Preliminary in-vivo evidence for regionally detectable bioenergetic alterations in the cerebellum of patients with MSAc is provided, while basal ganglia results, particularly in MSAp, require cautious interpretation because of the spatial-resolution limits of the present 31P-MRSI approach.
Abstract
Multiple system atrophy (MSA) is a severe neurodegenerative disorder with various underlying pathophysiological features. Mitochondrial dysfunction has been implied as a viable treatment target in patients with MSA. Yet, there is a lack of in-vivo studies examining regional metabolic differences between the Parkinsonian (MSAp) and the cerebellar (MSAc) subtype of MSA. Twenty-four patients with MSA (12 patients with MSAp and 12 patients with MSAc), 24 patients with Parkinson’s disease (PD), and 24 age- and sex-matched healthy controls (HCs) underwent clinical evaluations and multimodal neuroimaging, including 31P-MRSI targeting the basal ganglia and the cerebellum. Ratios of high-energy phosphorus-containing metabolites (HEPs) were compared between groups. Only patients with MSAc showed decreased HEP levels in the cerebellum. Conversely, no differences in basal ganglia HEP levels appeared between both MSA subtypes, patients with PD, or HCs. Our findings provide preliminary in-vivo evidence for regionally detectable bioenergetic alterations in the cerebellum of patients with MSAc, while basal ganglia results, particularly in MSAp, require cautious interpretation because of the spatial-resolution limits of the present 31P-MRSI approach.
Parkinson's disease (PD) and multiple system atrophy (MSA) are alpha-synuclein-related neurodegenerative disorders with overlapping motor and non-motor symptoms but distinct pathology, clinical management, and prognosis. Early differential diagnosis, particularly between PD and the parkinsonian subtype of MSA (MSA-P),...
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Disorders of consciousness (DoC) are characterised by marked reductions in cerebral glucose metabolism, but the specific cellular and neurochemical processes driving this impairment remain unclear. To elucidate these mechanisms, a multimodal imaging approach combining [18F]-fluorodeoxyglucose positron emission tomograp...
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It is suggested that PD is characterized by extensive disruption of cortical-cerebellar functional hierarchy, exceeding the relatively limited alterations observed in ET.
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Ultra-high-field MRS preliminary evidence for altered resting M1 GABAergic neurochemistry in mild-to-moderate PD supports the utility of 7T MRS for probing motor-cortical neurochemistry in PD.
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BACKGROUND
Multiple sclerosis (MS) is a disease characterised by progressive neurodegeneration and demyelination, manifesting as focal white matter lesions (WML) and extending into normal-appearing white matter (NAWM) and grey matter (NAGM). In this exploratory, hypothesis-generating study, we investigated regional neu...
Ibrahim Khormi, O. Al-iedani, Amir Fazlollahi et al.· Multiple Sclerosis and Relat...· 0 citations
ABSTRACT Background Apathy is a frequent nonmotor symptom of multiple system atrophy (MSA) that worsens quality of life. Although frontostriatal dysfunction has been implicated in apathy, its neural basis in MSA remains insufficiently characterized. Objectives To identify the neural substrates of apathy associated with...
Y. Nakagawa, A. Sugiyama, Yoshikazu Nakano et al.· European Journal of Neurolog...· 0 citations
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