Differentiation between Parkinson’s Disease and the Parkinsonian Subtype of Multiple System Atrophy Using the Magnetic Resonance T1w/T2w Ratio in the Middle Cerebellar Peduncle

Author:

Wang Jiaqi1ORCID,Sugiyama Atsuhiko1ORCID,Yokota Hajime2,Hirano Shigeki1,Yamamoto Tatsuya13ORCID,Yamanaka Yoshitaka14,Araki Nobuyuki1,Ito Shoichi15ORCID,Paul Friedemann6789,Kuwabara Satoshi1

Affiliation:

1. Department of Neurology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan

2. Diagnostic Radiology and Radiation Oncology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan

3. Department of Rehabilitation, Division of Occupational Therapy, Chiba Prefectural University of Health Sciences, Chiba 261-0014, Japan

4. Urayasu Rehabilitation Education Center, Chiba University Hospital, Urayasu 279-0023, Japan

5. Department of Medical Education, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan

6. Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine and Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany

7. NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany

8. Einstein Center for Neurosciences, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany

9. Department of Neurology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany

Abstract

Multiple system atrophy with predominant parkinsonism (MSA-P) can hardly be distinguished from Parkinson’s disease (PD) clinically in the early stages. This study investigated whether a standardized T1-weighted/T2-weighted ratio (sT1w/T2w ratio) can effectively detect degenerative changes in the middle cerebellar peduncle (MCP) associated with MSA-P and PD and evaluated its potential to distinguish between these two diseases. We included 35 patients with MSA-P, 32 patients with PD, and 17 controls. T1w and T2w scans were acquired using a 1.5-T MR system. The MCP sT1w/T2w ratio was analyzed via SPM12 using a region-of-interest approach in a normalized space. The diagnostic performance of the MCP sT1w/T2w ratio was compared between the MSA-P, PD, and controls. Patients with MSA-P had significantly lower MCP sT1w/T2w ratios than patients with PD and controls. Furthermore, MCP sT1w/T2w ratios were lower in patients with PD than in the controls. The MCP sT1w/T2w ratio showed excellent or good accuracy for differentiating MSA-P or PD from the control (area under the curve (AUC) = 0.919 and 0.814, respectively) and substantial power for differentiating MSA-P from PD (AUC = 0.724). Therefore, the MCP sT1w/T2w ratio is sensitive in detecting degenerative changes in the MCP associated with MSA-P and PD and is useful in distinguishing MSA-P from PD.

Funder

Grants-in-Aid from the Research Committee of Ataxia, the Health Labor Sciences Research Grant, and the Ministry of Health, Labor and Welfare, Japan

Publisher

MDPI AG

Subject

Clinical Biochemistry

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