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High-probability grants
According to our matching algorithm, Rahul Desikan is the likely recipient of the following grants.
| Years |
Recipients |
Code |
Title / Keywords |
Matching
score |
| 2019 |
Desikan, Rahul S |
R03Activity Code Description:
To provide research support specifically limited in time and amount for studies in categorical program areas. Small grants provide flexibility for initiating studies which are generally for preliminary short-term projects and are non-renewable. |
Sex in Alzheimer Disease @ University of California, San Francisco
PROJECT SUMMARY With the aging of the US population and high costs associated with caring for the cognitively impaired elderly, identifying older individuals at greatest risk for developing Alzheimer's disease (AD) is of utmost societal and clinical importance. Currently no treatments effectively slow the progression of AD or other causes of cognitive decline, but billions of dollars are being invested to develop effective treatments. Development of inexpensive, genomic methods that go beyond APOE to identify individuals at risk for cognitive decline has the potential to greatly accelerate the development of new treatments. The overall significance of this project is that it will use a validated polygenic score to more comprehensively understand when older men and women are at highest risk for cognitive decline and Alzheimer's neurodegeneration. Using an age-dependent approach, we have recently developed and validated a novel `polygenic hazard score' (PHS) for quantifying AD dementia age of onset, even among APOE E3/3 individuals, who constitute the majority of all US individuals with AD dementia. In this proposal, our objective is to comprehensively assess whether sex differences influence how PHS predicts cognitive decline and AD neurodegeneration and how age influences this relationship. Leveraging genotypic and multi-modal phenotypic data from several existing NIH-funded cohorts (total n > 7,000), we will investigate whether age-dependent sex differences modify cognitive decline, postmortem and in vivo AD neuropathology and medial temporal lobe volume loss.
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0.919 |