Alzheimer’s Disease-Related Metabolic Pattern in Diverse Forms of Neurodegenerative Diseases

• Published in: Diagnostics (Basel) Vol. 11; no. 11; p. 2023
• Main Authors: Lau, Angus, Beheshti, Iman, Modirrousta, Mandana, Kolesar, Tiffany A., Goertzen, Andrew L., Ko, Ji Hyun
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2021; MDPI
• Subjects: Age; Algorithms; Alzheimer's disease; Aphasia; Biomarkers; Brain research; Dementia; FDG-PET; machine learning; Medical imaging; Mental disorders; metabolic classification; Metabolism; neurodegenerative disease; Parkinson's disease; Patients; Proteins; support vector machine
• ISSN: 2075-4418; 2075-4418
• DOI: 10.3390/diagnostics11112023

Dementia is broadly characterized by cognitive and psychological dysfunction that significantly impairs daily functioning. Dementia has many causes including Alzheimer’s disease (AD), dementia with Lewy bodies (DLB), and frontotemporal lobar degeneration (FTLD). Detection and differential diagnosis in the early stages of dementia remains challenging. Fueled by AD Neuroimaging Initiatives (ADNI) (Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. As such, the investigators within ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report.), a number of neuroimaging biomarkers for AD have been proposed, yet it remains to be seen whether these markers are also sensitive to other types of dementia. We assessed AD-related metabolic patterns in 27 patients with diverse forms of dementia (five had probable/possible AD while others had atypical cases) and 20 non-demented individuals. All participants had positron emission tomography (PET) scans on file. We used a pre-trained machine learning-based AD designation (MAD) framework to investigate the AD-related metabolic pattern among the participants under study. The MAD algorithm showed a sensitivity of 0.67 and specificity of 0.90 for distinguishing dementia patients from non-dementia participants. A total of 18/27 dementia patients and 2/20 non-dementia patients were identified as having AD-like patterns of metabolism. These results highlight that many underlying causes of dementia have similar hypometabolic pattern as AD and this similarity is an interesting avenue for future research.