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Alzheimer disease: CSF biomarkers could be used in Aβ immunotherapy trials for AD

机译:阿尔茨海默氏病:脑脊液生物标记物可用于AD的Aβ免疫疗法试验

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The core cerebrospinal fluid (CSF) biomarkers of Alzheimer disease (AD) -amyloid-beta(Abeta), total tau (t-tau) and phosphorylated tau (p-tau)-have been considered for use as biomarkers in clinical trials to monitor the therapeutic effects of drugs, but clinical data on their suitability for this function has been limited. In a study published in Archives of Neurology, Kaj Blennow and colleagues now show that immunotherapy with the Abeta-specific monoclonal antibody bapineuzumab reduces CSF t-tau and p-tau biomarker levels in patients with mild to moderate AD. "These findings suggest that [bapineuzumab] attenuates the intensity of the neurodegenerative process [in patients with AD]" says Blennow.In two phase II, multicentre, double-blind trials, 46 patients were randomly assigned to receive bapineuzumab (n=27) or placebo (n = 19) for 12 months. CSF samples were collected by lumbar puncture,and the levels of t-tau, p-tau and Abeta were measured with ELISA at baseline and at the end of the study.
机译:阿尔茨海默病(AD)的核心脑脊液(CSF)生物标志物-淀粉样-β(Abeta),总tau(t-tau)和磷酸化tau(p-tau)-在临床试验中已考虑用作生物标志物以监测药物的治疗效果,但有关其对这种功能的适用性的临床数据仍然有限。在《神经病学档案》上发表的一项研究中,Kaj Blennow及其同事现在表明,使用Abeta特异性单克隆抗体bapineuzumab进行免疫治疗可降低轻度至中度AD患者的CSF t-tau和p-tau生物标志物水平。 Blennow表示:“这些发现表明[bapineuzumab]减弱了[AD患者]的神经退行性过程的强度。”在两个II期,多中心,双盲试验中,随机分配了46名患者接受bapineuzumab治疗(n = 27)或安慰剂(n = 19)治疗12个月。通过腰椎穿刺收集脑脊液样品,并在基线和研究结束时通过ELISA测量t-tau,p-tau和Abeta水平。

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