Citations 471

P3‐152: Levels of TAU Protein in Plasma are Associated with Neurodegeneration and Cognitive Function in a Population‐Based Elderly Cohort

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_18 | Pages: No page available

10.1016/j.jalz.2016.06.1812

P3‐146: Regional Beta‐Amyloid Pet Comparison Across Atypical and Typical Variants of Alzheimer’s Disease

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_18 | Pages: No page available

10.1016/j.jalz.2016.06.1806

IC‐P‐006: Regional Beta‐Amyloid Pet Comparison Across Atypical and Typical Variants of Alzheimer’s Disease

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_1 | Pages: No page available

10.1016/j.jalz.2016.06.016

IC‐P‐201: Predicting Amyloid Deposition in Progressive Aphasia and Apraxia of Speech Using Clinical and Mri Data

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_3 | Pages: No page available

10.1016/j.jalz.2016.06.233

Varying Degrees of Temporoparietal Hypometabolism on FDG-PET Reveal Amyloid-Positive Logopenic Primary Progressive Aphasia is not a Homogeneous Clinical Entity

Journal of Alzheimer's Disease | October 14, 2016 | Volume: 55 | Issue: 3 | Pages: 1019-1029

10.3233/jad-160614 | PMID 27802232

Practice effects and longitudinal cognitive change in clinically normal older adults differ by Alzheimer imaging biomarker status

The Clinical Neuropsychologist | October 11, 2016 | Volume: 31 | Issue: 1 | Pages: 99-117

10.1080/13854046.2016.1241303 | PMID 27724156

Defining imaging biomarker cut points for brain aging and Alzheimer's disease

Alzheimer's & Dementia | October 5, 2016 | Volume: 13 | Issue: 3 | Pages: 205-216

10.1016/j.jalz.2016.08.005 | PMID 27697430

Abstract Introduction Our goal was to develop cut points for amyloid positron emission tomography (PET), tau PET, flouro‐deoxyglucose (FDG) PET, and MRI cortical thickness. Methods We examined five methods for determining cut points. Results The reliable worsening method produced a cut point only for amyloid PET. The specificity, sensitivity, and accuracy of cognitively impaired versus young clinically normal (CN) methods labeled the most people abnormal and all gave similar cut points for tau PET, FDG PET, and cortical thickness. Cut points defined using the accuracy of cognitively impaired versus age‐matched CN method labeled fewer people abnormal. Discussion In the future, we will use a single cut point for amyloid PET (standardized uptake value ratio, 1.42; centiloid, 19) based on the reliable worsening cut point method. We will base lenient cut points for tau PET, FDG PET, and cortical thickness on the accuracy of cognitively impaired versus young CN method and base conservative cut points on the accuracy of cognitively impaired versus age‐matched CN method.
Comparison of Gait Parameters for Predicting Cognitive Decline: The Mayo Clinic Study of Aging

Journal of Alzheimer’s Disease | September 23, 2016 | Volume: 55 | Issue: 2 | Pages: 559-567

10.3233/jad-160697 | PMID 27662317

Background: Previous studies reported that slower gait speed might predict cognitive impairment and dementing illnesses, supporting the role of gait speed as a possible subclinical marker of cognitive impairment. However, the predictive value of other gait parameters for cognitive decline is unclear. Objective: To investigate and compare the association with, and prediction of, specific gait parameters for cognition in a population-based sample. Methods: The analysis included 3,426 cognitively normal participants enrolled in the Mayo Clinic Study of Aging. At baseline and every 15 months (mean follow-up = 1.93 years), participants had a study coordinator evaluation, neurological examination, and a neuropsychological assessment using nine tests that covered four domains. Gait parameters were assessed with the GAITRite ® instrument. General linear mixed effects models were used to compute the annualized rate of change in cognitive domain z-scores, controlling for age, sex, education, depression, comorbidities, body mass index, APOE ɛ 4 allele, and visit number, and excluding individuals with a history of stroke, alcoholism, Parkinson’s disease, subdural hematoma, and normal pressure hydrocephalus. Results: Spatial (stride length), temporal (ambulatory time, gait speed, step count, cadence, double support time), and spatiotemporal (cadence) gait parameters, and greater intraindividual variability in stride length, swing time, and stance time were associated with a significant decline in global cognition and in specific domains including memory, executive function, visuospatial, and language. Conclusions: Spatial, temporal, and spatiotemporal measures of gait and greater variability of gait parameters were associated with and predictive of both global- and domain-specific cognitive decline.
Mediterranean diet, micronutrients and macronutrients, and MRI measures of cortical thickness

Alzheimer's & Dementia | July 26, 2016 | Volume: 13 | Issue: 2 | Pages: 168-177

10.1016/j.jalz.2016.06.2359 | PMID 27461490

AbstractIntroductionThe Mediterranean diet (MeDi) is associated with reduced risk of cognitive impairment, but it is unclear whether it is associated with better brain imaging biomarkers.MethodsAmong 672 cognitively normal participants (mean age, 79.8 years, 52.5% men), we investigated associations of MeDi score and MeDi components with magnetic resonance imaging measures of cortical thickness for the four lobes separately and averaged (average lobar).ResultsHigher MeDi score was associated with larger frontal, parietal, occipital, and average lobar cortical thickness. Higher legume and fish intakes were associated with larger cortical thickness: legumes with larger superior parietal, inferior parietal, precuneus, parietal, occipital, lingual, and fish with larger precuneus, superior parietal, posterior cingulate, parietal, and inferior parietal. Higher carbohydrate and sugar intakes were associated with lower entorhinal cortical thickness.DiscussionIn this sample of elderly persons, higher adherence to MeDi was associated with larger cortical thickness. These cross‐sectional findings require validation in prospective studies.
Levels of tau protein in plasma are associated with neurodegeneration and cognitive function in a population‐based elderly cohort

Alzheimer's & Dementia | July 18, 2016 | Volume: 12 | Issue: 12 | Pages: 1226-1234

10.1016/j.jalz.2016.06.001 | PMID 27436677

Abstract Introduction Tau protein levels in plasma may be a marker of neuronal damage. We examined associations between plasma tau levels and Alzheimer's disease (AD)–related magnetic resonance imaging (MRI) and positron emission tomography (PET) neuroimaging measures among nondemented individuals. Methods Participants included 378 cognitively normal (CN) and 161 mild cognitive impairment (MCI) individuals enrolled in the Mayo Clinic Study of Aging with concurrent neuropsychological measures and amyloid PET, fluorodeoxyglucose PET, and MRI. Baseline plasma tau levels were measured using the Quanterix Simoa‐HD1 tau assay. Results Plasma tau levels were higher in MCI compared with CN (4.34 vs. 4.14 pg/mL, P = .078). In regression models adjusted for age, gender, education, and APOE , higher plasma tau was associated with worse memory performance (b = −0.30, P = .02) and abnormal cortical thickness in an AD signature region (odds ratio = 1.80, P = .018). Discussion Plasma tau is associated with cortical thickness and memory performance. Longitudinal studies will better elucidate the associations between plasma tau, neurodegeneration, and cognition.