BACKGROUND: The cerebrospinal fluid (CSF) proteins beta-amyloid 42 (Abeta42) and Tau are believed to indirectly reflect some core pathological features of Alzheimer's disease (AD). Their topographic origin and their association with synaptic dysfunction are still not well understood. AIM: The present study aimed to explore possible associations between cerebral glucose metabolism and CSF Abeta42 as well as Tau protein levels in AD. METHODS: CSF analyses and (18)F-FDG PET scans were conducted on 32 patients with mild-to-moderate AD. Voxel-based statistical parametric correlations were computed for CSF protein levels and cerebral glucose metabolism. RESULTS: After correction for multiple comparisons, a strong positive association between CSF Abeta42 levels and glucose metabolism was identified for 2 extensive clusters located in the right temporal, prefrontal and anterior cingulate cortices. For CSF Tau protein, no association was observed for any brain region. CONCLUSIONS: These findings point to a significant association between synaptic dysfunction as measured with (18)F-FDG PET and CSF Abeta42 levels, but do not suggest a correlation between synaptic function and CSF Tau levels.
BACKGROUND: The cerebrospinal fluid (CSF) proteins beta-amyloid 42 (Abeta42) and Tau are believed to indirectly reflect some core pathological features of Alzheimer's disease (AD). Their topographic origin and their association with synaptic dysfunction are still not well understood. AIM: The present study aimed to explore possible associations between cerebral glucose metabolism and CSF Abeta42 as well as Tau protein levels in AD. METHODS: CSF analyses and (18)F-FDG PET scans were conducted on 32 patients with mild-to-moderate AD. Voxel-based statistical parametric correlations were computed for CSF protein levels and cerebral glucose metabolism. RESULTS: After correction for multiple comparisons, a strong positive association between CSF Abeta42 levels and glucose metabolism was identified for 2 extensive clusters located in the right temporal, prefrontal and anterior cingulate cortices. For CSF Tau protein, no association was observed for any brain region. CONCLUSIONS: These findings point to a significant association between synaptic dysfunction as measured with (18)F-FDG PET and CSF Abeta42 levels, but do not suggest a correlation between synaptic function and CSF Tau levels.
Authors: Ina S Almdahl; Camilla Lauridsen; Per Selnes; Lisa F Kalheim; Christopher Coello; Beata Gajdzik; Ina Møller; Marianne Wettergreen; Ramune Grambaite; Atle Bjørnerud; Geir Bråthen; Sigrid B Sando; Linda R White; Tormod Fladby Journal: Front Aging Neurosci Date: 2017-02-07 Impact factor: 5.750
Authors: Stefan L C Geijselaers; Pauline Aalten; Inez H G B Ramakers; Peter Paul De Deyn; Annemieke C Heijboer; Huiberdina L Koek; Marcel G M OldeRikkert; Janne M Papma; Fransje E Reesink; Lieke L Smits; Coen D A Stehouwer; Charlotte E Teunissen; Frans R J Verhey; Wiesje M van der Flier; Geert Jan Biessels Journal: J Alzheimers Dis Date: 2018 Impact factor: 4.472