期刊论文详细信息
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring | |
Proteomic profiles of prevalent mild cognitive impairment and Alzheimer's disease among adults with Down syndrome | |
Deborah Pang1  Sharon J. Krinsky‐McHale1  Melissa Petersen2  James Hall3  Sid E. O'Bryant3  Joseph H. Lee4  Nicole Schupf4  Wayne Silverman5  Fan Zhang6  | |
[1]Department of Psychology NYS Institute for Basic Research in Developmental Disabilities Staten Island New York USA | |
[2]Institute for Translational Research Department of Family Medicine University of North Texas Health Science Center Fort Worth Texas USA | |
[3]Institute for Translational Research Department of Pharmacology and Neuroscience University of North Texas Health Science Center Fort Worth Texas USA | |
[4]Taub Institute for Research on Alzheimer's Disease and the Aging Brain Columbia University New York New York | |
[5]University of California Irvine California USA | |
[6]Vermont Genetics Network University of Vermont Burlington Vermont USA | |
关键词: blood based; biomarkers; plasma; Down syndrome; Alzheimer's disease; | |
DOI : 10.1002/dad2.12023 | |
来源: DOAJ |
【 摘 要 】
Abstract Introduction We sought to determine if a proteomic profile approach developed to detect Alzheimer's disease (AD) in the general population would apply to adults with Down syndrome (DS). Methods Plasma samples were obtained from 398 members of a community‐based cohort of adults with DS. A total of n = 186 participants were determined to be non‐demented and without mild cognitive impairment (MCI) at baseline and throughout follow‐up; n = 50 had prevalent MCI; n = 42 had prevalent AD. Results The proteomic profile yielded an area under the curve (AUC) of 0.92, sensitivity (SN) = 0.80, and specificity (SP) = 0.98 detecting prevalent MCI. For detecting prevalent AD, the proteomic profile yielded an AUC of 0.89, SN = 0.81, and SP = 0.97. The overall profile closely resembled our previously published profile of AD in the general population. Discussion These data provide evidence of the applicability of our blood‐based algorithm for detecting MCI/AD among adults with DS.【 授权许可】
Unknown