Intracranial volume in mild cognitive impairment, Alzheimer's disease and vascular dementia: evidence for brain reserve?

Objective The possibility of brain volume reserve effects was examined in a sample of geriatric outpatients with mild cognitive impairment (MCI), Alzheimer's disease (AD) and vascular dementia (VaD). The total intracranial volume (ICV) served as an estimate of the maximum attained brain volume...

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Published inInternational journal of geriatric psychiatry Vol. 19; no. 10; pp. 995 - 1007
Main Authors Wolf, Henrike, Julin, Per, Gertz, Hermann-Josef, Winblad, Bengt, Wahlund, Lars-Olof
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.10.2004
Wiley
Wiley Subscription Services, Inc
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ISSN0885-6230
1099-1166
DOI10.1002/gps.1205

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Summary:Objective The possibility of brain volume reserve effects was examined in a sample of geriatric outpatients with mild cognitive impairment (MCI), Alzheimer's disease (AD) and vascular dementia (VaD). The total intracranial volume (ICV) served as an estimate of the maximum attained brain volume in life. Methods Subjects (n = 181, mean age 60.7) were consecutive referrals to a geriatric outpatients clinic (n = 96) and a group of age‐matched healthy control subjects (n = 85). ICV and brain volume were attained from T1‐weighted magnetic resonance images using a stereological method. Hippocampal atrophy was assessed with a visual rating scale. Results ICV was significantly smaller in patients with AD and VaD than in control subjects, but effect size was small. After adjusting for age and gender, having ICV in the smallest quartile significantly increased the risk of cognitive impairment (either MCI or dementia). In patients with dementia, but not in MCI, severity of cognitive impairment and ICV were moderately correlated. The effect of ICV on cognition was not mediated by hippocampal atrophy. Conclusions These findings are compatible with volume reserve effects that modify the clinical expression of symptoms in both AD and VaD. They may have implications for the design of neuroimaging studies that use ICV for normalization procedures. Copyright © 2004 John Wiley & Sons, Ltd.
Bibliography:Deutsche Forschungsgemeinschaft (DFG)
istex:9C30FD5EF08D9C65E332F5B8263D72B966E1338B
Gun-och Bertil Stohne Stiftelse (Sweden)
ark:/67375/WNG-ZLP45K7D-J
Hans and Loo Ostermans Research Fund (Neurotec, Huddinge)
Interdisziplinäres Zentrum für Klinische Forschung (IZKF, Projekt C8, Dept of Psychiatry, University of Leipzig)
ArticleID:GPS1205
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ISSN:0885-6230
1099-1166
DOI:10.1002/gps.1205