白藜芦醇治疗阿尔茨海默病的临床疗效及药理机制研究。

Sian Jin, Xuefeng Guan, Dongyu Min
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引用次数: 0

摘要

背景:评价白藜芦醇治疗阿尔茨海默病(AD)的疗效及药理机制。方法:我们利用可访问的开放数据库,对现有的有关白藜芦醇治疗阿尔茨海默病患者的随机对照试验进行了深入的探索。定量变量用标准化平均差(SMD)表示,并伴有95%置信区间(CI)。此外,我们使用网络药理学技术研究了与白藜芦醇对阿尔茨海默病影响相关的潜在靶点和可能的途径。结果:我们的荟萃分析包括5项试验,涉及271例AD患者,其中139例接受白藜芦醇治疗,132例接受安慰剂治疗。与安慰剂治疗相比,白藜芦醇治疗导致阿尔茨海默病合作研究-日常生活活动(ADAS-ADL)评分显著改善(SMD=0.51;95% CI, 0.24 ~ 0.78)和脑脊液(CSF) Aβ40 (SMD=0.84;95% CI, 0.21 ~ 1.47)和血浆Aβ40水平(SMD=0.43;95% CI, 0.07 ~ 0.79)。然而,与安慰剂治疗组相比,白藜芦醇治疗组在迷你精神状态检查(MMSE)评分、脑脊液Aβ42和血浆Aβ42水平以及脑容量方面的改善不显著。两组间不良反应发生率无显著统计学差异。网络药理学结果显示,白藜芦醇与阿尔茨海默病的主要富集相互作用通路主要集中在PI3K信号通路内。白藜芦醇治疗AD的潜在关键靶点包括MAKP1、HRAS、EGFR和MAPK2K1。结论:白藜芦醇在具有较高安全性的同时,对AD患者有一定的疗效,未来还需要更多的数据来验证白藜芦醇治疗AD的疗效。抑制PI3K信号通路在使用白藜芦醇治疗AD患者中可能具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence of Clinical Efficacy and Pharmacological Mechanisms of Resveratrol in the Treatment of Alzheimer's Disease.

Background: To evaluate the efficacy and pharmacological mechanisms of resveratrol in Alzheimer's disease (AD) patients.

Methods: We conducted a thorough exploration of existing randomized controlled trials concerning the treatment of Alzheimer's disease patients using resveratrol, utilizing accessible open databases. Quantitative variables were represented as a standardized mean difference (SMD), accompanied by a 95% confidence interval (CI). Additionally, we examined the potential targets and plausible pathways associated with the impact of resveratrol on Alzheimer's disease using network pharmacology techniques.

Results: Our meta-analysis comprised five trials involving 271 AD patients, of whom 139 received resveratrol treatment and 132 received placebo treatment. Compared with placebo therapy, resveratrol treatment resulted in a significant improvement in Alzheimer's Disease Cooperative Study- Activities of Daily Living (ADAS-ADL) scores (SMD=0.51; 95% CI, 0.24 to 0.78) and cerebrospinal fluid (CSF) Aβ40 (SMD=0.84; 95% CI, 0.21 to 1.47) and plasma Aβ40 levels (SMD=0.43; 95% CI, 0.07 to 0.79). However, the improvement in the resveratrol-treated group compared with the placebo treatment group on the Mini-Mental State Examination (MMSE) score, CSF Aβ42 and plasma Aβ42 levels, and brain volume was not significant. There were no noteworthy statistical variances in the occurrence of adverse effects noted between the two groups. The outcomes of network pharmacology divulged that the principal enriched interaction pathway between resveratrol and Alzheimer's disease is primarily concentrated within the PI3K signaling pathways. Resveratrol's potential key targets for the treatment of AD include MAKP1, HRAS, EGFR, and MAPK2K1.

Conclusion: While having a high safety profile, resveratrol has efficacy in AD patients to a certain extent, and more data are required to validate the efficacy of resveratrol for the treatment of AD in the future. Suppression of the PI3K signaling pathways could hold significant importance in the treatment of AD patients using resveratrol.

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