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ATN cerebrospinal fluid biomarkers in dementia with Lewy bodies: Initial results from the United States Dementia with Lewy Bodies Consortium.
Jain, Lavanya; Khrestian, Maria; Formica, Shane; Tuason, Elizabeth D; Pillai, Jagan A; Rao, Stephen; Oguh, Odinachi; Lippa, Carol F; Lopez, Oscar L; Berman, Sarah B; Tsuang, Debby W; Zabetian, Cyrus P; Irwin, David J; Galasko, Douglas R; Litvan, Irene; Marder, Karen S; Honig, Lawrence S; Fleisher, Jori E; Galvin, James E; Bozoki, Andrea C; Taylor, Angela S; Sabbagh, Marwan N; Leverenz, James B; Bekris, Lynn M.
Affiliation
  • Jain L; Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Khrestian M; Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Formica S; Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Tuason ED; Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Pillai JA; Cleveland Clinic Lou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, Ohio, USA.
  • Rao S; Cleveland Clinic Lou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, Ohio, USA.
  • Oguh O; Cleveland Clinic Lou Ruvo Center for Brain Health-Las Vegas, Cleveland Clinic, Las Vegas, Nevada, USA.
  • Lippa CF; Cleveland Clinic Lou Ruvo Center for Brain Health-Las Vegas, Cleveland Clinic, Las Vegas, Nevada, USA.
  • Lopez OL; Cognitive Disorders & Comprehensive Alzheimer's Disease Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Berman SB; Department of Neurology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Tsuang DW; Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, Washington, USA.
  • Zabetian CP; Geriatric Research, Education, and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, USA.
  • Irwin DJ; Geriatric Research, Education, and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, USA.
  • Galasko DR; Department of Neurology, University of Washington School of Medicine, Seattle, Washington, USA.
  • Litvan I; Department of Neurology, University of Pennsylvania Health System, Philadelphia, Pennsylvania, USA.
  • Marder KS; Digital Neuropathology Laboratory, Philadelphia, Pennsylvania, USA.
  • Honig LS; Lewy Body Disease Research Center of Excellence, Philadelphia, Pennsylvania, USA.
  • Fleisher JE; Frontotemporal Degeneration Center, Philadelphia, Pennsylvania, USA.
  • Galvin JE; Department of Neurosciences, University of California, San Diego, California, USA.
  • Bozoki AC; Department of Neurosciences, University of California, San Diego, California, USA.
  • Taylor AS; Columbia University Irving Medical Center, New York, New York, USA.
  • Sabbagh MN; Department of Neurosciences, University of California, San Diego, California, USA.
  • Leverenz JB; Department of Neurological Sciences, Rush Medical College, Chicago, Illinois, USA.
  • Bekris LM; Department of Neurology, Comprehensive Center for Brain Health, University of Miami Miller School of Medicine, Miami, Florida, USA.
Alzheimers Dement ; 20(1): 549-562, 2024 Jan.
Article in En | MEDLINE | ID: mdl-37740924
ABSTRACT

INTRODUCTION:

The National Institute on Aging - Alzheimer's Association (NIA-AA) ATN research framework proposes to use biomarkers for amyloid (A), tau (T), and neurodegeneration (N) to stage individuals with AD pathological features and track changes longitudinally. The overall aim was to utilize this framework to characterize pre-mortem ATN status longitudinally in a clinically diagnosed cohort of dementia with Lewy bodies (DLB) and to correlate it with the post mortem diagnosis.

METHODS:

The cohort was subtyped by cerebrospinal fluid (CSF) ATN category. A subcohort had longitudinal data, and a subgroup was neuropathologically evaluated.

RESULTS:

We observed a significant difference in Aß42/40 after 12 months in the A+T- group. Post mortem neuropathologic analyses indicated that most of the p-Tau 181 positive (T+) cases also had a high Braak stage.

DISCUSSION:

This suggests that DLB patients who are A+ but T- may need to be monitored to determine whether they remain A+ or ever progress to T positivity. HIGHLIGHTS Some A+T- DLB subjects transition from A+ to negative after 12-months. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Monitoring of the A+T- sub-type of DLB may be necessary.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lewy Body Disease / Alzheimer Disease Limits: Humans Language: En Journal: Alzheimers Dement Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lewy Body Disease / Alzheimer Disease Limits: Humans Language: En Journal: Alzheimers Dement Year: 2024 Type: Article Affiliation country: United States