Department of Pharmacology and Toxicology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Internal Medicine, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Eur J Clin Pharmacol. 2023 Oct;79(10):1341-1356. doi: 10.1007/s00228-023-03546-9. Epub 2023 Aug 1.
We assessed the potential effect of CoQ10 administration for the prevention of contrast induced-acute kidney injury (CI-AKI) in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI).
One hundred fifty STEMI patients who were candidates for primary PCI, along with intravenous saline hydration, randomly received a placebo or CoQ10. CoQ10 was administrated orally, 400 mg before the procedure and 200 mg twice daily after the procedure for three consecutive days. Serum creatinine concentration and corresponding creatinine clearance (estimated by the CKD Epidemiology Collaboration (CKD-EPI) creatinine equation) were measured at baseline and 24, 48, and 72 h after primary PCI. Furthermore, the serum level of superoxide dismutase (SOD), total antioxidant capacity (TAC), and malondialdehyde (MDA) was measured before and 72 h after primary PCI.
The mean serum creatinine concentration before contrast administration was similar in the two groups (0.98 ± 0.08 versus 0.99 ± 0.09 mg/dL). While in both study groups, compared to baseline, the mean serum creatinine concentration increased at 48 and 72 h after contrast exposure, the CoQ10 group showed a lower serum creatinine concentration than the placebo group (P-value = 0.017 and 0.004, respectively). However, comparing the mean values of creatinine clearance between the groups at the study time points did not demonstrate a statistically significant difference. CI-AKI, defined as a > 25% or 0.5 mg/dL increase in baseline serum creatinine concentration, occurred in 8.00% of the cases in the CoQ10 group versus 20.00% in the placebo group (P-value = 0.034). Furthermore, at 72 h, the CoQ10-treated group exhibited higher serum levels of SOD and TAC and a lower MDA level than the placebo-treated group.
Our research's findings proposed CoQ10 supplementation as an adjuvant to saline hydration as a preventive approach against CI-AKI.
The trial was registered at Iranian Registry of Clinical Trials ( https://www.irct.ir/trial/60435 , identifier code: IRCT20120215009014N414). Registration date: 2021-12-29.
我们评估了辅酶 Q10 给药预防 ST 段抬高型心肌梗死(STEMI)患者行直接经皮冠状动脉介入治疗(PCI)时对比剂诱导的急性肾损伤(CI-AKI)的潜在效果。
150 名 STEMI 患者为直接 PCI 候选者,在静脉生理盐水水化的同时,随机接受安慰剂或辅酶 Q10 治疗。辅酶 Q10 于术前口服,400mg 一次,术后连续 3 天,每天两次,每次 200mg。在直接 PCI 前、后 24、48 和 72 小时测量血清肌酐浓度和相应的肌酐清除率(通过 CKD 流行病学合作组(CKD-EPI)肌酐方程估算)。此外,在直接 PCI 前和后 72 小时测量血清中超氧化物歧化酶(SOD)、总抗氧化能力(TAC)和丙二醛(MDA)的水平。
两组造影前血清肌酐浓度均值相似(0.98±0.08 与 0.99±0.09mg/dL)。虽然在两组中,与基线相比,造影后 48 和 72 小时时,血清肌酐浓度均值升高,但辅酶 Q10 组的血清肌酐浓度低于安慰剂组(P 值分别为 0.017 和 0.004)。然而,在研究时间点比较两组间肌酐清除率的均值,未发现统计学差异。CI-AKI 定义为基线血清肌酐浓度升高>25%或 0.5mg/dL,辅酶 Q10 组有 8.00%的病例发生,安慰剂组有 20.00%(P 值为 0.034)。此外,在 72 小时时,辅酶 Q10 治疗组的血清 SOD 和 TAC 水平升高,MDA 水平降低,与安慰剂治疗组相比差异有统计学意义。
我们的研究结果提出辅酶 Q10 补充剂联合生理盐水水化作为预防 CI-AKI 的辅助治疗方法。
本试验在伊朗临床试验注册中心(https://www.irct.ir/trial/60435,标识符代码:IRCT20120215009014N414)注册。注册日期:2021-12-29。