Abstract
ObjectiveAlzheimer’s disease (AD) is a neurodegenerative disease characterized by progressive deterioration of memory and cognition. Mild cognitive impairment (MCI) has been implicated as a prodromal phase of AD. Although abnormal functional connectivity (FC) has been demonstrated in AD and MCI, the clinical differentiation of AD, MCI, and normal aging remains difficult, and the distinction between MCI and normal aging is especially problematic. We hypothesized that FC between the hippocampus and other brain structures is altered in AD and MCI, and that measurement of abnormal FC could have diagnostic utility for the classification of different AD stages.MethodsElderly adults aged 60–85 years were assigned to AD, MCI, or normal control (NC) groups based on clinical criteria. Functional magnetic resonance scanning was completed by 119 subjects. Five dimension reduction/classification methods were applied, using hippocampus-derived FC strengths as input features. Classification performance of the five dimensionality reduction methods was compared between AD, MCI, and NC groups.ResultsFCs between the hippocampus and left insula, left thalamus, cerebellum, right lingual gyrus, posterior cingulate cortex, and precuneus were significantly reduced in AD and MCI. Support vector machine learning coupled with sparse principal component analysis demonstrated the best discriminative performance, yielding classification accuracies of 82.02% (AD vs. NC), 81.33% (MCI vs. NC), and 81.08% (AD vs. MCI).ConclusionHippocampus-seed-based FCs were significantly different between AD, MCI, and NC groups. FC assessment combined with widely used machine learning methods can improve AD differential diagnosis, and may be especially useful to distinguish MCI from normal aging.
Highlights
Alzheimer’s disease (AD) is a progressive and irreversible neurodegenerative disease that leads to cognitive and physiologic dysfunction
Multiple lines of evidence suggest that AD and several psychiatric diseases are related to disruption or enhancement of functional connectivity (FC) (Bullmore and Sporns, 2009; Qiao et al, 2017)
Adults aged 60–85 years were assigned to AD, MCI, or normal control (NC) groups based on clinical criteria, and underwent functional MRI (fMRI) scanning
Summary
Alzheimer’s disease (AD) is a progressive and irreversible neurodegenerative disease that leads to cognitive and physiologic dysfunction. AD is idiopathic, and current therapies only alleviate symptoms or delay progression. Multiple lines of evidence suggest that AD and several psychiatric diseases are related to disruption or enhancement of FC (Bullmore and Sporns, 2009; Qiao et al, 2017). The efficacy of cognitive behavioral therapy for manic depressive disorder and post-traumatic stress disorder may result from strengthened FC between cortical centers of cognitive control and the amygdala, potentially enhancing topdown control of dysregulated affective processes (Shou et al, 2017). Most studies have focused narrowly on brain regions with abnormal connectivity, and have not further extracted the characteristics of these regional abnormalities to facilitate differential diagnosis. Relevant information encoded in abnormal connectivity could be used to improve clinical diagnosis and disease classification
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have