CSF neurogranin or tau distinguish typical and atypical Alzheimer disease. Issue 2 (11th January 2018)

• Record Type: Journal Article
• Authors: Wellington, Henrietta; Paterson, Ross W.; Suárez‐González, Aida; Poole, Teresa; Frost, Chris; Sjöbom, Ulrika; Slattery, Catherine F.; Magdalinou, Nadia K.; Lehmann, Manja; Portelius, Eric; Fox, Nick C.; Blennow, Kaj; Zetterberg, Henrik; Schott, Jonathan M.
• Is Part Of: Annals of clinical and translational neurology. Volume 5:Issue 2(2018)
• Page Start: 162
• Page End: 171
• Publication Date: 2018-01-11
• Subjects: Nervous system -- Diseases -- Periodicals; Neurology -- Periodicals; 616.8005
• DOI: 10.1002/acn3.518
• Languages: English
• ISSNs: 2328-9503

Abstract

Abstract: Objective: To assess whether high levels of cerebrospinal fluid neurogranin are found in atypical as well as typical Alzheimer's disease. Methods: Immunoassays were used to measure cerebrospinal fluid neurogranin in 114 participants including healthy controls ( n = 27), biomarker‐proven amnestic Alzheimer's disease ( n = 68), and the atypical visual variant of Alzheimer's ( n = 19) according to international criteria. CSF total‐tau, Aβ42, and neurofilament light concentrations were investigated using commercially available assays. All affected individuals had T1‐weighted volumetric MR images available for analysis of whole and regional brain volumes. Associations between neurogranin, brain volumes, total‐tau, Aβ42, and neurofilament light were assessed. Results: Median cerebrospinal fluid neurogranin concentrations were higher in typical and atypical Alzheimer's compared to controls ( P < 0.001 and P = 0.005). Both neurogranin and total‐tau concentrations, but not neurofilament light and Aβ42, were higher in typical Alzheimer's compared to atypical patients ( P = 0.004 and P = 0.03). There were significant differences in the left hippocampus and right and left superior parietal lobules in atypical patients, which were larger ( P = 0.03) and smaller ( P = 0.001 and P < 0.001), respectively, compared to typical patients. We found no evidence of associations between neurogranin and brain volumes but a strong association with total‐tau ( P < 0.001) and a weaker association with neurofilament light ( P = 0.005). Interpretation: These results show significant differences in neurogranin and total‐tau between typical and atypical patients, which may relate to factors other than disease topography. The differential relationships between neurogranin, total‐tau and neurofilament light in the Alzheimer's variants, provide evidence for mechanistically distinct and coupled markers of neurodegeneration.