TY - JOUR
T1 - Cerebral peduncle angle
T2 - Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases
AU - Tipton, Philip W.
AU - Konno, Takuya
AU - Broderick, Daniel F.
AU - Dickson, Dennis W.
AU - Wszolek, Zbigniew K.
N1 - Funding Information:
P. Tipton reports no disclosures relevant to the manuscript. T. Konno received research support from the JSPS Postdoctoral Fellowship for Research Abroad and is partially supported by the gift from Carl Edward Bolch, Jr., and Susan Bass Bolch. D. Broderick reports no disclosures relevant to the manuscript. D. Dickson is supported by the NIH P50 NS072187 , P50 AG16574 , The Robert E. Jacoby Professorship in Alzheimer's Research and the Mangurian Foundation Lewy Body Dementia program at Mayo Clinic. Z. Wszolek is supported by the NIH P50 NS072187 , Mayo Clinic Center for Regenerative Medicine , Mayo Clinic Center for Individualized Medicine , Mayo Clinic Neuroscience Focused Research Team (Cecilia and Dan Carmichael Family Foundation, and the James C. and Sarah K. Kennedy Fund for Neurodegenerative Disease Research at Mayo Clinic in Florida), and The Sol Goldman Charitable Trust .
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Introduction The significant symptom overlap between progressive supranuclear palsy (PSP) and other parkinsonian neurodegenerative diseases frequently results in misdiagnosis. However, neuroimaging can be used to quantify disease-related morphological changes and specific markers. The cerebral peduncle angle (CPA) has been shown to differentiate clinically diagnosed PSP from other parkinsonian diseases but this result has yet to be confirmed in autopsy-proven disease. Methods Magnetic resonance imaging (MRI) scans were obtained for 168 patients representing 69 medical facilities. Following randomization, the images were divided into two groups (Type 1 and Type 2) based upon midbrain morphological differences. Two readers were blinded and independently measured the CPA of 146 patients with autopsy-proven progressive supranuclear palsy (PSP; n = 54), corticobasal degeneration (n = 16), multiple system atrophy (MSA; n = 11) and Lewy body disease (n = 65). Results Applying two separate measurement techniques revealed no statistically significant differences in CPA measurements among any study groups regardless of classification measurement approach. The interobserver agreement showed significant differences in measurements using the Type 2 approach. Conclusion Measuring the CPA on MRI is not a reliable way of differentiating among patients with PSP, corticobasal degeneration, MSA, or Lewy body disease.
AB - Introduction The significant symptom overlap between progressive supranuclear palsy (PSP) and other parkinsonian neurodegenerative diseases frequently results in misdiagnosis. However, neuroimaging can be used to quantify disease-related morphological changes and specific markers. The cerebral peduncle angle (CPA) has been shown to differentiate clinically diagnosed PSP from other parkinsonian diseases but this result has yet to be confirmed in autopsy-proven disease. Methods Magnetic resonance imaging (MRI) scans were obtained for 168 patients representing 69 medical facilities. Following randomization, the images were divided into two groups (Type 1 and Type 2) based upon midbrain morphological differences. Two readers were blinded and independently measured the CPA of 146 patients with autopsy-proven progressive supranuclear palsy (PSP; n = 54), corticobasal degeneration (n = 16), multiple system atrophy (MSA; n = 11) and Lewy body disease (n = 65). Results Applying two separate measurement techniques revealed no statistically significant differences in CPA measurements among any study groups regardless of classification measurement approach. The interobserver agreement showed significant differences in measurements using the Type 2 approach. Conclusion Measuring the CPA on MRI is not a reliable way of differentiating among patients with PSP, corticobasal degeneration, MSA, or Lewy body disease.
KW - Cerebral peduncle angle
KW - Corticobasal degeneration
KW - Lewy body disease
KW - Magnetic resonance imaging
KW - Multiple system atrophy
KW - Neurodegenerative diseases
KW - PSP-Richardson Syndrome
KW - Parkinson's disease
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U2 - 10.1016/j.parkreldis.2016.08.009
DO - 10.1016/j.parkreldis.2016.08.009
M3 - Article
C2 - 27553513
AN - SCOPUS:84994704800
SN - 1353-8020
VL - 32
SP - 31
EP - 35
JO - Parkinsonism and Related Disorders
JF - Parkinsonism and Related Disorders
ER -