Findings from a worldwide cohort of cognitively unimpaired individuals demonstrate that the presence of two canonical Alzheimer disease biomarkers — amyloid and tau — can reliably predict progression to mild cognitive impairment in the short-term. The results support the use of these biomarkers to diagnose preclinical Alzheimer disease in a clinical setting.
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Acknowledgements
This work was supported by National Institutes of Health grants R01AG059008 and R01AG073212, ADDF GC2013717 and the Barrow Neurological Foundation. We thank the staff of Neuroscience Publications at Barrow Neurological Institute for assistance with copy editing, manuscript preparation and submission.
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B.D. has consulted for Seq Biomarque and TransDermix. M.N.S. has ownership interests (stock or stock options) in Alzheon, Athira Pharma, Cortexyme/Quince Therapeutics, Lighthouse Pharmaceuticals, NeuroReserve, NeuroTau, Seq BioMarque, TransDermix, and uMethod Health; has consulted for Corium, Eisai, Lilly, NeuroTherapia, Novo Nordisk, Prothena, Roche-Genentech, Signant Health, Synaptogenix, and T3D; has received royalties from Humanix; and is on the board of directors of EIP Pharma.
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Sabbagh, M.N., DeCourt, B. Biomarker-based diagnosis of preclinical Alzheimer disease: time for the clinic?. Nat Rev Neurol 19, 71–72 (2023). https://doi.org/10.1038/s41582-022-00767-x
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DOI: https://doi.org/10.1038/s41582-022-00767-x