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Cognitive function in very old men does not correlate to biomarkers of Alzheimer's disease.
Velickaite, V; Giedraitis, V; Ström, K; Alafuzoff, I; Zetterberg, H; Lannfelt, L; Kilander, L; Larsson, E-M; Ingelsson, M.
Afiliação
  • Velickaite V; Department of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden.
  • Giedraitis V; Department of Public Health and Caring Sciences/Geriatrics, Uppsala University, Uppsala, Sweden.
  • Ström K; Department of Public Health and Caring Sciences/Geriatrics, Uppsala University, Uppsala, Sweden.
  • Alafuzoff I; Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
  • Zetterberg H; Department of Pathology Uppsala University Hospital, Uppsala, Sweden.
  • Lannfelt L; Department of Psychiatry and Neurochemistry, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Kilander L; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Larsson EM; Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.
  • Ingelsson M; Department of Public Health and Caring Sciences/Geriatrics, Uppsala University, Uppsala, Sweden.
BMC Geriatr ; 17(1): 208, 2017 09 08.
Article em En | MEDLINE | ID: mdl-28886705
ABSTRACT

BACKGROUND:

The Alzheimer's disease (AD) brain displays atrophy with amyloid-ß (Aß) and tau deposition, whereas decreased Aß42 and increased tau are measured in cerebrospinal fluid (CSF). The aim of this study was to relate cognitive performance to the degree of brain atrophy, CSF biomarker levels and neuropathology in a cohort of aged men.

METHODS:

Fifty-eight 86-92-year-old men from the Uppsala Longitudinal Study of Adult Men (ULSAM) cohort underwent cognitive testing, brain computed tomography and lumbar puncture. Atrophy was graded with established scales. Concentrations of CSF Aß42, t-tau and p-tau were measured by ELISA. Thirteen brains were examined post mortem.

RESULTS:

Forty-six of the individuals were considered non-demented, whereas twelve were diagnosed with dementia, either at baseline (n = 4) or during follow-up (n = 8). When comparing subjects with and without dementia, there were no differences in the degree of atrophy, although the mini mental state examination (MMSE) scoring correlated weakly with the degree of medial temporal atrophy (MTA) (p = 0.04). Moreover, the CSF biomarker levels did not differ significantly between healthy (n = 27) and demented (n = 8) subjects (median values 715 vs 472 pg/ml for Aß42, 414 vs 427 pg/ml for t-tau and 63 vs 60 pg/ml for p-tau). Similarly, there were no differences in the biomarker levels between individuals with mild (n = 24) and severe (n = 11) MTA (median values 643 vs 715 pg/ml for Aß42, 441 vs 401 pg/ml for t-tau and 64 vs 53 pg/ml for p-tau). Finally, the neuropathological changes did not correlate with any of the other measures.

CONCLUSION:

In this cohort of aged men only a weak correlation could be seen between cognitive performance and MTA, whereas the various neuroradiological, biochemical and neuropathological measures did not correlate with each other. Thus, AD biomarkers seem to be less informative in subjects of an advanced age.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Peptídeos beta-Amiloides / Proteínas tau / Cognição / Doença de Alzheimer Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Peptídeos beta-Amiloides / Proteínas tau / Cognição / Doença de Alzheimer Idioma: En Ano de publicação: 2017 Tipo de documento: Article