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Reduced hippocampal volume in non-demented carriers fo the apolipoprotein E ε4 : Relation to chronological age and recognition memory

Lind, Johanna (author)
Karolinska Institutet
Larsson, Anne (author)
Umeå universitet,Radiofysik
Persson, Jonas (author)
Umeå universitet,Institutionen för psykologi,Department of Psychology, University of Michigan, Ann Arbor, MI 48109, USA
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Ingvar, Martin (author)
Karolinska Institutet
Nilsson, Lars-Göran (author)
Stockholms universitet,Psykologiska institutionen
Bäckman, Lars (author)
Karolinska Institutet
Adolfsson, Rolf (author)
Umeå universitet,Psykiatri
Cruts, Marc (author)
Department of Molecular Genetics, Flanders Interuniversity, Institute of Biotechnology, University of Antwerp, B-2610 Antwerpen, Belgium
Sleegers, Kristel (author)
Department of Molecular Genetics VIB8, University of Antwerp, Campus CDE, Universiteitsplein 1, B-2610 Antwerp, Belgium
Van Broeckhoven, Christine (author)
Department of Molecular Genetics, Flanders Interuniversity, Institute of Biotechnology, University of Antwerp, B-2610 Antwerpen, Belgium
Nyberg, Lars, 1966- (author)
Umeå universitet,Institutionen för psykologi
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 (creator_code:org_t)
Elsevier BV, 2006
2006
English.
In: Neuroscience Letters. - : Elsevier BV. - 0304-3940 .- 1872-7972. ; 396:1, s. 23-27
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Apolipoprotein E ε4 (APOE ε4) is the main known genetic risk factor for Alzheimer's disease (AD). Some previous studies have reported structural brain changes as well as cognitive deficits in non-demented APOE ε4 carriers, but the pattern of results is inconsistent and studies with larger sample sizes have been called for. Here we compared hippocampal volume and recognition–memory performance between AD-symptom-free carriers (N = 30) and non-carriers (N = 30) of the APOE ε4 (age range: 49–79 years). We observed reduced right hippocampal volume in APOE ε4 carriers, and found that the difference was most pronounced before the age of 65. Further, the APOE ε4 carriers made significantly more false alarms in the recognition–memory test, and the number of false alarms correlated significantly with right hippocampus volume. These results indicate that relatively young individuals at genetic risk for AD have smaller hippocampal volume and lower performance on hippocampal-dependent cognitive tasks. A question for the future is whether smaller hippocampal volume represents early-onset hippocampal volume reduction or an inherent trait.

Subject headings

SAMHÄLLSVETENSKAP  -- Psykologi (hsv//swe)
SOCIAL SCIENCES  -- Psychology (hsv//eng)

Keyword

Alzheimer's disease
APOE
MRI
Memory
Hippocampus
Psychology

Publication and Content Type

ref (subject category)
art (subject category)

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