Evaluation of an optimized [18F]fluoro‐deoxy‐glucose positron emission tomography voxel‐wise method to early support differential diagnosis in atypical Parkinsonian disorders

• Published in: European journal of neurology Vol. 24; no. 5; pp. 687 - e26
• Main Authors: Caminiti, S. P., Alongi, P., Majno, L., Volontè, M. A., Cerami, C., Gianolli, L., Comi, G., Perani, D.
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.05.2017
• Subjects: Accuracy; Aged; Aged, 80 and over; Basal Ganglia Diseases - diagnostic imaging; Basal Ganglia Diseases - metabolism; biomarkers; corticobasal degeneration; dementia with Lewy bodies; Diagnosis, Differential; Female; Fluorodeoxyglucose F18; Follow-Up Studies; Glucose; Humans; hypometabolism; Male; Middle Aged; multiple system atrophy; Neurodegenerative Diseases - diagnostic imaging; Neurodegenerative Diseases - metabolism; Parkinsonian Disorders - diagnostic imaging; Parkinsonian Disorders - metabolism; Positron-Emission Tomography - methods; progressive supranuclear palsy; Radiopharmaceuticals; Retrospective Studies; Sensitivity and Specificity; single subject; Statistical Parametric Mapping; Tomography; Statistical Parametric Mapping; dementia with Lewy bodies; corticobasal degeneration; hypometabolism; biomarkers; single subject; multiple system atrophy; progressive supranuclear palsy
• ISSN: 1351-5101; 1468-1331
• DOI: 10.1111/ene.13269

Background and purpose Atypical Parkinsonian disorders (APD) frequently overlap in clinical presentations, making the differential diagnosis challenging in the early stages. The present study aimed to evaluate the accuracy of the [18F]fluoro‐deoxy‐glucose positron emission tomography Statistical Parametric Mapping (SPM) optimized procedure in supporting the early and differential diagnosis of APD. Methods Seventy patients with possible APD were retrospectively included from a large clinical cohort. The included patients underwent [18F]fluoro‐deoxy‐glucose positron emission tomography within 3 months of the first clinical assessment and a diagnostic follow‐up. An optimized SPM voxel‐wise procedure was used to produce t‐maps of brain hypometabolism in single subjects, which were classified by experts blinded to any clinical information. We compared the accuracy of both the first clinical diagnosis and the SPM t‐map classifications with the diagnosis at follow‐up as the reference standard. Results At first diagnosis, 60% of patients were classified as possible APD (progressive supranuclear palsy, corticobasal degeneration, dementia with Lewy bodies, multiple system atrophy) and about 40% as APD with uncertain diagnosis, providing 52% sensitivity, 97% specificity and 86% accuracy with respect to the reference standard. SPM t‐map classification showed 98% sensitivity, 99% specificity and 99% accuracy, and a significant agreement with the diagnosis at follow‐up (P < 0.001). Conclusions The SPM t‐map classification at entry predicted the second diagnosis at follow‐up. This indicates its significantly superior role for an early identification of APD subtypes, particularly in cases of uncertain diagnosis. The use of a metabolic biomarker at entry in the instrumental work‐up of APD may shorten the diagnostic time, producing benefits for treatment options and support to the patients.