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Proteomic profiles for Alzheimer's disease and mild cognitive impairment among adults with Down syndrome spanning serum and plasma: An Alzheimer's Biomarker Consortium-Down Syndrome (ABC-DS) study.
Petersen, Melissa E; Zhang, Fan; Schupf, Nicole; Krinsky-McHale, Sharon J; Hall, James; Mapstone, Mark; Cheema, Amrita; Silverman, Wayne; Lott, Ira; Rafii, Michael S; Handen, Benjamin; Klunk, William; Head, Elizabeth; Christian, Brad; Foroud, Tatiana; Lai, Florence; Rosas, H Diana; Zaman, Shahid; Ances, Beau M; Wang, Mei-Cheng; Tycko, Benjamin; Lee, Joseph H; O'Bryant, Sid.
Affiliation
  • Petersen ME; Department of Family Medicine Institute for Translational Research University of North Texas Health Science Center Fort Worth Texas USA.
  • Zhang F; Vermont Genetics Network University of Vermont Burlington Vermont USA.
  • Schupf N; Taub Institute for Research on Alzheimer's Disease and the Aging Brain Columbia University Irving Medical Center New York New York USA.
  • Krinsky-McHale SJ; G.H. Sergievsky Center Columbia University Irving Medical Center New York New York USA.
  • Hall J; Department of Epidemiology, Mailman School of Public Health Columbia University New York New York USA.
  • Mapstone M; Department of Neurology Neurological Institute Columbia University Irving Medical Center New York New York USA.
  • Cheema A; Department of Psychiatry Columbia University Medical Center New York New York USA.
  • Silverman W; Department of Psychology NYS Institute for Basic Research in Developmental Disabilities Staten Island New York USA.
  • Lott I; Department of Pharmacology and Neuroscience Institute for Translational Research University of North Texas Health Science Center Fort Worth Texas USA.
  • Rafii MS; Department of Neurology University of California Irvine California USA.
  • Handen B; Georgetown University Medical Center Washington District of Columbia USA.
  • Klunk W; Department of Pediatrics, School of Medicine University of California Irvine California USA.
  • Head E; Department of Pediatrics, School of Medicine University of California Irvine California USA.
  • Christian B; Department of Neurology, Keck School of Medicine University of Southern California San Diego California USA.
  • Foroud T; Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Lai F; Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Rosas HD; Department of Pathology University of California Irvine California USA.
  • Zaman S; Department of Medical Physics and Psychiatry University of Wisconsin Madison Madison Wisconsin USA.
  • Ances BM; Department of Medical & Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA.
  • Wang MC; Department of Neurology, Massachusetts General Hospital Harvard Medical School Charlestown Massachusetts USA.
  • Tycko B; Departments of Neurology and Radiology, Massachusetts General Hospital Harvard Medical School Charlestown Massachusetts USA.
  • Lee JH; Department of Psychiatry, School of Clinical Medicine University of Cambridge Cambridge UK.
  • O'Bryant S; Cambridgeshire and Peterborough NHS Foundation Trust Fulbourn Hospital Cambridge UK.
Alzheimers Dement (Amst) ; 12(1): e12039, 2020.
Article de En | MEDLINE | ID: mdl-32626817
ABSTRACT

INTRODUCTION:

Previously generated serum and plasma proteomic profiles were examined among adults with Down syndrome (DS) to determine whether these profiles could discriminate those with mild cognitive impairment (MCI-DS) and Alzheimer's disease (DS-AD) from those cognitively stable (CS).

METHODS:

Data were analyzed on n = 305 (n = 225 CS; n = 44 MCI-DS; n = 36 DS-AD) enrolled in the Alzheimer's Biomarker Consortium-Down Syndrome (ABC-DS).

RESULTS:

Distinguishing MCI-DS from CS, the serum profile produced an area under the curve (AUC) = 0.95 (sensitivity [SN] = 0.91; specificity [SP] = 0.99) and an AUC = 0.98 (SN = 0.96; SP = 0.97) for plasma when using an optimized cut-off score. Distinguishing DS-AD from CS, the serum profile produced an AUC = 0.93 (SN = 0.81; SP = 0.99) and an AUC = 0.95 (SN = 0.86; SP = 1.0) for plasma when using an optimized cut-off score. AUC remained unchanged to slightly improved when age and sex were included. Eotaxin3, interleukin (IL)-10, C-reactive protein, IL-18, serum amyloid A , and FABP3 correlated fractions at r2 > = 0.90.

DISCUSSION:

Proteomic profiles showed excellent detection accuracy for MCI-DS and DS-AD.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Alzheimers Dement (Amst) Année: 2020 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Alzheimers Dement (Amst) Année: 2020 Type de document: Article