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一项评估肼屈嗪在早期阿尔茨海默病中疗效的随机临床试验:EHSAN 研究。

A randomized clinical trial evaluating Hydralazine's efficacy in early-stage Alzheimer's disease: The EHSAN Study.

机构信息

Yazd Cardiovascular Research Centre, Non-Communicable Diseases Research Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Adineh Health Clinic, Yazd, Iran.

出版信息

Sci Rep. 2024 Nov 21;14(1):28837. doi: 10.1038/s41598-024-79616-4.

DOI:10.1038/s41598-024-79616-4
PMID:39572624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11582726/
Abstract

Alzheimer's Disease (AD), a neurodegenerative disorder escalating worldwide, remains incurable with existing interventions merely mitigating symptoms. Hydralazine, an antihypertensive agent, has displayed neuroprotective potential in AD animal models via amplification of mitochondrial functionality and stimulation of stress management and repair pathways. Nevertheless, its effectiveness and tolerability in human AD cohorts are yet to be confirmed. This study protocol describes the design of an ongoing, single-center, randomized, triple-blind, placebo-controlled trial to assess hydralazine's effects on cognitive function in mild to moderate -stage AD patients. We will enroll 424 patients aged 50 and older, meeting NINCDS-ADRDA criteria for probable AD with Mini-Mental State Examination scores from 12-26. They'll be randomly assigned to receive either hydralazine HCL (25 mg, thrice daily) or a placebo for 12 months. The primary outcome is the Alzheimer's Disease Assessment Scale change from baseline to 12 months. Secondary outcomes include various measures using Lawton instrumental activities of daily living scale, neuropsychiatry inventory, and caregiver activity survey. This trial will explore the potential benefits and risks of hydralazine in mild to moderate AD treatment. It's the first trial examining hydralazine's impact on mild to moderate -stage AD in human and is registered at the Iranian Registry of Clinical Trials (IRCT20200711048075N1, registered 29/07/2020) and ClinicalTrials.gov (NCT 04,842,552AQ, registered 13/04/2021). Ethics approval was granted by the Research Ethics Committee of the National Institute for Medical Research Development (IR.NIMAD.REC.1398.424), following the SPIRIT Statement guidelines. Findings will be disseminated via peer-reviewed publications and conferences. This inaugural human clinical trial evaluates hydralazine's impact on patients in the mild to moderate AD. Executed with a randomized, triple-blind, placebo-controlled methodology, this study incorporates a significant sample size and an extended monitoring duration. Multiple parameters, including cognitive capabilities, will be assessed. Potential limitations include the inherent homogeneity of the AD cohort, the lack of biomarker assays, and the unpredictable progression of the disease. Notably, the study might not elucidate the protracted effects of hydralazine beyond a 12-month period. Another limitation of our clinical trial is that patients were diagnosed with Alzheimer's disease based solely on clinical evaluation and MRI findings, without the inclusion of specific biomarkers, which may impact the accuracy and specificity of the diagnosis. Trial registration: Iranian Registry of Clinical Trials (IRCT20200711048075N1, registered 29/07/2020) and ClinicalTrials.gov (NCT 04,842,552, registered 13/04/2021).

摘要

阿尔茨海默病(AD)是一种在全球范围内不断加剧的神经退行性疾病,目前尚无有效的治疗方法,现有的干预措施只能缓解症状。肼屈嗪是一种降压药,在 AD 动物模型中显示出神经保护作用,可增强线粒体功能,刺激应激管理和修复途径。然而,其在人类 AD 患者中的疗效和耐受性仍有待证实。本研究方案描述了一项正在进行的、单中心、随机、三盲、安慰剂对照试验的设计,旨在评估肼屈嗪对轻度至中度 AD 患者认知功能的影响。我们将招募 424 名年龄在 50 岁及以上、符合 NINCDS-ADRDA 可能 AD 标准且简易精神状态检查评分在 12-26 分之间的患者。他们将被随机分配接受肼屈嗪 HCL(25mg,每日三次)或安慰剂治疗 12 个月。主要结局是从基线到 12 个月时阿尔茨海默病评估量表的变化。次要结局包括使用 Lawton 工具性日常生活活动量表、神经精神病学库存和照顾者活动调查的各种测量。该试验将探索肼屈嗪在轻度至中度 AD 治疗中的潜在益处和风险。这是第一项在人类中研究肼屈嗪对轻度至中度 AD 影响的试验,并在伊朗临床试验注册中心(IRCT20200711048075N1,注册于 2020 年 7 月 29 日)和 ClinicalTrials.gov(NCT 04,842,552,注册于 2021 年 4 月 13 日)进行了注册。研究伦理委员会批准了这项研究,研究伦理委员会是国家医学研究发展研究所(IR.NIMAD.REC.1398.424)。研究方案遵循了 SPIRIT 声明指南。研究结果将通过同行评议的出版物和会议进行传播。这项首次人体临床试验评估了肼屈嗪对轻度至中度 AD 患者的影响。该试验采用随机、三盲、安慰剂对照的方法进行,纳入了大量患者,并延长了监测时间。将评估认知能力等多个参数。潜在的局限性包括 AD 队列的固有同质性、缺乏生物标志物检测以及疾病的不可预测进展。值得注意的是,该研究可能无法阐明肼屈嗪在 12 个月后更长时间的效果。我们的临床试验的另一个局限性是,患者仅根据临床评估和 MRI 结果诊断为阿尔茨海默病,没有包括特定的生物标志物,这可能会影响诊断的准确性和特异性。试验注册:伊朗临床试验注册中心(IRCT20200711048075N1,注册于 2020 年 7 月 29 日)和 ClinicalTrials.gov(NCT 04,842,552,注册于 2021 年 4 月 13 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7519/11582726/ba184202b75d/41598_2024_79616_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7519/11582726/f9760810cdb7/41598_2024_79616_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7519/11582726/ba184202b75d/41598_2024_79616_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7519/11582726/f9760810cdb7/41598_2024_79616_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7519/11582726/ba184202b75d/41598_2024_79616_Fig2_HTML.jpg

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肼屈嗪通过改善Nrf2激活的细胞应激反应中与衰老和氧化相关的丧失来恢复细胞和晶状体的健康寿命。
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