The aging brain suffers from progressive brain tissue loss, putting hundreds of millions of us at risk for memory loss and dementia with no known cure. We recently discovered, in studies related to physical activity, growth factors, and homocysteine, several new leads about what may promote brain integrity. These variables interact with each other, with inflammation, and with brain structure and disease risk in complex and striking ways. To resist the looming epidemic of degenerative disease, we must determine how such variables deter brain decline. We will map, with unprecedented sensitivity, how these vital processes, which are targetable with interventions, relate to brain structure. We also combine brain measures to predict, with machine learning who will imminently decline. We relate brain and cognitive decline in 3 populations to (1) an inflammatory marker and related neurodegenerative risk genes, (2) growth factor and homocysteine levels, and (3) physical exercise. We will discover how these variables interact to promote or deter brain disease, in our regions of interest (ROIs) - the hippocampus, prefrontal cortex (PFC), and cingulate gyrus. This work is crucial to combat diseases such as Alzheimer's disease (AD) and schizophrenia (SZ), among others that are both related to these variables and marked by deficits in these ROIs. We will also survey the whole brain with novel brain mapping methods. Physical activity promotes human brain regeneration in these regions, in part through its effects on growth factors. It decreases inflammation and homocysteine levels, both of which relate to hippocampal integrity. Our project will boost power in clinical trials by identifying targetable disease-driving mechanisms. Building on our recent discoveries, we use (1) genotyped variants in inflammation-related genes, (2) a controllable "environmental" variable (exercise), and (3) peripheral measures related to inflammation, neurogenesis, and homocysteine to assess integrity of the hippocampus, PFC, and cingulate gyrus, and their progressive decline. We examine three populations already scanned with MRI: the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort (566 AD, MCI, and normal elderly subjects), the Cardiovascular Health Study (CHS;517 AD, MCI, and control subjects;of whom 85 have our targeted serum measures), and the Dominantly Inherited Alzheimer Network, composed of younger adults from families with autosomal dominant AD mutations (DIAN;~400: ~20% with AD;~50% mutation carriers). We will assess: 3/4 how candidate gene variants associated with AD and inflammation (see Approach) relate to a serum marker of inflammation (tumor necrosis factor alpha;TNF?), and to hippocampal volume. 3/4 how serum levels of growth factors and homocysteine relate to hippocampal, PFC, and cingulate volume. 3/4 how exercise levels affect hippocampal volume;how growth factors and TNF? modulate this relationship. 3/4 how baseline serum levels of growth factors, TNF?, and homocysteine, polymorphisms in related genes, and exercise together predict brain and cognitive changes over a 2-year follow-up period.

Public Health Relevance

Our project will have major impact on public health by discovering how three key processes (inflammation, brain growth factors, and exercise) relate to brain structure and brain decline over a 2-year period. Physical exercise boosts the ability of growth factors to promote regeneration in the hippocampus, which is important in memory;inflammation (which has many causes, including disease) decreases that ability. Our last 20 years of work revealed how Alzheimer's disease, schizophrenia, depression, and drug abuse involve hippocampal deficits and brain atrophy. Here we will evaluate in three large populations how growth factors, inflammation, and exercise work together to protect or harm the human brain - identifying promising directions for treatment, prevention, and a mechanistic understanding of diseases and disorders such as Alzheimer's disease, schizophrenia, and drug addiction.

Agency
National Institute of Health (NIH)
Type
Multi-Year Funded Research Project Grant (RF1)
Project #
1RF1AG041915-01A1
Application #
8696676
Study Section
Molecular Neurogenetics Study Section (MNG)
Program Officer
Wise, Bradley C
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Southern California
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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