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Cerebrospinal Fluid Amyloid-β Oligomer Levels in Patients with Idiopathic Normal Pressure Hydrocephalus
BACKGROUND: The amyloid-β oligomers, consisting of 10–20 monomers (AβO(10–20)), have strong neurotoxicity and are associated with cognitive impairment in Alzheimer’s disease (AD). However, their role in patients with idiopathic normal pressure hydrocephalus (iNPH) is poorly understood. OBJECTIVE: We...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461658/ https://www.ncbi.nlm.nih.gov/pubmed/34275898 http://dx.doi.org/10.3233/JAD-210226 |
Sumario: | BACKGROUND: The amyloid-β oligomers, consisting of 10–20 monomers (AβO(10–20)), have strong neurotoxicity and are associated with cognitive impairment in Alzheimer’s disease (AD). However, their role in patients with idiopathic normal pressure hydrocephalus (iNPH) is poorly understood. OBJECTIVE: We hypothesized that cerebrospinal fluid (CSF) AβO(10–20) accumulates in patients with iNPH, and its clearance after CSF shunting contributes to neurological improvement. We measured CSF AβO(10–20) levels before and after CSF shunting in iNPH patients evaluating their diagnostic and prognostic role. METHODS: We evaluated two iNPH cohorts: “evaluation” (cohort-1) with 32 patients and “validation” (cohort-2) with 13 patients. Comparison cohorts included: 27 neurologically healthy controls (HCs), and 16 AD, 15 Parkinson’s disease (PD), and 14 progressive supranuclear palsy (PSP) patients. We assessed for all cohorts CSF AβO(10–20) levels and their comprehensive clinical data. iNPH cohort-1 pre-shunting data were compared with those of comparison cohorts, using cohort-2 for validation. Next, we compared cohort-1’s clinical and CSF data: 1) before and after CSF shunting, and 2) increased versus decreased AβO(10–20) levels at baseline, 1 and 3 years after shunting. RESULTS: Cohort-1 had higher CSF AβO(10–20) levels than the HCs, PD, and PSP cohorts. This result was validated with data from cohort-2. CSF AβO(10–20) levels differentiated cohort-1 from the PD and PSP groups, with an area under receiver operating characteristic curve of 0.94. AβO(10–20) levels in cohort-1 decreased after CSF shunting. Patients with AβO(10–20) decrease showed better cognitive outcome than those without. CONCLUSION: AβO(10–20) accumulates in patients with iNPH and is eliminated by CSF shunting. AβO(10–20) can be an applicable diagnostic and prognostic biomarker. |
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