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一项关于非痴呆性短暂性脑缺血发作患者的神经退行性和小血管疾病以及临床认知轨迹的纵向磁共振成像研究:PREVENT 研究。

A longitudinal magnetic resonance imaging study of neurodegenerative and small vessel disease, and clinical cognitive trajectories in non demented patients with transient ischemic attack: the PREVENT study.

机构信息

Calgary Stroke Program, Department of Clinical Neurosciences, Foothills Medical Centre, 1403 - 29 Street NW, Calgary, AB, Canada.

Seaman Family MR Center, Foothills Medical Centre, 1403 29th Street NW, Calgary, AB, Canada.

出版信息

BMC Geriatr. 2018 Jul 16;18(1):163. doi: 10.1186/s12877-018-0858-4.

Abstract

BACKGROUND

Late-life cognitive decline, caused by progressive neuronal loss leading to brain atrophy years before symptoms are detected, is expected to double in Canada over the next two decades. Cognitive impairment in late life is attributed to vascular and lifestyle related risk factors in mid-life in a substantial proportion of cases (50%), thereby providing an opportunity for effective prevention of cognitive decline if incipient disease is detected earlier. Patients presenting with transient ischemic attack (TIA) commonly display some degree of cognitive impairment and are at a 4-fold increased risk of dementia. In the Predementia Neuroimaging of Transient Ischemic Attack (PREVENT) study, we will address what disease processes (i.e., Alzheimer's vs. vascular disease) lead to neurodegeneration, brain atrophy, and cognitive decline, and whether imaging measurements of brain iron accumulation using quantitative susceptibility mapping predicts subsequent brain atrophy and cognitive decline.

METHODS

A total of 440 subjects will be recruited for this study with 220 healthy subjects and 220 TIA patients. Early Alzheimer's pathology will be determined by cerebrospinal fluid samples (including tau, a marker of neuronal injury, and amyloid β) and by MR measurements of iron accumulation, a marker for Alzheimer's-related neurodegeneration. Small vessel disease will be identified by changes in white matter lesion volume. Predictors of advanced rates of cerebral and hippocampal atrophy at 1 and 3 years will include in vivo Alzheimer's disease pathology markers, and MRI measurements of brain iron accumulation and small vessel disease. Clinical and cognitive function will be assessed annually post-baseline for a period of 5-years using a clinical questionnaire and a battery of neuropsychological tests, respectively.

DISCUSSION

The PREVENT study expects to demonstrate that TIA patients have increased early progressive rates of cerebral brain atrophy after TIA, before cognitive decline can be clinically detected. By developing and optimizing high-level machine learning models based on clinical data, image-based (quantitative susceptibility mapping, regional brain, and white matter lesion volumes) features, and cerebrospinal fluid biomarkers, PREVENT will provide a timely opportunity to identify individuals at greatest risk of late-life cognitive decline early in the course of disease, supporting future therapeutic strategies for the promotion of healthy aging.

摘要

背景

由于神经元逐渐丧失导致脑萎缩,认知能力在出现症状前数年就开始下降,预计在未来 20 年内,加拿大的这种情况将增加一倍。在相当一部分病例中(50%),晚年认知障碍归因于中年时期的血管和生活方式相关风险因素,因此,如果能够更早地发现早期疾病,就有机会有效预防认知能力下降。短暂性脑缺血发作(TIA)患者通常会出现一定程度的认知障碍,痴呆风险增加 4 倍。在短暂性脑缺血发作的痴呆前神经影像学(PREVENT)研究中,我们将研究哪些疾病过程(即阿尔茨海默病与血管疾病)导致神经退行性变、脑萎缩和认知能力下降,以及使用定量磁化率映射测量脑内铁积累是否可以预测随后的脑萎缩和认知能力下降。

方法

这项研究共招募 440 名受试者,其中 220 名健康受试者和 220 名 TIA 患者。早期阿尔茨海默病病理学将通过脑脊液样本(包括 tau,神经元损伤的标志物,和淀粉样β)和铁积累的磁共振测量(阿尔茨海默病相关神经退行性变的标志物)来确定。小血管疾病将通过白质病变体积的变化来识别。在 1 年和 3 年时大脑和海马体萎缩的高级预测指标将包括体内阿尔茨海默病病理学标志物,以及脑铁积累和小血管疾病的 MRI 测量。临床和认知功能将分别通过临床问卷和神经心理学测试在基线后每年进行评估,为期 5 年。

讨论

PREVENT 研究预计将表明,TIA 后,在认知能力下降能够临床检测到之前,TIA 患者的大脑脑萎缩的早期进展速度就会加快。通过基于临床数据、基于图像(定量磁化率映射、脑区和白质病变体积)特征和脑脊液生物标志物开发和优化高级机器学习模型,PREVENT 将及时提供机会,在疾病早期识别出认知能力下降风险最大的个体,为促进健康老龄化的未来治疗策略提供支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5857/6048817/7805a1534ade/12877_2018_858_Fig1_HTML.jpg

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