| Literature DB >> 32147244 |
Dejan Jakimovski1, Niels Bergsland2, Michael G Dwyer1, Jesper Hagemeier1, Deepa P Ramasamy1, Kinga Szigeti3, Thomas Guttuso3, David Lichter3, David Hojnacki4, Bianca Weinstock-Guttman4, Ralph H B Benedict4, Robert Zivadinov5.
Abstract
Multiple sclerosis (MS) exhibits neurodegeneration driven disability progression. We compared the extent of neurodegeneration among 112 long-standing MS patients, 37 Parkinson's disease (PD) patients, 34 amnestic mild cognitive impairment (aMCI) patients, 37 Alzheimer's disease (AD) patients, and 184 healthy controls. 3T MRI volumes of whole brain (WBV), white matter (WMV), gray matter (GMV), cortical (CV), deep gray matter (DGM), and nuclei-specific volumes of thalamus, caudate, putamen, globus pallidus, and hippocampus were derived with SIENAX and FIRST software. Аge and sex-adjusted analysis of covariance was used. WBV was not significantly different between diseases. MS had significantly lower WMV compared to other disease groups (p < 0.021). Only AD had smaller GMV and CV when compared to MS (both p < 0.001). MS had smaller DGM volume than PD and aMCI (p < 0.001 and p = 0.026, respectively) and lower thalamic volume when compared to all other neurodegenerative diseases (p < 0.008). Long-standing MS exhibits comparable global atrophy with lower WMV and thalamic volume when compared to other classical neurodegenerative diseases.Entities:
Keywords: Alzheimer’s disease; Deep gray matter; MRI; Multiple sclerosis; Neurodegeneration; Parkinson’s disease; Thalamus; Whole brain atrophy
Mesh:
Year: 2020 PMID: 32147244 PMCID: PMC7166193 DOI: 10.1016/j.neurobiolaging.2020.02.002
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673