Efficacy of High-Dose and Low-Dose Simvastatin on Vascular Oxidative Stress and Neurological Outcomes in Patient with Acute Ischemic Stroke: A Randomized, Double-Blind, Parallel, Controlled Trial.

IF 1.7 Q4 NEUROSCIENCES Neurology Research International Pub Date : 2018-04-18 eCollection Date: 2018-01-01 DOI:10.1155/2018/7268924
Nattaphol Uransilp, Pannawat Chaiyawatthanananthn, Sombat Muengtaweepongsa
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Abstract

Backgrounds: Stroke is the leading cause of death and long-term disability. Oxidative stress is elevated during occurrence of acute ischemic stroke (AIS). Soluble LOX-1 (sLOX-1) and NO are used as biomarkers for vascular oxidative stress that can reflect stabilization of atherosclerotic plaque. Previous study showed that simvastatin can reduce oxidative stress and LOX-1 expression.

Objectives: To evaluate neurological outcomes and serum sLOX-1 and NO levels in patients with AIS treatment with low dose 10 mg/day and high dose 40 mg/day of simvastatin.

Methods: 65 patients with AIS within 24 hours after onset were randomized to treatment with simvastatin 10 mg/day or 40 mg/day for 90 days. Personal data and past history of all patients were recorded at baseline. The blood chemistries were measured by standard laboratory techniques. Serum sLOX-1 and NO levels and neurological outcomes including NIHSS, mRS, and Barthel index were tested at baseline and Day 90 after simvastatin therapy.

Results: Baseline characteristics were not significantly different in both groups except history of hypertension. Serum sLOX-1 and NO levels significantly reduce in both groups (sLOX-1 = 1.19 ± 0.47 and 0.98 ± 0.37 ng/ml; NO = 49.28 ± 7.21 and 46.59 ± 9.36 μmol/l) in 10 mg/day and 40 mg/day simvastatin groups, respectively. Neurological outcomes including NIHSS, mRS, and Barthel index significantly improve in both groups. However, no difference in NO level and neurological outcomes was found at 90 days after treatment as compared between low dose 10 mg/day and high dose 40 mg/day of simvastatin.

Conclusion: High-dose simvastatin might be helpful to reduce serum sLOX-1. But no difference in clinical outcomes was found between high- and low-dose simvastatin. Further more intensive clinical trial is needed to confirm the appropriate dosage of simvastatin in patients with acute ischemic stroke. This trial is registered with ClinicalTrials.gov ID: NCT03402204.

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大剂量和小剂量辛伐他汀对急性缺血性脑卒中患者血管氧化应激和神经功能预后的疗效:一项随机、双盲、平行对照试验。
背景:中风是导致死亡和长期残疾的主要原因。急性缺血性中风(AIS)发生时氧化应激升高。可溶性 LOX-1(sLOX-1)和 NO 是血管氧化应激的生物标志物,可反映动脉粥样硬化斑块的稳定性。先前的研究表明,辛伐他汀可降低氧化应激和 LOX-1 的表达:方法:65例发病24小时内的AIS患者随机接受辛伐他汀10毫克/天或40毫克/天的治疗,为期90天。所有患者的个人资料和既往病史均在基线时记录。采用标准实验室技术测量血液化学成分。在辛伐他汀治疗后的基线和第90天检测血清sLOX-1和NO水平以及神经系统结果,包括NIHSS、mRS和Barthel指数:结果:除高血压病史外,两组患者的基线特征无明显差异。辛伐他汀10毫克/天组和40毫克/天组的血清sLOX-1和NO水平分别明显降低(sLOX-1=1.19±0.47和0.98±0.37纳克/毫升;NO=49.28±7.21和46.59±9.36微摩尔/升)。两组患者的神经功能结果(包括 NIHSS、mRS 和 Barthel 指数)均明显改善。然而,与低剂量辛伐他汀(10 毫克/天)和高剂量辛伐他汀(40 毫克/天)相比,在治疗 90 天后,NO 水平和神经功能结果均无差异:结论:大剂量辛伐他汀可能有助于降低血清sLOX-1。结论:高剂量辛伐他汀可能有助于降低血清 sLOX-1,但高剂量和低剂量辛伐他汀的临床结果没有差异。需要进一步开展更深入的临床试验,以确定辛伐他汀在急性缺血性脑卒中患者中的合适剂量。该试验已在 ClinicalTrials.gov ID:NCT03402204。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
10
审稿时长
17 weeks
期刊介绍: Neurology Research International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on diseases of the nervous system, as well as normal neurological functioning. The journal will consider basic, translational, and clinical research, including animal models and clinical trials.
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