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Neuroimaging basis in the conversion of aMCI patients with APOE-ε4 to AD: study protocol of a prospective diagnostic trial

机译:aMCI患有APOE-ε4的aMCI患者向AD转化的神经影像基础:一项前瞻性诊断试验的研究方案

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Background The ε4 allele of the Apolipoprotein E gene (APOE-ε4) is a potent genetic risk factor for sporadic Alzheimer’s disease (AD). Amnestic mild cognitive impairment (aMCI) is an intermediate state between normal cognitive aging and dementia, which is easy to convert to AD dementia. It is an urgent problem in the field of cognitive neuroscience to reveal the conversion of aMCI-ε4 to AD. Based on our preliminary work, we will study the neuroimaging features in the special group of aMCI-ε4 with multi-modality magnetic resonance imaging (structural MRI, resting state-fMRI and diffusion tensor imaging) longitudinally. Methods/Design In this study, 200 right-handed subjects who are diagnosed as aMCI with APOE-ε4 will be recruited at the memory clinic of the Neurology Department, XuanWu Hospital, Capital Medical University, Beijing, China. All subjects will undergo the neuroimaging and neuropsychological evaluation at a 1?year-interval for 3?years. The primary outcome measures are 1) Microstructural alterations revealed with multimodal MRI scans including structure MRI (sMRI), resting state functional MRI (rs-fMRI), diffusion tensor imaging (DTI); 2) neuropsychological evaluation, including the World Health Organization-University of California-LosAngeles Auditory Verbal Learning Test (WHO-UCLA AVLT), Addenbrook’s cognitive examination-revised (ACE-R), mini-mental state examination (MMSE), Montreal Cognitive Assessment (MoCA), Clinical Dementia Rating scale (CDR). Discussion This study is to find out the neuroimaging biomarker and the changing laws of the marker during the progress of aMCI-ε4 to AD, and the final purpose is to provide scientific evidence for new prevention, diagnosis and treatment of AD. Trial Registration This study has been registered to ClinicalTrials.gov (NCT02225964, https://www.clinicaltrials.gov/ ) in August 24, 2014.
机译:背景载脂蛋白E基因的ε4等位基因(APOE-ε4)是散发性阿尔茨海默氏病(AD)的潜在遗传危险因素。轻度轻度认知障碍(aMCI)是正常认知老化和痴呆之间的一种中间状态,很容易转变为AD痴呆。揭示aMCI-ε4向AD的转化是认知神经科学领域的迫切问题。在我们的初步工作的基础上,我们将纵向研究aMCI-ε4特殊组的神经影像学特征,包括多模态磁共振成像(结构MRI,静止状态fMRI和扩散张量成像)。方法/设计在这项研究中,将在北京首都医科​​大学宣武医院神经内科的记忆科招募200名被诊断为aMCI患有APOE-ε4的右撇子受试者。所有受试者将以1年间隔3年进行神经成像和神经心理学评估。主要结果指标是:1)通过多模式MRI扫描发现的微结构改变,包括结构MRI(sMRI),静止状态功能性MRI(rs-fMRI),扩散张量成像(DTI); 2)神经心理学评估,包括世界卫生组织-加利福尼亚大学-洛杉矶听觉语言学习测验(WHO-UCLA AVLT),Addenbrook的认知检查修订(ACE-R),小精神状态检查(MMSE),蒙特利尔认知评估(MoCA),临床痴呆评定量表(CDR)。讨论本研究旨在了解aMCI-ε4向AD进展过程中的神经影像生物标志物和标志物的变化规律,最终目的是为AD的新的预防,诊断和治疗提供科学依据。试验注册该研究已于2014年8月24日注册到ClinicalTrials.gov(NCT02225964,https://www.clinicaltrials.gov/)。

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