The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×

OBJECTIVE: Differentiation of geriatric major depression from Alzheimer’s disease is hampered by overlapping symptoms. Increased CSF concentrations of tau protein phosphorylated at threonine 231 (p-tau231) have been suggested as a biomarker for Alzheimer’s disease. The authors asked whether p-tau231 levels improve the differential diagnosis between geriatric major depression and Alzheimer’s disease. METHOD: Included were 34 depression subjects, 64 with probable Alzheimer’s disease, 17 with possible Alzheimer’s disease, and 21 healthy comparison subjects. P-tau231 concentrations were measured with an enzyme-linked immunosorbent assay. RESULTS: P-tau231 levels were significantly higher in Alzheimer’s disease than in geriatric major depression patients and healthy comparison subjects. For differentiation of probable Alzheimer’s disease from major depression, p-tau231 correctly allocated 87% of subjects. When possible mild Alzheimer’s disease was compared to major depression, p-tau231 correctly allocated 78% of subjects. CONCLUSIONS: CSF p-tau231 should be evaluated as a potential biological marker for differentiation of geriatric depression from Alzheimer’s disease.