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Apolipoproteins E and C1 and brain morphology in memory impaired elders.
- Source :
-
Neurogenetics [Neurogenetics] 2003 Apr; Vol. 4 (3), pp. 141-6. Date of Electronic Publication: 2002 Dec 21. - Publication Year :
- 2003
-
Abstract
- Previous research has shown that polymorphisms of the apolipoproteins E ( APOE) and APOC1 represent genetic risk factors for dementia and for cognitive impairment in the elderly. The brain mechanisms by which these genetic variations affect behavior or clinical severity are poorly understood. We studied the effect of APOE and APOC1 genes on magnetic resonance imaging measures in a sample of 50 subjects with age-associated memory impairment. The APOE E4 allele was associated with reduced left hippocampal volumes and APOE*E3 status was associated with greater frontal lobe white matter volumes. However, no APOE effects were observed when analyses accounted for other potential confounding variables. The effects of APOC1 on hippocampal volumes appeared to be more robust than those of the APOE polymorphism. However, no modulatory effects on brain morphology outside the medial temporal lobe region were observed when demographic variables, clinical status, and other anatomical brain measurements were taken into consideration. Our results suggest that the role of the APOC1 polymorphism in brain morphology of the cognitively impaired elderly should be examined in further studies.
- Subjects :
- Aged
Aging pathology
Alleles
Apolipoprotein C-I
Apolipoprotein E2
Apolipoprotein E3
Apolipoprotein E4
Apolipoproteins C physiology
Apolipoproteins E physiology
Cephalometry
Cerebral Ventricles pathology
Confounding Factors, Epidemiologic
Female
Frontal Lobe pathology
Genetic Predisposition to Disease
Genotype
Hippocampus pathology
Humans
Magnetic Resonance Imaging
Male
Neuropsychological Tests
Temporal Lobe pathology
Verbal Learning
Aging psychology
Apolipoproteins C genetics
Apolipoproteins E genetics
Brain pathology
Memory Disorders pathology
Polymorphism, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1364-6745
- Volume :
- 4
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Neurogenetics
- Publication Type :
- Academic Journal
- Accession number :
- 12736801
- Full Text :
- https://doi.org/10.1007/s10048-002-0142-8