6 saturation/inhibition score (no, weak, moderate, and strong), and composed CYP2D6 activity using a genotyped subsample ( = 740) calculating additive effects of genotype and CYP2D6 saturation by drug exposure were used as CYP2D6 activity markers. Effects were compared to other frequent nonvigilance-related CNS ADR symptoms (syncope and headache). Secondary analyses were conducted to control for other ADR symptoms frequently associated with dizziness (syncope, nausea, and falls). The majority of all patients (64.5%, = 1895) took at least one drug metabolized by CYP2D6. Around a third took a CNS drug (32.5%, = 955). The chance to present with drug-related dizziness to the ED increased with each CYP2D6 substrate taken by OR 1.11 [1.01-1.23]. Presenting with drug-related dizziness was more likely with CYP2D6 saturation and saturation/inhibition (both OR 1.27 [1.00-1.60]). The composed CYP2D6 activity was positively associated with dizziness ( = 0.028), while poorer activity affected patients more often with dizziness as an ADR. In contrast, nonvigilance-related ADR symptoms such as syncope and nausea were not consistently significantly associated with CYP2D6 activity markers. This study shows an association between the number of CYP2D6 substrates, the predicted CYP2D6 activity, and the occurrence of dizziness as a CNS ADR symptom. As dizziness is a vigilance-related CNS symptom, patients with low CYP2D6 activity might be more vulnerable to drug-related dizziness. This study underlines the need for understanding individual drug metabolism activity and individual risks for ADRs.

摘要

细胞色素P450(CYP)2D6是一种在中枢神经系统(CNS)中表达的多态性酶,在药物代谢中起重要作用,并且在诸如警觉等中枢神经系统功能中可能具有组成性作用。本研究旨在分析与中枢神经系统中与警觉相关的药物不良反应(ADR)相关的CYP2D6活性变异性。分析了急诊科(ED)前瞻性多中心观察性试验(ADRED;试验注册号:DRKS-ID:DRKS00008979)的N = 2939例ADR病例数据集。选择头晕作为最常报告的与警觉相关的中枢神经系统ADR症状(12.7%的患者,n = 372)作为结果。分析了头晕与CYP2D6活性标志物的关联。使用的CYP2D6活性标志物包括服用的CYP2D6底物数量、CYP2D6饱和评分(无、中度和强饱和)、CYP2D6饱和/抑制评分(无、弱、中度和强),以及使用基因分型子样本(n = 740)计算基因型和药物暴露引起的CYP2D6饱和的加性效应来组成CYP2D6活性。将这些效应与其他常见的与警觉无关的中枢神经系统ADR症状(晕厥和头痛)进行比较。进行了二次分析以控制其他经常与头晕相关的ADR症状(晕厥、恶心和跌倒)。所有患者中的大多数(64.5%,n = 1895)服用了至少一种由CYP2D6代谢的药物。大约三分之一的患者服用了中枢神经系统药物(32.5%,n = 955)。因药物相关头晕到急诊科就诊的几率随着服用的每种CYP2D6底物增加而增加,比值比为1.11 [1.01 - 1.23]。出现药物相关头晕在CYP2D6饱和以及饱和/抑制时更有可能(两者比值比均为1.27 [1.00 - 1.60])。组成的CYP2D6活性与头晕呈正相关(P = 0.028),而活性较差的患者更常出现头晕作为ADR。相比之下,与警觉无关的ADR症状如晕厥和恶心与CYP2D6活性标志物没有始终显著关联。本研究表明CYP2D6底物数量、预测的CYP2D6活性与作为中枢神经系统ADR症状的头晕发生之间存在关联。由于头晕是与警觉相关的中枢神经系统症状,CYP2D6活性低的患者可能更容易出现药物相关头晕。本研究强调了了解个体药物代谢活性和个体ADR风险的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7f2/8138470/1982e5d20fc9/fphar-12-624104-g001.jpg

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