Cited by 44Dementia and Cognitive Impairment ResearchIntensive Care Unit Cognitive DisordersLong-Term Effects of COVID-19

The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.

Association of hospitalization with long-term cognitive and brain MRI changes in the ARIC cohort

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Abstract

OBJECTIVE: To determine whether hospitalization is associated with subsequent cognitive decline or changes on brain MRI in a community-based cohort. METHODS: Baseline and follow-up cognitive testing (n = 2,386) and MRI scans with standardized assessments (n = 885) were available from a subset of white and black participants in the Atherosclerosis Risk in Communities study. Cognitive tests included the Delayed Word Recall Test (DWRT), Digit Symbol Substitution Test (DSST), and Word Fluency Test (WFT). Hospitalization characteristics were determined using ICD-9 codes. Regression models adjusted for demographics, education, comorbidities, and APOE ε4 were used to estimate the independent association of hospitalization with changes in cognition or neuroimaging. RESULTS: Over a mean 14.1 years between visits, 1,266 participants (53.1%) were hospitalized. Hospitalization compared with no hospitalization was associated with greater decline in DSST scores (1.25 points greater decline, p < 0.001) but no difference in DWRT or WFT score change. Each additional hospitalization, as well as a critical illness vs noncritical illness hospitalization, was associated with greater decline in DSST scores. A subset of participants (n = 885) underwent MRI scans separated by 10.5 years. Hospitalization (n = 392) compared with no hospitalization was associated with a 57% higher odds of increasing ventricular size at follow-up. Each additional hospitalization, as well as having a critical illness vs noncritical illness hospitalization, and having a hospitalization with major surgery vs no surgery was associated with greater odds of increased ventricular size. CONCLUSIONS: Cognitive decline and neuroimaging changes may occur after hospitalization, independent of baseline demographics and comorbidities.

Overview

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Crossref · 10.1212/wnl.0000000000001439

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  1. Royston P. Multiple imputation using missing values: update. Stata J 2005;5:118–201.

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Metadata

Authors
Brown, C. H., Sharrett, A. R., Coresh, J., Schneider, A. L. C., Alonso, A., Knopman, D. S., Mosley, T. H., & Gottesman, R. F.
Affiliations
  • University of Minnesota (US)
  • From Johns Hopkins School of Medicine (C.H.B., A.L.C.S., R.F.G.), Johns Hopkins Bloomberg School of Public Health (A.R.S., J.C., A.L.C.S.), Baltimore, MD; University of Minnesota (A.A.), Minneapolis; Mayo Clinic (D.S.K.), Rochester, MN; and University of Mississippi Medical Center (T.H.M.), Jackson.
Venue
Neurology
Published
2015-04-07
Volume
84
Issue
14
Pages
1443-1453
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2154652580
Cited by
42
References
42
Citations by year
2026: 1 · 2025: 4 · 2024: 4 · 2023: 4 · 2022: 4 · 2021: 6 · 2020: 6 · 2019: 3 · 2018: 2 · 2017: 2 · 2016: 3 · 2015: 3
FWCI
2.71
Type
journal article
Language
en
Open access
Locations
  • Neurology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Eli Lilly and Company
  • H. Lundbeck A/S
  • National Institutes of Health (HHSN268201100012C, HHSN268201100008C, HHSN268201100006C, HHSN26820- 1100005C, HHSN268201100007C, 5u01hl096899-08, 5r01ag033615-05, HHSN268201100011C, HHSN268201100010C, HHSN268201100009C, 5u01hl096902-08, HHSN268200625226C, contract HHSN268200625226C)
  • U.S. Public Health Service (HHSN 268200625226C)
  • National Institute on Aging (R03AG042331, R01-AG033615, R01 AG033615-01A1)
  • National Heart, Lung, and Blood Institute (HHSN268201 100012C, HHSN268201100007I, HHSN268201100007C, R01 HL70825, U01HL075572, R01HL087641, R01HL59367 and R01HL086694, HHSN2682 01100008C, HH-SN-268201100006C, HHSN268201100011C, HHSN2682011-00005I, HL096814, HL096812, HHSN2682011-­00009I, R01 HL-59367, HHSN268201100005C, HHSN268201100005G, HHSN268201100010C, HHSN268201100011I, HHSN268200625226C, U01HL096814, U01-HL-096899, R01HL087641, HL-096902, R01HL059367, HHSN26820 1100009C, U01-HL-096902, HHSN2682011-00008I, HL-096899, U01HL096917, HL-096917, R01HL070825, T32HL007024, U01HL096812, R01HL086694, HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN268201100010C, HHSN268201100011C, HHSN268201100012C)
  • National Human Genome Research Institute (U01HG004402)
  • National Center for Research Resources (UL1RR025005)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Intensive Care Unit Cognitive Disorders
  • Health Sciences › Medicine › Clinical Neurology › Long-Term Effects of COVID-19
Keywords
hospitalization, cognitive decline, brain MRI, ventriculomegaly, critical illness, major surgery, Atherosclerosis Risk in Communities Study, APOE ε4, white matter changes
MeSH terms
Aged, Cerebral Ventricles, Cognition Disorders, Female, Follow-Up Studies, Hospitalization, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mississippi, Neuropsychological Tests, North Carolina, Time Factors

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