Different Inflammatory Signatures in Alzheimer’s Disease and Frontotemporal Dementia Cerebrospinal Fluid

  • Gustaf Boström
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden
  • Eva Freyhult
    Department of Medical Sciences, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Johan Virhammar
    Department of Neuroscience, Neurology, Uppsala University Hospital, Uppsala, Sweden
  • Daniel Alcolea
    Memory Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
  • Hayrettin Tumani
    Department of Neurology, Ulm University Hospital, Ulm, Germany
  • Markus Otto
    Department of Neurology, Ulm University Hospital, Ulm, Germany
  • Rose-Marie Brundin
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden
  • Lena Kilander
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden
  • Malin Löwenmark
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden
  • Vilmantas Giedraitis
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden
  • Alberto Lleó
    Memory Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
  • Christine A.F. von Arnim
    Department of Neurology, Ulm University Hospital, Ulm, Germany
  • Kim Kultima
    Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden
  • Martin Ingelsson
    Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden

説明

<jats:p>Background: Neuroinflammatory processes are common in neurodegenerative diseases such as Alzheimer’s disease (AD) and frontotemporal dementia (FTD), but current knowledge is limited as to whether cerebrospinal fluid (CSF) levels of neuroinflammatory proteins are altered in these diseases. Objective: To identify and characterize neuroinflammatory signatures in CSF from patients with AD, mild cognitive impairment (MCI), and FTD. Methods: We used proximity extension assay and ANOVA to measure and compare levels of 92 inflammatory proteins in CSF from 42 patients with AD, 29 with MCI due to AD (MCI/AD), 22 with stable MCI, 42 with FTD, and 49 control subjects, correcting for age, gender, collection unit, and multiple testing. Results: Levels of matrix metalloproteinase-10 (MMP-10) were increased in AD, MCI/AD, and FTD compared with controls (AD: fold change [FC] = 1.32, 95% confidence interval [CI] 1.14–1.53, q = 0.018; MCI/AD: FC = 1.53, 95% CI 1.20–1.94, q = 0.045; and FTD: FC = 1.42, 95% CI 1.10–1.83, q = 0.020). MMP-10 and eleven additional proteins were increased in MCI/AD, compared with MCI (q < 0.05). In FTD, 36 proteins were decreased, while none was decreased in AD or MCI/AD, compared with controls (q < 0.05). Conclusion: In this cross-sectional multi-center study, we found distinct patterns of CSF inflammatory marker levels in FTD and in both early and established AD, suggesting differing neuroinflammatory processes in the two disorders.</jats:p>

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