Does APO ε4 correlate with MRI changes in Alzheimer's disease?

24Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

Abstract

Objective - To assess the relation between APO E genotype and MRI white matter changes in Alzheimer's disease. The APO ε4 allele is correlated with amyloid angiopathy and other neuropathologies in Alzheimer's disease and could be associated with white matter changes. If so, there should be a dose effect. Methods - 104 patients with probable Alzheimer's disease (NINCDS-ADRDA criteria) in this Alzheimer's Disease Research Centre were studied. Patients received MRI and APO E genotyping by standardised protocols. Axial MRI was scored (modified Schelten's scale) for the presence and degree of white matter changes and atrophy in several regions by a neuroradiologist blinded to genotype. Total white matter and total atrophy scores were also generated. Data analysis included Pearson's correlation for regional and total imaging scores and analysis of variance (ANOVA) (or Kruskal-Wallis) and X2 for demographic and disease related variables. Results - 30 patients had no ε4, 53 patients were heterozygous, and 21 patients were homozygous. The three groups did not differ in sex distribution, age of onset, age at MRI, MMSE, clinical dementia rating, or modified Hachinski ischaemia scores. There were no significant correlations between total or regional white matter scores and APO E genotype (Pearson correlation). Conclusions - No correlation between total or regional white matter scores and APO E genotype was found. The pathogenesis of white matter changes in Alzheimer's disease may be independent of APO E genotype.

Cite

CITATION STYLE

APA

Doody, R. S., Azher, S. N., Haykal, H. A., Dunn, J. K., Liao, T., & Schneider, L. (2000). Does APO ε4 correlate with MRI changes in Alzheimer’s disease? Journal of Neurology Neurosurgery and Psychiatry, 69(5), 668–671. https://doi.org/10.1136/jnnp.69.5.668

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free