Department of Neurology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Clinical Pharmacy, School of Pharmacy, Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Oxid Med Cell Longev. 2022 Jul 29;2022:2493053. doi: 10.1155/2022/2493053. eCollection 2022.
This study was undertaken to evaluate the influence of oral Acetyl-L-carnitine (ALC) in patients with acute ischemic stroke.
Sixty-nine cases with acute ischemic stroke with the onset of symptoms less than 24 hours not candidates for reperfusion therapy were randomly assigned to either the ALC group (1000 mg three times per day for three consecutive days) or the matching placebo group. The study outcomes based on intention-to-treat criteria included the change in the modified Rankin Scale (mRS) and National Institutes of Health Stroke Scale (NIHSS) score from baseline to day 90, as well as the change in serum levels of the inflammatory and oxidative stress biomarkers over the 3-day treatment protocol.
The NIHSS score and mRS score on day 90 were improved by 5.82 and 0.94 scores, respectively, in the ALC-treated group compared to 2.83 and 0.11 scores, respectively, in the placebo-treated group, which demonstrated the superiority of ALC relative to placebo. By using the multivariable analysis after adjusting for other variables in the model, compared to the group treated with placebo, patients in the ALC group had lower NIHSS score (: -2.40, 95% CI: -0.69, -4.10 ( = 0.007)) and mRS score (: -1.18, 95% CI: -0.52, -1.84 ( = 0.001)) 90 days after the intervention. The percentage of patients with a favourable functional outcome at day 90, defined as mRS scores of 0 or 1, was significantly higher in the ALC group in comparison to the placebo group (52.9% versus 28.6%). Further, over the 3-day treatment protocol, in the patients receiving ALC, the serum levels of proinflammatory biomarkers, including soluble intercellular adhesion molecule-1 (sICAM-1), interleukin 6 (IL-6), tumor necrosis factor-alpha (TNF-), and neuron-specific enolase (NSE), showed a significant decrease, while the serum levels of antioxidant biomarkers, including glutathione peroxidase (GPx), superoxide dismutase (SOD), and total antioxidant capacity (TAC), as well as the total L-carnitine's level showed a significant increase compared to those in patients receiving placebo indicating significant alteration.
Although preliminary, these results suggested that ALC administration during the acute phase of ischemic stroke might be helpful in improving functional and neurological outcomes that are probably linked to its anti-inflammatory and antioxidant properties. . This trial is registered with IRCT20150629022965N17 at Iranian Registry of Clinical Trials (registration date: 25/07/2018).
本研究旨在评估口服乙酰左旋肉碱(ALC)对急性缺血性脑卒中患者的影响。
69 例发病 24 小时内且不符合再灌注治疗条件的急性缺血性脑卒中患者,随机分为 ALC 组(1000mg,每日 3 次,连续 3 天)或匹配安慰剂组。基于意向治疗原则的研究结局包括:从基线到 90 天改良 Rankin 量表(mRS)和美国国立卫生研究院卒中量表(NIHSS)评分的变化,以及治疗 3 天期间血清炎症和氧化应激生物标志物水平的变化。
与安慰剂组相比,ALC 治疗组 90 天时 NIHSS 评分和 mRS 评分分别改善了 5.82 分和 0.94 分,这表明 ALC 优于安慰剂。通过调整模型中其他变量的多变量分析,与安慰剂组相比,ALC 组的 NIHSS 评分(:-2.40,95%CI:-0.69,-4.10(=0.007))和 mRS 评分(:-1.18,95%CI:-0.52,-1.84(=0.001))在干预后 90 天均较低。与安慰剂组相比,90 天时 ALC 组有更多的患者获得良好的功能结局(定义为 mRS 评分为 0 或 1),比例明显更高(52.9%比 28.6%)。此外,在接受 ALC 治疗的患者中,在治疗 3 天期间,促炎生物标志物,包括可溶性细胞间黏附分子-1(sICAM-1)、白细胞介素 6(IL-6)、肿瘤坏死因子-α(TNF-α)和神经元特异性烯醇化酶(NSE)的血清水平显著下降,而抗氧化生物标志物,包括谷胱甘肽过氧化物酶(GPx)、超氧化物歧化酶(SOD)和总抗氧化能力(TAC)以及总左旋肉碱水平显著升高,这表明发生了显著变化。
尽管初步结果,但这些结果表明,在缺血性脑卒中急性期给予 ALC 可能有助于改善功能和神经结局,这可能与其抗炎和抗氧化特性有关。这项试验在伊朗临床试验注册中心(IRCT)注册,注册号为 IRCT20150629022965N17(注册日期:2018 年 7 月 25 日)。