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         headline:Clinical validity of Braak neuropathological staging in the oldest-old
         description: Several studies have demonstrated a good correlation between clinical severity and Braak’s neuropathological staging in Alzheimer’s disease (AD). However, nonagenarians and centenarians display a different pattern of cortical vulnerability to the neurodegenerative process compared to younger elderly, and it is not known whether correlations between clinical severity and neuropathological stages remain valid in this age group. To address this issue we compared Clinical Dementia Rating scale (CDR) scores and Braak stages in 116 patients over 90 years of age with either no cognitive impairment or very mild to severe AD. There is a strong positive correlation between CDR scores and Braak staging (Spearman coefficient = 0.66; P < 0.01). However, neuropathological staging does not distinguish cases with normal cognition (CDR 0) from those with mild cognitive changes (CDR 0.5). Unlike younger cohorts, Braak stages I and II are frequently associated with questionable dementia in this age group. Braak stage III overlaps with all CDR levels and correlates poorly with cognitive function. Braak stages IV or greater are consistently associated with at least mild dementia. Consistent with our previous neuropathological analyses of nonagenarians and centenarians, the present data suggest that the substantial involvement of the hippocampus which characterizes Braak stage IV is a key step in the development of overt clinical signs of dementia in the oldest-old. Moreover, they indicate that Braak staging represents a broad concept of the evolution of neurofibrillary tangles rather than a precise hierarchical model associated with a stepwise deterioration of cognitive abilities near the upper limit of life.
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            Key words Alzheimer’s disease
            Clinicopathological correlations
            Cognitive impairment
            dementia
            Neurofibrillary tangles
            Pathology
            Neurosciences
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                        name:Department of Geriatrics, University Hospitals of Geneva, 1226 Thônex-Genève, Switzerland e-mail: [email protected], Tel.: +41-22-3056535, Fax: +41-22-3056115, , CH
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      headline:Clinical validity of Braak neuropathological staging in the oldest-old
      description: Several studies have demonstrated a good correlation between clinical severity and Braak’s neuropathological staging in Alzheimer’s disease (AD). However, nonagenarians and centenarians display a different pattern of cortical vulnerability to the neurodegenerative process compared to younger elderly, and it is not known whether correlations between clinical severity and neuropathological stages remain valid in this age group. To address this issue we compared Clinical Dementia Rating scale (CDR) scores and Braak stages in 116 patients over 90 years of age with either no cognitive impairment or very mild to severe AD. There is a strong positive correlation between CDR scores and Braak staging (Spearman coefficient = 0.66; P < 0.01). However, neuropathological staging does not distinguish cases with normal cognition (CDR 0) from those with mild cognitive changes (CDR 0.5). Unlike younger cohorts, Braak stages I and II are frequently associated with questionable dementia in this age group. Braak stage III overlaps with all CDR levels and correlates poorly with cognitive function. Braak stages IV or greater are consistently associated with at least mild dementia. Consistent with our previous neuropathological analyses of nonagenarians and centenarians, the present data suggest that the substantial involvement of the hippocampus which characterizes Braak stage IV is a key step in the development of overt clinical signs of dementia in the oldest-old. Moreover, they indicate that Braak staging represents a broad concept of the evolution of neurofibrillary tangles rather than a precise hierarchical model associated with a stepwise deterioration of cognitive abilities near the upper limit of life.
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      dateModified:
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      pageEnd:582
      sameAs:https://doi.org/10.1007/s004010051163
      keywords:
         Key words Alzheimer’s disease
         Clinicopathological correlations
         Cognitive impairment
         dementia
         Neurofibrillary tangles
         Pathology
         Neurosciences
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                  address:
                     name:Department of Geriatrics, University Hospitals of Geneva, 1226 Thônex-Genève, Switzerland e-mail: [email protected], Tel.: +41-22-3056535, Fax: +41-22-3056115, , CH
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            name:E. Kövari
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                     name:Department of Geriatrics, University Hospitals of Geneva, 1226 Thônex-Genève, Switzerland e-mail: [email protected], Tel.: +41-22-3056535, Fax: +41-22-3056115, , CH
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               name:Department of Geriatrics, University Hospitals of Geneva, 1226 Thônex-Genève, Switzerland e-mail: [email protected], Tel.: +41-22-3056535, Fax: +41-22-3056115, , CH
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