The research, reported in the journal Brain, found that a variant in the IL1RAP gene was associated with greater amyloid plaque accumulation over two years and had an even stronger effect than the well-known APOE e4 allele which is notorious for its association with the development of Alzheimer’s disease.
Using positron emission tomography imaging in nearly 500 individuals, the researchers assessed the levels of brain amyloid deposits at an initial visit and again two years later. A genome-wide analysis was then conducted to identify genetic variants associated with the rate of plaque accumulation during this two-year window. As predicted, APOE e4 was found to be associated with higher rates of plaque buildup. However, the investigators were surprised to find that IL1RAP, which codes for the key immune signaling factor Interleukin-1 Receptor Accessory Protein, showed an independent and even stronger influence on amyloid accumulation.
“This was an intriguing finding because IL1RAP is known to play a central role in the activity of microglia, the immune system cells that act as the brain’s “garbage disposal system” and the focus of heavy investigation in a variety of neurodegenerative diseases,” said Vijay K. Ramanan, M.D., Ph.D., postdoctoral researcher at the IU School of Medicine.
Alzheimer’s disease affects more than 5 million older Americans and there is currently no therapy proven to halt or reverse the underlying cause of the progressive symptoms of dementia. Researchers are increasingly focused on mechanisms involved with the deposit and clearance of amyloid plaques, particularly in early stages when symptoms are mild or not yet present. Scientists have long known from studies of brain tissue that microglia, the brain’s primary immune cell, gather around amyloid plaques. More recent evidence indicates that microglia play a role in clearing the deposits and PET scans show alterations in microglial activity in Alzheimer’s disease.
The new study in Brain found that the amyloid-associated IL1RAP variant was also associated with:
• A lower level of microglial activity as measured by PET scans.
• Greater atrophy of the temporal cortex, a region of the brain involved with memory.
• Faster cognitive decline.
• Greater likelihood among study participants of progression from mild cognitive impairment to Alzheimer’s disease.
“These findings suggest that targeting the IL1RAP immune pathway may be a viable approach for promoting the clearance of amyloid deposits and fighting an important cause of progression in Alzheimer’s disease,” said Andrew Saykin, Psy.D., director of the Indiana Alzheimer Disease Center and the national Alzheimer’s Disease Neuroimaging Initiative Genetics Core.
Dr. Saykin noted that there are available drugs that target the IL-1/IL1RAP pathway for rheumatologic and inflammatory conditions. There are also antibodies against IL1RAP that are being tested to treat certain types of leukemia. Those tools could be adapted for laboratory studies to evaluate their potential as Alzheimer’s disease therapies, he said.
The research was conducted using data from participants in the national Alzheimer’s Disease Neuroimaging Initiative, as well the Indiana Memory and Aging Study, the Religious Orders Study, and the Rush Memory and Aging Project, which are all longitudinal studies of older adults representing clinical stages along the continuum from normal aging to Alzheimer’s disease.
This research was supported by multiple grants from the National Institute on Aging, a component of the National Institutes of Health, as well as a consortium of private partners through the Foundation for the NIH.
In addition to Drs. Ramanan and Saykin, researchers contributing to this study were Shannon L. Risacher, Kwangsik Nho, Sungeun Kim, Li Shen, Brenna C. McDonald, Karmen K. Yoder, Gary D. Hutchins, John D.West, Eileen F. Tallman, Sujuan Gao, Tatiana M. Foroud, Martin R. Farlow of the IU School of Medicine; Philip L. De Jager and Robert C. Green, Harvard Medical School; David A. Bennett, Rush University Medical Centre; Paul S. Aisen and Arthur W. Toga, University of Southern California; Ronald C. Petersen and Clifford R. Jack Jr., Mayo Clinic Minnesota; William J. Jagust, University of California, Berkeley and Michael W. Weiner, University of California-San Francisco.
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