4.5 Article

Neuropathological findings of PSP in the elderly without clinical PSP: Possible incidental PSP?

期刊

PARKINSONISM & RELATED DISORDERS
卷 17, 期 5, 页码 365-371

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2011.02.017

关键词

Progressive supranuclear palsy; PSP; Incidental; Autopsy; Parkinsonism; Neuropathology

资金

  1. National Institute of Aging [P30 AG19610]
  2. Arizona Department of Health Services [211002]
  3. Arizona Biomedical Research Commission [4001, 0011, 05-901]
  4. Prescott Family Initiative of the Michael J. Fox Foundation for Parkinson's Research

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Aims: We aimed to describe cases with incidental neuropathological findings of progressive supranuclear palsy (PSP) from the Banner Sun Health Research Institute Brain and Body Donation Program. Methods: We performed a retrospective review of 277 subjects with longitudinal motor and neuropsychological assessments who came to autopsy. The mean Gallyas-positive PSP features grading for subjects with possible incidental neuropathological PSP was compared to those of subjects with clinically manifest disease. Results: There were 5 cases with histopathological findings suggestive of PSP, but no parkinsonism, dementia or movement disorder during life. Cognitive evaluation revealed 4 of the 5 cases to be cognitively normal; one case had amnestic mild cognitive impairment (MCI) in her last year of life. The mean age at death of the 5 cases was 88.9 years (range 80-94). All 5 individuals had histopathologic microscopic findings suggestive of PSP Mean Gallyas-positive PSP features grading was significantly lower in subjects with possible incidental neuropathological PSP than subjects with clinical PSP, particularly in the subthalamic nucleus. Conclusions: We present 5 patients with histopathological findings suggestive of PSP, without clinical PSP, dementia or parkinsonism during life. These incidental neuropathological PSP findings may represent the early or pre-symptomatic stage of PSP. The mean Gallyas-positive PSP features grading was significantly lower in possible incidental PSP than in clinical PSP, thus suggesting that a threshold of pathological burden needs to be reached within the typically affected areas in PSP before clinical signs and symptoms appear. (C) 2011 Elsevier Ltd. All rights reserved.

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