4.5 Article

Brain MRI after critical care admission: A longitudinal imaging study

期刊

JOURNAL OF CRITICAL CARE
卷 62, 期 -, 页码 117-123

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.jcrc.2020.11.024

关键词

AD-signature cortex; Cortical thinning; Corpus callosum; Hippocampus; Magnetic resonance imaging; Intensive care unit; Older adults

资金

  1. NIH [P50 AG016574, P30 AG062677, U01 AG006786, R01 AG034676, R01 AG41851, R37 AG11378]
  2. Elsie and Marvin Dekelboum Family Foundation
  3. GHR Foundation
  4. Alexander Family Alzheimer's Disease Research Professorship of the Mayo Clinic, Liston Award
  5. Alzheimer's Association
  6. Schuler Foundation
  7. Mayo Foundation for Medical Education and Research
  8. Rochester Epidemiology Project [R01 AG034676]
  9. Mayo Clinic Center for Clinical and Translational Science (CTSA)
  10. National Center for Advancing Translational Sciences (NCATS) [UL1 TR000135]

向作者/读者索取更多资源

The study found that critical care hospitalization in older adults is associated with accelerated brain atrophy in selected regions, but does not increase amyloid deposition, with more pronounced changes in delirium patients.
Purpose: To investigate the association between episodes of critical care hospitalizations and delirium with structural brain changes in older adults. Materials and methods: We included Mayo Clinic Study of Aging participants >= 60 years old at the time of study enrollment (October 29, 2004, through September 11, 2017) with available brain MRI and 'amyloid' positron emission tomography (PET) scans. We tested the hypothesis that a) intensive care unit (ICU) admission is associated with greater cortical thinning and atrophy in entorhinal cortex, inferior temporal cortex, middle temporal cortex, and fusiform cortex (Alzheimer''s disease-signature regions); b) atrophy in hippocampus and corpus callosum; c) delirium accelerates these changes; and d) ICU admission is not associated with increased deposition of cortical amyloid. Results: ICU admission was associated with cortical thinning in temporal, frontal, and parietal cortices, and decreases in hippocampal/corpus callosum volumes, but not Alzheimer''s disease-signature regions. For hippocampal volume, and 10 of 14 cortical thickness measurements, the change following ICU admission was significantly more pronounced for those who experienced delirium. ICU admission was not associated with an increased amyloid burden. Conclusions: Critical care hospitalization is associated with accelerated brain atrophy in selected brain regions, without increases in amyloid deposition, suggesting a pathogenesis based on neurodegeneration unrelated to Alzheimer''s pathway. (c) 2020 Elsevier Inc. All rights reserved.

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