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Defining SNAP by cross-sectional and longitudinal definitions of neurodegeneration

Wisse, L E M LU orcid ; Das, S R ; Davatzikos, C ; Dickerson, B C ; Xie, S X ; Yushkevich, P A and Wolk, D A (2018) In NeuroImage: Clinical 18. p.407-412
Abstract

INTRODUCTION: Suspected non-Alzheimer's pathophysiology (SNAP) is a biomarker driven designation that represents a heterogeneous group in terms of etiology and prognosis. SNAP has only been identified by cross-sectional neurodegeneration measures, whereas longitudinal measures might better reflect "active" neurodegeneration and might be more tightly linked to prognosis. We compare neurodegeneration defined by cross-sectional 'hippocampal volume' only (SNAP/L-) versus both cross-sectional and longitudinal 'hippocampal atrophy rate' (SNAP/L+) and investigate how these definitions impact prevalence and the clinical and biomarker profile of SNAP in Mild Cognitive Impairment (MCI).

METHODS: 276 MCI patients from ADNI-GO/2 were... (More)

INTRODUCTION: Suspected non-Alzheimer's pathophysiology (SNAP) is a biomarker driven designation that represents a heterogeneous group in terms of etiology and prognosis. SNAP has only been identified by cross-sectional neurodegeneration measures, whereas longitudinal measures might better reflect "active" neurodegeneration and might be more tightly linked to prognosis. We compare neurodegeneration defined by cross-sectional 'hippocampal volume' only (SNAP/L-) versus both cross-sectional and longitudinal 'hippocampal atrophy rate' (SNAP/L+) and investigate how these definitions impact prevalence and the clinical and biomarker profile of SNAP in Mild Cognitive Impairment (MCI).

METHODS: 276 MCI patients from ADNI-GO/2 were designated amyloid "positive" (A+) or "negative" (A-) based on their florbetapir scan and neurodegeneration 'positive' or 'negative' based on cross-sectional hippocampal volume and longitudinal hippocampal atrophy rate.

RESULTS: 74.1% of all SNAP participants defined by the cross-sectional definition of neurodegeneration also met the longitudinal definition of neurodegeneration, whereas 25.9% did not. SNAP/L+ displayed larger white matter hyperintensity volume, a higher conversion rate to dementia over 5 years and a steeper decline on cognitive tasks compared to SNAP/L- and the A- CN group. SNAP/L- had more abnormal values on neuroimaging markers and worse performance on cognitive tasks than the A- CN group, but did not show a difference in dementia conversion rate or longitudinal cognition.

DISCUSSION: Using a longitudinal definition of neurodegeneration in addition to a cross-sectional one identifies SNAP participants with significant cognitive decline and a worse clinical prognosis for which cerebrovascular disease may be an important driver.

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author
; ; ; ; ; and
author collaboration
publishing date
type
Contribution to journal
publication status
published
keywords
Aged, Aged, 80 and over, Aniline Compounds, Biomarkers, Cognitive Dysfunction/diagnostic imaging, Cross-Sectional Studies, Ethylene Glycols, Female, Hippocampus/diagnostic imaging, Humans, Image Processing, Computer-Assisted, Longitudinal Studies, Magnetic Resonance Imaging, Male, Mental Status Schedule, Middle Aged, Neurodegenerative Diseases/complications, Neuropsychological Tests
in
NeuroImage: Clinical
volume
18
pages
6 pages
publisher
Elsevier
external identifiers
  • scopus:85041746990
  • pmid:29487798
ISSN
2213-1582
DOI
10.1016/j.nicl.2018.02.008
language
English
LU publication?
no
id
ef76976d-9d40-493a-9165-a4aaa210c655
date added to LUP
2024-02-28 14:48:42
date last changed
2025-06-11 05:00:37
@article{ef76976d-9d40-493a-9165-a4aaa210c655,
  abstract     = {{<p>INTRODUCTION: Suspected non-Alzheimer's pathophysiology (SNAP) is a biomarker driven designation that represents a heterogeneous group in terms of etiology and prognosis. SNAP has only been identified by cross-sectional neurodegeneration measures, whereas longitudinal measures might better reflect "active" neurodegeneration and might be more tightly linked to prognosis. We compare neurodegeneration defined by cross-sectional 'hippocampal volume' only (SNAP/L-) versus both cross-sectional and longitudinal 'hippocampal atrophy rate' (SNAP/L+) and investigate how these definitions impact prevalence and the clinical and biomarker profile of SNAP in Mild Cognitive Impairment (MCI).</p><p>METHODS: 276 MCI patients from ADNI-GO/2 were designated amyloid "positive" (A+) or "negative" (A-) based on their florbetapir scan and neurodegeneration 'positive' or 'negative' based on cross-sectional hippocampal volume and longitudinal hippocampal atrophy rate.</p><p>RESULTS: 74.1% of all SNAP participants defined by the cross-sectional definition of neurodegeneration also met the longitudinal definition of neurodegeneration, whereas 25.9% did not. SNAP/L+ displayed larger white matter hyperintensity volume, a higher conversion rate to dementia over 5 years and a steeper decline on cognitive tasks compared to SNAP/L- and the A- CN group. SNAP/L- had more abnormal values on neuroimaging markers and worse performance on cognitive tasks than the A- CN group, but did not show a difference in dementia conversion rate or longitudinal cognition.</p><p>DISCUSSION: Using a longitudinal definition of neurodegeneration in addition to a cross-sectional one identifies SNAP participants with significant cognitive decline and a worse clinical prognosis for which cerebrovascular disease may be an important driver.</p>}},
  author       = {{Wisse, L E M and Das, S R and Davatzikos, C and Dickerson, B C and Xie, S X and Yushkevich, P A and Wolk, D A}},
  issn         = {{2213-1582}},
  keywords     = {{Aged; Aged, 80 and over; Aniline Compounds; Biomarkers; Cognitive Dysfunction/diagnostic imaging; Cross-Sectional Studies; Ethylene Glycols; Female; Hippocampus/diagnostic imaging; Humans; Image Processing, Computer-Assisted; Longitudinal Studies; Magnetic Resonance Imaging; Male; Mental Status Schedule; Middle Aged; Neurodegenerative Diseases/complications; Neuropsychological Tests}},
  language     = {{eng}},
  pages        = {{407--412}},
  publisher    = {{Elsevier}},
  series       = {{NeuroImage: Clinical}},
  title        = {{Defining SNAP by cross-sectional and longitudinal definitions of neurodegeneration}},
  url          = {{http://dx.doi.org/10.1016/j.nicl.2018.02.008}},
  doi          = {{10.1016/j.nicl.2018.02.008}},
  volume       = {{18}},
  year         = {{2018}},
}