Cerebral peduncle angle: Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases

Philip W. Tipton, Takuya Konno, Daniel F. Broderick, Dennis W. Dickson, Zbigniew K. Wszolek

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)31-35
Number of pages5
JournalParkinsonism and Related Disorders
Volume32
DOIs
StatePublished - Nov 1 2016

Keywords

  • Cerebral peduncle angle
  • Corticobasal degeneration
  • Lewy body disease
  • Magnetic resonance imaging
  • Multiple system atrophy
  • Neurodegenerative diseases
  • PSP-Richardson Syndrome
  • Parkinson's disease

ASJC Scopus subject areas

  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology

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