James E. Galvin, United States of America

University of Miami Miller School of Medicine Neurology
James E. Galvin, M.D., M.P.H. is Professor of Neurology at the University of Miami Miller School of Medicine. He is Founding Director of the Comprehensive Program for Brain Health and Chief, Cognitive Neurology for Palm Beach and Broward County leading brain health and neurodegenerative disease clinical and research programs. Dr. Galvin has authored over 260 scientific publications, 25 book chapters, and 3 textbooks on healthy brain aging, cognitive health, memory loss, Alzheimer’s disease, Lewy Body dementia, and related disorders. Dr. Galvin’s research has been funded by the National Institutes of Health, Centers for Disease Control, Florida Department of Health, and numerous Private and Family Foundations.

Author Of 2 Presentations

DESIGNING DEMENTIA PREVENTION STUDIES: USING PROXY BIOMARKERS TO IDENTIFY AT-RISK INDIVIDUALS

Session Type
SYMPOSIUM
Date
10.03.2021, Wednesday
Session Time
10:00 - 12:00
Room
On Demand Symposia A
Lecture Time
11:15 - 11:30
Session Icon
On-Demand

Abstract

Abstract Body

Aims: The prevention of Alzheimer Disease and Related Dementias (ADRD) may be possible through multimodal interventions that combine lifestyle modification, risk reduction, health promotion, and co-morbidity management using precision medicine approaches. A driving factor in ADRD research is the search for markers of amyloid and tau deposition, however up to 40% of ADRD attributable risk may be explained by other factors and pathologies. We have reported novel non-cognitive prodromal predictors of dementia including gait and mobility impairment, sarcopenia, slowed psychomotor performance, declining physical functionality, and depression.

Methods: In a study of 400 older adults (age 75.3+9.2y; 46.9% female, 50.1% positive family history, 64.6% subjective complaints, 38.1% ApoE 4 carriers) using a comprehensive deep-phenotype evaluation to explore non-MRI/PET/CSF biomarkers to test proxy biomarkers of at-risk individuals compared with healthy controls. These proxy markers include computerized gait analyses, optical coherence tomography, dietary patterns, and serum measures of pathology

Results: Individuals at-risk for ADRD and those with mild cognitive impairment show declining gait velocity on dual cognitive-motor tasks, thinning of the retinal nerve cell layers, poorer MIND diet scores, lower “dosages” of physical and cognitive activity participation, and higher vascular risk scores measured with a modified CAIDE score compared with healthy controls. Finally, plasma ADRD biomarkers may discriminate healthy controls from individuals with pre-clinical ADRD.

Conclusions: Efforts to prevent cognitive decline may be enhanced by examining proxy biomarkers of neurodegenerative disease that are less expensive, less invasive and more accessible. Incorporating these findings into multimodal interventions may offer novel approaches to preventing ADRD.

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Presenter of 4 Presentations

DESIGNING DEMENTIA PREVENTION STUDIES: USING PROXY BIOMARKERS TO IDENTIFY AT-RISK INDIVIDUALS

Session Type
SYMPOSIUM
Date
10.03.2021, Wednesday
Session Time
10:00 - 12:00
Room
On Demand Symposia A
Lecture Time
11:15 - 11:30
Session Icon
On-Demand

Abstract

Abstract Body

Aims: The prevention of Alzheimer Disease and Related Dementias (ADRD) may be possible through multimodal interventions that combine lifestyle modification, risk reduction, health promotion, and co-morbidity management using precision medicine approaches. A driving factor in ADRD research is the search for markers of amyloid and tau deposition, however up to 40% of ADRD attributable risk may be explained by other factors and pathologies. We have reported novel non-cognitive prodromal predictors of dementia including gait and mobility impairment, sarcopenia, slowed psychomotor performance, declining physical functionality, and depression.

Methods: In a study of 400 older adults (age 75.3+9.2y; 46.9% female, 50.1% positive family history, 64.6% subjective complaints, 38.1% ApoE 4 carriers) using a comprehensive deep-phenotype evaluation to explore non-MRI/PET/CSF biomarkers to test proxy biomarkers of at-risk individuals compared with healthy controls. These proxy markers include computerized gait analyses, optical coherence tomography, dietary patterns, and serum measures of pathology

Results: Individuals at-risk for ADRD and those with mild cognitive impairment show declining gait velocity on dual cognitive-motor tasks, thinning of the retinal nerve cell layers, poorer MIND diet scores, lower “dosages” of physical and cognitive activity participation, and higher vascular risk scores measured with a modified CAIDE score compared with healthy controls. Finally, plasma ADRD biomarkers may discriminate healthy controls from individuals with pre-clinical ADRD.

Conclusions: Efforts to prevent cognitive decline may be enhanced by examining proxy biomarkers of neurodegenerative disease that are less expensive, less invasive and more accessible. Incorporating these findings into multimodal interventions may offer novel approaches to preventing ADRD.

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Moderator of 1 Session

LIVE SYMPOSIUM DISCUSSION

LIVE DISCUSSION - DIGITAL-END POINTS AND ARTIFICIAL INTELLIGENCE

Date
14.03.2021, Sunday
Session Time
17:30 - 18:00
Session Icon
Live