Patterns of gray matter atrophy in atypical parkinsonism syndromes: a VBM meta‐analysis. Issue 6 (11th March 2015)

• Record Type: Journal Article
• Authors: Yu, Fang; Barron, Daniel S.; Tantiwongkosi, Bundhit; Fox, Peter
• Is Part Of: Brain and behavior. Volume 5:Issue 6(2015:Jun.)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2015-03-11
• Subjects: Neurology -- Periodicals; Neurosciences -- Periodicals; Psychology -- Periodicals; Psychiatry -- Periodicals; 616.8005
• DOI: 10.1002/brb3.329
• Languages: English
• ISSNs: 2162-3279

Abstract

<abstract abstract-type="main" id="brb3329-abs-0001"> <title>Abstract</title> <sec id="brb3329-sec-0001" sec-type="section"> <title>Background and Purpose</title> <p>Accurate diagnosis of Atypical Parkinsonian Syndromes (APS) is important due to differences in prognosis and management, but remains a challenge in the clinical setting. The purpose of our meta‐analysis was to identify characteristic patterns of gray matter atrophy in Corticobasal Degeneration (CBD), Progressive Supranuclear Palsy (PSP), Multisystem‐Atrophy Parkinsonian type (MSA‐P), and Idiopathic Parkinson's Disease (IPD).</p> </sec> <sec id="brb3329-sec-0002" sec-type="section"> <title>Materials and Methods</title> <p>Whole‐brain meta‐analysis was performed on 39 published voxel‐based morphometry (VBM) articles (consisting of 404 IPD, 87 MSA‐P, 165 CBD, and 176 PSP subjects) using the modified Anatomic Likelihood Estimation method. Based on these results, contrast analyses were then utilized to determine areas of atrophy shared by as well as unique to each disorder.</p> </sec> <sec id="brb3329-sec-0003" sec-type="section"> <title>Results</title> <p>CBD was characterized by asymmetric gray matter atrophy in multiple cortical regions, while the thalamus‐midbrain and insula were predominantly involved in PSP. The striatum and superior cerebellum were affected in MSA‐P, while IPD demonstrated an anterior cerebral pattern. Although there was a mild overlap among PSP, CBD, and MSA‐P, significant regions of atrophy unique to each disorder were identified, including (1) the superior parietal lobule in CBD (2) putamen in MSA‐P (3) insula and medial dorsal nucleus in PSP.</p> </sec> <sec id="brb3329-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Our results suggest that there are characteristic patterns of atrophy in APS. Guided by these findings, future studies on the individual subject level may lead to the development of robust imaging biomarkers.</p> </sec> </abstract>