The effects of normal aging on amyloid‐β deposition in nondemented adults with Down syndrome as imaged by carbon 11–labeled Pittsburgh compound B. Issue 4 (13th June 2015)

• Record Type: Journal Article
• Authors: Lao, Patrick J.; Betthauser, Tobey J.; Hillmer, Ansel T.; Price, Julie C.; Klunk, William E.; Mihaila, Iulia; Higgins, Andrew T.; Bulova, Peter D.; Hartley, Sigan L.; Hardison, Regina; Tumuluru, Rameshwari V.; Murali, Dhanabalan; Mathis, Chester A.; Cohen, Annie D.; Barnhart, Todd E.; Devenny, Darlynne A.; Mailick, Marsha R.; Johnson, Sterling C.; Handen, Benjamin L.; Christian, Bradley T.
• Is Part Of: Alzheimer's & dementia. Volume 12:Issue 4(2016)
• Page Start: 380
• Page End: 390
• Publication Date: 2015-06-13
• Subjects: Down syndrome -- Alzheimer's disease -- Amyloid imaging -- PiB -- Aging; Alzheimer's disease -- Periodicals; Alzheimer Disease -- Periodicals; Dementia -- Periodicals; Démence; Maladie d'Alzheimer; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.83
• DOI: 10.1016/j.jalz.2015.05.013
• Languages: English
• ISSNs: 1552-5260

Abstract

Abstract: Introduction: In Down syndrome (DS), the overproduction of amyloid precursor protein is hypothesized to predispose young adults to early expression of Alzheimer‐like neuropathology. Methods: PET imaging with carbon 11–labeled Pittsburgh compound B examined the pattern of amyloid‐β deposition in 68 nondemented adults with DS (30–53 years) to determine the relationship between deposition and normal aging. Standard uptake value ratio (SUVR) images were created with cerebellar gray matter as the reference region. Results: Multiple linear regression revealed slight but highly significant (corrected P < .05) positive correlations between SUVR and age. The striatum showed the strongest correlation, followed by precuneus, parietal cortex, anterior cingulate, frontal cortex, and temporal cortex. Conclusion: There is an age‐related amyloid‐β deposition in the DS population, but as a pattern of elevated cortical retention becomes apparent, the correlation of SUVR with age ceases to be significant. Factors unrelated to aging may drive an increase in deposition during early Alzheimer's disease pathogenesis.