4.5 Article

Depressive Symptoms and Tau Accumulation in the Inferior Temporal Lobe and Entorhinal Cortex in Cognitively Normal Older Adults: A Pilot Study

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 59, Issue 3, Pages 975-985

Publisher

IOS PRESS
DOI: 10.3233/JAD-170001

Keywords

Alzheimer's disease; amyloid; cognitively normal; depression; depressive symptoms; positron emission tomography; tau

Categories

Funding

  1. Muriel Silberstein Alzheimer's Disease Research Fund
  2. MADRC [P01 AG036694, R01 AG037497, R01 AG046396, P50 AG005134, K24 AG035007]
  3. Harvard NeuroDiscovery Center
  4. Eli Lilly and Company

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Background: Depressive symptoms are common in older adults and associated with increased morbidity and cognitive decline. These symptoms occur during preclinical and prodromal stages of Alzheimer's disease (AD), but their relationship to tau, one of the main AD proteinopathies, is poorly understood. Objective: The objective of this study was to investigate the cross-sectional association between depressive symptoms and cerebral tau [F-18 T807 (also known as F-18-AV-1451) tau positron emission tomography (PET) imaging] in cognitively normal (CN) older adults. Methods: We measured depressive symptoms using the Geriatric Depression Scale (GDS), and in vivo cerebral tau using T807 PET in 111 CN older adults. We employed general linear regression models to evaluate the relationship of GDS score regressed on entorhinal cortex (EC) or inferior temporal (IT) tau in separate backward elimination models. Other predictors included age, sex, and in secondary analyses, amyloid (Pittsburgh Compound B PET). Results: Higher GDS was significantly associated with greater IT tau (partial r = 0.188, p = 0.050) and marginally associated with greater EC tau (partial r = 0.183, p = 0.055). In additional analyses including both linear and quadratic age terms, we found a significant U-shaped relation of GDS to age (p = 0.001). Conclusions: Results suggest that IT and EC tau are modestly associated with depressive symptoms in CN older adults. Findings suggest a link between depressive symptoms and tau-mediated neurodegeneration in a region vulnerable in AD. Future longitudinal studies examining the association of more severe depressive symptoms and cerebral tau accumulation are needed to substantiate this finding and to guide prevention and treatment in AD.

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