This is an application for a one-time renewal of K24 Midcareer Investigator Award in aging and Alzheimer's disease (AD) patient-oriented research. The candidate, Reisa A. Sperling, M.D. M.MSc., is a neurologist with a strong track record as a productive clinical investigator and research mentor. The overarching aims of the candidates' research program are to: 1) elucidate the neural underpinnings of memory decline in aging and early AD; 2) develop sensitive imaging markers to track the progression of early AD; and 3) facilitate earlier intervention with potential disease-modifying treatments in the preclinical stags of AD. The candidate currently leads several ongoing NIH and foundation-funded multimodality imaging projects in aging, preclinical, and prodromal AD, as well as a large secondary prevention trial in preclinical AD. The candidate will continue to use her funded research as a platform for the mentorship of young patient-oriented investigators, and to promote a multidisciplinary approach to the study of cognitive aging and early AD. The candidates' mentees have the opportunity to train in functional, structural, and molecular imaging techniques, cognitive neuroscience, neuropsychological assessment, biostatistics, and clinical trial design as they apply to aging and early AD research, drawing on expertise from an outstanding group of collaborators. Trainees will also be able to participate in research seminars, statistical courses and imaging workshops, career development and grant- writing workshops provided by Harvard Catalyst CTSC, T32 and other training grants, as well as formal didactic course work through the Catalyst, Harvard Medical School, Harvard School of Public Health, and Massachusetts Institute of Technology. A new component proposed for the K24 renewal is mentoring on mentoring to teach developing investigators how to effectively mentor their own mentees as they transition to independence. The candidate has successfully mentored more than 20 fellow and junior faculty trainees over the past 5 years of the initial K24 award, including multiple women and several minority young researchers, who have published over 60 manuscripts and have garnered multiple honors and funding for their work. The K24 renewal research project proposes to investigate the influence of sex (gender) on AD imaging biomarkers and risk of cognitive decline, which will provide many new research opportunities for the candidate's mentees. To further her own continued professional development through the K24 mechanism, the candidate will acquire training in sex-based biology and advanced analytic methodology, and will continue to enhance her mentoring skills through formal mentoring and leadership training. This K24 renewal is critically important for the candidate to continue to grow and foster her clinical research career development and, most essentially, to protect her time to mentor the next generation of investigators committed to early AD patient-oriented research.

Public Health Relevance

The candidate's research program seeks to understand the cause of memory decline in older individuals, to utilize imaging tools to detect the earliest signs of Alzheimer's disease (AD), and to find effective treatments to prevent memory loss due to AD. The candidate will use the K24 award renewal to expand her mentoring program to train new investigators for clinical research careers in patient-oriented AD research.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Midcareer Investigator Award in Patient-Oriented Research (K24)
Project #
2K24AG035007-06
Application #
9032789
Study Section
Neuroscience of Aging Review Committee (NIA)
Program Officer
Hsiao, John
Project Start
2009-12-01
Project End
2021-03-31
Budget Start
2016-04-15
Budget End
2017-03-31
Support Year
6
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
Hanseeuw, Bernard J; Jonas, Victoria; Jackson, Jonathan et al. (2018) Association of anxiety with subcortical amyloidosis in cognitively normal older adults. Mol Psychiatry :
Jacobs, Heidi I L; Hedden, Trey; Schultz, Aaron P et al. (2018) Structural tract alterations predict downstream tau accumulation in amyloid-positive older individuals. Nat Neurosci 21:424-431
d'Oleire Uquillas, Federico; Jacobs, Heidi I L; Hanseeuw, Bernard et al. (2018) Interactive versus additive relationships between regional cortical thinning and amyloid burden in predicting clinical decline in mild AD and MCI individuals. Neuroimage Clin 17:388-396
Buckley, Rachel F; Mormino, Elizabeth C; Amariglio, Rebecca E et al. (2018) Sex, amyloid, and APOE ?4 and risk of cognitive decline in preclinical Alzheimer's disease: Findings from three well-characterized cohorts. Alzheimers Dement 14:1193-1203
Rieckmann, Anna; Johnson, Keith A; Sperling, Reisa A et al. (2018) Dedifferentiation of caudate functional connectivity and striatal dopamine transporter density predict memory change in normal aging. Proc Natl Acad Sci U S A 115:10160-10165
d'Oleire Uquillas, Federico; Jacobs, Heidi I L; Biddle, Kelsey D et al. (2018) Regional tau pathology and loneliness in cognitively normal older adults. Transl Psychiatry 8:282
Donovan, Nancy J; Locascio, Joseph J; Marshall, Gad A et al. (2018) Longitudinal Association of Amyloid Beta and Anxious-Depressive Symptoms in Cognitively Normal Older Adults. Am J Psychiatry 175:530-537
Vannini, Patrizia; Amariglio, Rebecca; Hanseeuw, Bernard et al. (2017) Memory self-awareness in the preclinical and prodromal stages of Alzheimer's disease. Neuropsychologia 99:343-349
Pr?kovska, Vesna; Huijbers, Willem; Schultz, Aaron et al. (2017) Epicenters of dynamic connectivity in the adaptation of the ventral visual system. Hum Brain Mapp 38:1965-1976
Dumurgier, Julien; Hanseeuw, Bernard J; Hatling, Frances B et al. (2017) Alzheimer's Disease Biomarkers and Future Decline in Cognitive Normal Older Adults. J Alzheimers Dis 60:1451-1459

Showing the most recent 10 out of 131 publications