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CSF α-synuclein correlates with CSF neurogranin in late-life depression.

Davide BrunoChelsea Reichert PlaskaDaniel P A ClarkHenrik ZetterbergKaj BlennowMarcel M VerbeekNunzio Pomara
Published in: The International journal of neuroscience (2020)
Purpose/aim of the study: Major depressive disorder (MDD) in late life is linked to increased risk of subsequent dementia, but it is still unclear exactly what pathophysiological mechanisms underpin this link. A potential mechanism related to elevated risk of dementia in MDD is increased levels of α-synuclein (α-Syn), a protein found in presynaptic neuronal terminals.Materials and methods: In this study, we examined cerebrospinal fluid (CSF) levels of α-Syn in conjunction with biomarkers of neurodegeneration (amyloid-β 42, total and phospho tau) and synaptic dysfunction (neurogranin), and measures of memory ability, in 27 cognitively intact older individuals with MDD and 19 controls.Results: Our results show that CSF α-Syn levels did not significantly differ across depressed and control participants, but α-Syn was directly associated with neurogranin levels, and indirectly linked to poorer memory ability.Conclusions: All in all, we found that α-Syn may be implicated in the association between late life MDD and synaptic dysfunction, although further research is needed to confirm these results.
Keyphrases
  • major depressive disorder
  • cerebrospinal fluid
  • bipolar disorder
  • mild cognitive impairment
  • cognitive decline
  • physical activity
  • working memory
  • risk assessment
  • sleep quality
  • subarachnoid hemorrhage