Kerskes Catharina H M, van den Eijnde Carien J M E, Aarnoudse Albert-Jan L H J, Grouls René J E, Deiman Birgit A L M, Deenen Maarten J
Department of Clinical Pharmacy, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands.
Faculty of Pharmacy, University Utrecht, 3508 TB Utrecht, The Netherlands.
Pharmacy (Basel). 2023 Apr 4;11(2):69. doi: 10.3390/pharmacy11020069.
Patients with chronic kidney disease (CKD) stage 3-5 are polypharmacy patients. Many of these drugs are metabolized by cytochrome P450 () and Genetic polymorphism is well known to result in altered drug metabolism capacity. This study determined the added value of pharmacogenetic testing to the routine medication evaluation in polypharmacy patients with CKD. In adult outpatient polypharmacy patients with CKD3-5 disease, a pharmacogenetic profile was determined. Then, automated medication surveillance for gene-drug interactions was performed based on the pharmacogenetic profile and the patients' current prescriptions. Of all identified gene-drug interactions, the hospital pharmacist and the treating nephrologist together assessed clinical relevance and necessity of a pharmacotherapeutic intervention. The primary endpoint of the study was the total number of applied pharmacotherapeutic interventions based on a relevant gene-drug interaction. A total of 61 patients were enrolled in the study. Medication surveillance resulted in a total of 66 gene-drug interactions, of which 26 (39%) were considered clinically relevant. This resulted in 26 applied pharmacotherapeutic interventions in 20 patients. Systematic pharmacogenetic testing enables pharmacotherapeutic interventions based on relevant gene-drug interactions. This study showed that pharmacogenetic testing adds to routine medication evaluation and could lead to optimized pharmacotherapy in CKD patients.
慢性肾脏病(CKD)3 - 5期患者属于多重用药患者。这些药物中的许多是通过细胞色素P450()代谢的,并且已知基因多态性会导致药物代谢能力改变。本研究确定了药物遗传学检测在CKD多重用药患者常规药物评估中的附加价值。在成年门诊CKD3 - 5期多重用药患者中,确定了药物遗传学特征。然后,根据药物遗传学特征和患者当前的处方进行基因 - 药物相互作用的自动药物监测。对于所有识别出的基因 - 药物相互作用,医院药剂师和主治肾病专家共同评估药物治疗干预的临床相关性和必要性。该研究的主要终点是基于相关基因 - 药物相互作用应用的药物治疗干预总数。共有61名患者纳入该研究。药物监测共发现66种基因 - 药物相互作用,其中26种(39%)被认为具有临床相关性。这导致20名患者应用了26次药物治疗干预。系统的药物遗传学检测能够基于相关基因 - 药物相互作用进行药物治疗干预。本研究表明,药物遗传学检测可补充常规药物评估,并可能使CKD患者的药物治疗得到优化。