Sequence of Alzheimer disease biomarker changes in cognitively normal adults
Jingqin Luo, Folasade Agboola, Elizabeth Grant, Colin L. Masters, Marilyn Albert, Sterling C. Johnson, Eric McDade, Jonathan Vöglein, Anne M. Fagan, Tammie L.S. Benzinger, Parinaz Massoumzadeh, Jason Hassenstab, Randall J. Bateman, John C. Morris, Richard J. Perrin, Jasmeer P. Chhatwal, Mathias Jucker, Bernardino Ghetti, Carlos Cruchaga, Neill R. Graff‐Radford, Peter R. Schofield, Hiroshi Mori, Chengjie Xiong
Abstract
OBJECTIVE: To determine the ordering of changes in Alzheimer disease (AD) biomarkers among cognitively normal individuals. METHODS: C] benzothiazole tracer Pittsburgh compound B (PiB), MRI-based brain structures, and clinical/cognitive outcomes harmonized from 8 studies, collectively involving 3,284 cognitively normal individuals 18 to 101 years of age, were analyzed. The age at which each marker exhibited an accelerated change (called the change point) was estimated and compared across the markers. RESULTS: ratio, albeit not significantly different from that for PiB SUVR, occurred significantly earlier than that for CSF Tau, Ptau, MRI markers, and the cognitive composite. Adjusted analyses confirmed that accelerated changes in CSF Tau, Ptau, MRI markers, and the cognitive composite occurred at ages not significantly different from each other. CONCLUSIONS: Our findings support the hypothesized early changes of amyloid in preclinical AD and suggest that changes in neuronal injury and neurodegeneration markers occur close in time to cognitive decline.