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Abstract Details

Associations of Renin-Angiotensin-System Inhibitor Use with Brain Insulin Signaling and Neuropathology
Aging, Dementia, and Behavioral Neurology
P3 - Poster Session 3 (5:30 PM-6:30 PM)
9-004

RAS inhibitor use has been associated with both improved peripheral insulin resistance and a reduced risk of dementia. However, whether RAS inhibitor use also improves brain insulin resistance and reduces neuropathology of dementia remains unclear.

To examine the association of renin-angiotensin system (RAS) inhibitor use with postmortem brain insulin signaling and dementia-related neuropathology.

Among Religious Orders Study participants,150 deceased and autopsied older individuals (75 with diabetes matched to 75 without by age at death, sex, and education) had measurements of insulin receptor substrate 1 (IRS-1) and RAC alpha serine/threonine protein kinase (AKT1) collected in the prefrontal cortex using ELISA and immunohistochemistry. Alzheimer’s disease (AD), brain infarcts, and cerebral vessel pathologies data were assessed by systematic neuropathologic evaluations. RAS inhibitor use was determined based on visual inspection of medication containers during study visits and coded using Medi-Span. Using regression analyses adjusted for age at death, sex, and diabetes, we examined the associations of RAS inhibitor use with brain insulin signaling measures and neuropathology.

RAS inhibitor users (N=90) included 54 with diabetes and 36 without. RAS inhibitor use was associated with lower pT308AKT1/total AKT1 (estimate=-0.397, p=0.019), a marker for brain insulin resistance, but not with pS307IRS-1/total IRS-1 or the density of pS616IRS-1 positive cells. RAS inhibitor use was not associated with the level of global AD pathology, nor with amyloid beta burden. However, RAS inhibitor use was associated with a lower neurofibrillary tangle density (estimate=-0.425, p=0.022). Furthermore, we found a significant interaction between diabetes and RAS inhibitors on tangle density (estimate=-1.174, p=0.001). Lastly, RAS inhibitor use was associated with more atherosclerosis (estimate=0.721, p=0.047), but not other cerebral blood vessel pathologies or cerebral infarcts.

These findings suggest that late-life RAS inhibitor use is associated with less insulin resistance and less accumulation of tau tangles in postmortem brain of older individuals. 

Authors/Disclosures
Han Tong, MBBS, PhD (Rush University Medical Center)
PRESENTER
Dr. Tong has nothing to disclose.
Ana Capuano No disclosure on file
Rupal Mehta (Rush University) No disclosure on file
David A. Bennett, MD (Rush University Medical Center) Dr. Bennett has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Origent. Dr. Bennett has received personal compensation in the range of $10,000-$49,999 for serving on a Scientific Advisory or Data Safety Monitoring board for AbbVie. Dr. Bennett has received personal compensation in the range of $5,000-$9,999 for serving as a Study section, DMC, NACA Council with NIH. Dr. Bennett has received personal compensation in the range of $10,000-$49,999 for serving as a invited lectures with AMCs. Dr. Bennett has received personal compensation in the range of $5,000-$9,999 for serving as a invited paper with National Academy of Sciences. Dr. Bennett has received personal compensation in the range of $5,000-$9,999 for serving as a lecture with National Academy of Neuropsychology.
Rexford Ahima (Johns Hopkins School of Medicine) No disclosure on file
Steven E. Arnold, MD (Massachusetts General Hospital) Dr. Arnold has received personal compensation in the range of $500-$4,999 for serving as a Consultant for EIP Pharma. Dr. Arnold has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eisai. Dr. Arnold has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sage Therapeutics. Dr. Arnold has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Cortexyme. Dr. Arnold has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Boyle Shaughnessy Law. Dr. Arnold has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Wolf Greenfield. Dr. Arnold has received personal compensation in the range of $500-$4,999 for serving as a Advisory Board Member with Bob's Last Marathon.
Zoe Arvanitakis, MD, MS, FAAN (Rush Alzheimer's Disease Center) Dr. Arvanitakis has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eisai Inc.. Dr. Arvanitakis has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Frontiers in Dementia. Dr. Arvanitakis has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for a private legal firm representing a governement entity. The institution of Dr. Arvanitakis has received research support from National Institutes of Health (NIH). The institution of Dr. Arvanitakis has received research support from Amylyx. The institution of Dr. Arvanitakis has received research support from Lilly. Dr. Arvanitakis has received personal compensation in the range of $500-$4,999 for serving as a Grant reviewer with The National Institutes of Health and California State (California Institute for Regenerative Medicine or CIRM). Dr. Arvanitakis has received personal compensation in the range of $500-$4,999 for serving as a Consultant and Educator with Summus Global, Inc.