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Updated: May 1, 2026

Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
The value of novel MRI techniques in Parkinson-plus syndromes: diffusion tensor imaging and anatomical connectivity
M Tir1, C Delmaire2, P Besson2
1Service de neurologie et pathologie du mouvement, hôpital Salengro, CHRU de Lille, EA 1046, département de pharmacologie médicale, université Lille Nord de France, 1, place de Verdun, 59045 Lille cedex, France; Service de neurologie, CHU d'Amiens, EA 4559, SFR CAP-Santé (FED 4231), université de Picardie-Jules-Verne, chemin du Thil, 80000 Amiens, France.
Abstract:
Conventional MRI is a well-described, highly useful tool for the differential diagnosis of degenerative parkinsonian syndromes. Nevertheless, the observed abnormalities may only appear in late-stage disease. Diffusion tensor imaging (DTI) can identify microstructural changes in brain tissue integrity and connectivity. The technique has proven value in the differential diagnosis of multiple system atrophy (MSA), progressive supranuclear palsy (PSP) and Parkinson's disease (PD). Here, we performed a systematic review of the literature on the main corticosubcortical DTI abnormalities identified to date in the context of the diagnosis of MSA and PSP with diffusion-weighted imaging, diffusion tensor imaging and anatomical connectivity studies. In good agreement with the histological data, increased diffusivity in the putamen (in MSA and PSP), in the middle cerebellar peduncles (in MSA) and in the upper cerebellar peduncles (in PSP) has been reported. Motor pathway involvement is characterized by low fraction anisotropy (FA) in the primary motor cortex in MSA-P and PSP, a high apparent diffusion coefficient (ADC) and low FA in the supplementary motor area in PSP. We then outline the value of these techniques in differential diagnosis (especially with respect to PD). Anatomical connectivity studies have revealed a lower number of fibers in the corticospinal tract in MSA and PSP (relative to PD and controls) and fewer tracked cortical projection fibers in patients with PSP or late-stage MSA (relative to patients with early MSA or PD and controls). Lastly, we report the main literature data concerning the value of DTI parameters in monitoring disease progression. The observed correlations between DTI parameters on one hand and clinical scores and/or disease duration on the other constitute strong evidence of the value of DTI in monitoring disease progression. In MSA, the ataxia score was correlated with ADC values in the pons and the upper cerebellar peduncles, whereas both the motor score and the disease duration were correlated with putaminal ADC values. In conclusion, DTI and connectivity studies constitute promising tools for differentiating between "Parkinson-plus" syndromes.
Insights
Diffusion tensor imaging (DTI) reveals microstructural brain changes, aiding in differentiating Parkinson-plus syndromes like MSA and PSP from Parkinson's disease. DTI parameters also show promise for monitoring disease progression.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Conventional MRI has limitations in early differential diagnosis of degenerative parkinsonian syndromes.
- Diffusion Tensor Imaging (DTI) detects microstructural brain tissue changes and connectivity alterations.
- DTI shows potential in distinguishing Multiple System Atrophy (MSA), Progressive Supranuclear Palsy (PSP), and Parkinson's Disease (PD).
Purpose of the Study:
- To systematically review corticosubcortical DTI abnormalities in MSA and PSP.
- To assess the diagnostic value of DTI and connectivity studies in differentiating Parkinson-plus syndromes.
- To explore the utility of DTI parameters in monitoring disease progression.
Main Methods:
- Systematic literature review of diffusion-weighted imaging, DTI, and anatomical connectivity studies.
- Analysis of DTI abnormalities in specific brain regions (putamen, cerebellar peduncles, motor cortex).
- Correlation of DTI parameters with clinical scores and disease duration.
Main Results:
- Increased diffusivity observed in the putamen (MSA, PSP), middle cerebellar peduncles (MSA), and upper cerebellar peduncles (PSP).
- Reduced fractional anisotropy (FA) in motor pathways and increased apparent diffusion coefficient (ADC) in supplementary motor area noted in PSP.
- Anatomical connectivity studies revealed reduced corticospinal tract fibers in MSA and PSP.
- Correlations between DTI parameters and clinical scores/disease duration indicate value in monitoring progression.
Conclusions:
- DTI and connectivity studies are valuable tools for differentiating between MSA and PSP.
- These techniques offer advantages over conventional MRI, especially in early disease stages.
- DTI parameters show significant potential for tracking disease progression in degenerative parkinsonian syndromes.
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