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Intrinsic Functional Component Analysis via Sparse Representation on Alzheimers Disease Neuroimaging Initiative Database

机译:通过稀疏表示在阿尔茨海默氏病神经成像计划数据库中进行内在功能成分分析

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摘要

Alzheimer's disease (AD) is the most common type of dementia (accounting for 60% to 80%) and is the fifth leading cause of death for those people who are 65 or older. By 2050, one new case of AD in United States is expected to develop every 33 sec. Unfortunately, there is no available effective treatment that can stop or slow the death of neurons that causes AD symptoms. On the other hand, it is widely believed that AD starts before development of the associated symptoms, so its prestages, including mild cognitive impairment (MCI) or even significant memory concern (SMC), have received increasing attention, not only because of their potential as a precursor of AD, but also as a possible predictor of conversion to other neurodegenerative diseases. Although these prestages have been defined clinically, accurate/efficient diagnosis is still challenging. Moreover, brain functional abnormalities behind those alterations and conversions are still unclear. In this article, by developing novel sparse representations of whole-brain resting-state functional magnetic resonance imaging signals and by using the most updated Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset, we successfully identified multiple functional components simultaneously, and which potentially represent those intrinsic functional networks involved in the resting-state activities. Interestingly, these identified functional components contain all the resting-state networks obtained from traditional independent-component analysis. Moreover, by using the features derived from those functional components, it yields high classification accuracy for both AD (94%) and MCI (92%) versus normal controls. Even for SMC we can still have 92% accuracy.
机译:阿尔茨海默氏病(AD)是最常见的痴呆类型(占60%至80%),并且是65岁以上老年人的第五大死亡原因。到2050年,预计美国每33微秒就会出现一例新的AD。不幸的是,没有可用的有效治疗方法可以阻止或减慢引起AD症状的神经元的死亡。另一方面,人们普遍认为,AD在相关症状出现之前就已开始,因此它的前期阶段,包括轻度认知障碍(MCI)甚至显着的记忆障碍(SMC),都受到了越来越多的关注,不仅仅是因为它们具有潜在的优势。作为AD的前体,但也可能是转化为其他神经退行性疾病的可能指标。尽管已经对这些前期进行了临床定义,但准确/有效的诊断仍具有挑战性。此外,这些改变和转换背后的脑功能异常仍不清楚。在本文中,通过开发全脑静止状态功能磁共振成像信号的新颖稀疏表示形式,并使用最新的阿尔茨海默氏病神经成像计划(ADNI)数据集,我们成功地同时识别了多个功能组件,并且潜在地代表了那些内在的功能组件参与静止状态活动的功能网络。有趣的是,这些确定的功能组件包含从传统独立组件分析中获得的所有静止状态网络。此外,通过使用衍生自那些功能组件的功能,与正常对照相比,AD(94%)和MCI(92%)均具有很高的分类精度。即使对于SMC,我们仍然可以达到92%的精度。

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