APOE associated hemispheric asymmetry of entorhinal cortical thickness in aging and Alzheimer's disease
详细信息 查看全文
- 作者：Markus Donix ; Alison C. Burggren ; Maria Scharf ; Kira Marschner ; Nanthia A. Suthana ; Prabha Siddarth ; Allison K. Krupa ; Michael Jones ; Laurel Martin-Harris ; Linda M. Ercoli ; Karen J. Miller ; Annett Werner ; R眉diger von Kummer ; Cathrin Sauer ; Gary W. Small ; Vjera A. Holthoff ; Susan Y. Bookheimer
- 关键词：Entorhinal cortex ; Hippocampus ; Magnetic resonance imaging ; Cortical unfolding ; APOE-4 allele
- 刊名：Psychiatry Research: Neuroimaging
- 出版年：30 December, 2013
- 年：2013
- 卷：214
- 期：3
- 页码：212-220
- 全文大小：805 K
文摘
Across species structural and functional hemispheric asymmetry is a fundamental feature of the brain. Environmental and genetic factors determine this asymmetry during brain development and modulate its interaction with brain disorders. The e4 allele of the apolipoprotein E gene (APOE-4) is a risk factor for Alzheimer's disease, associated with regionally specific effects on brain morphology and function during the life span. Furthermore, entorhinal and hippocampal hemispheric asymmetry could be modified by pathology during Alzheimer's disease development. Using high-resolution magnetic resonance imaging and a cortical unfolding technique we investigated whether carrying the APOE-4 allele influences hemispheric asymmetry in the entorhinal cortex and the hippocampus among patients with Alzheimer's disease as well as in middle-aged and older cognitively healthy individuals. APOE-4 carriers showed a thinner entorhinal cortex in the left hemisphere when compared with the right hemisphere across all participants. Non-carriers of the allele showed this asymmetry only in the patient group. Cortical thickness in the hippocampus did not vary between hemispheres among APOE-4 allele carriers and non-carriers. The APOE-4 allele modulates hemispheric asymmetry in entorhinal cortical thickness. Among Alzheimer's disease patients, this asymmetry might be less dependent on the APOE genotype and a more general marker of incipient disease pathology.