CAPES Foundation, Ministry of Education of Brazil, Brasília DF 70040-020, Brazil.
Aix Marseille Université, INSERM, C2VN, 13005 Marseille, France.
Toxins (Basel). 2019 Apr 7;11(4):209. doi: 10.3390/toxins11040209.
Chronic kidney disease (CKD) is a major public health problem, since 300,000,000 people in the world display a glomerular filtration rate (GFR) below 60 mL/min/1.73m². Patients with CKD have high rates of complications and comorbidities. Thus, they require the prescription of numerous medications, making the management of patients very complex. The prescription of numerous drugs associated with an altered renal- and non-renal clearance makes dose adjustment challenging in these patients, with frequent drug-related adverse events. However, the mechanisms involved in this abnormal drug clearance during CKD are not still well identified. We propose here that the transcription factor, aryl hydrocarbon receptor, which is the cellular receptor for indolic uremic toxins, could worsen the metabolism and the excretion of drugs in CKD patients.
慢性肾脏病(CKD)是一个主要的公共卫生问题,因为全球有 3 亿人肾小球滤过率(GFR)低于 60mL/min/1.73m²。CKD 患者有很高的并发症和合并症发生率。因此,他们需要开很多药,这使得患者的管理非常复杂。这些患者的许多药物与改变的肾和非肾清除相关联,这使得剂量调整具有挑战性,并且经常发生药物相关的不良反应。然而,在 CKD 期间涉及这种异常药物清除的机制尚未完全确定。我们在这里提出,转录因子芳香烃受体,它是吲哚尿毒素的细胞受体,可能会使 CKD 患者的药物代谢和排泄恶化。