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Association of apolipoprotein E epsilon2 with white matter disease but not with microbleeds
Robin Lemmens1, Astrid Görner, Maarten Schrooten
1Department of Neurology, University Hospitals Leuven, Leuven, Belgium.
Background And Purpose:
Apolipoprotein E (apoE) alleles (epsilon2 and epsilon4) are associated with cerebral amyloid angiopathy, in which white matter disease and microbleeds are prominent features. The role of apoE in patients with microbleeds or white matter disease but no evidence of cerebral amyloid angiopathy has not been elucidated. We studied apoE alleles in relation to white matter disease and microbleeds in patients with transient ischemic attack or ischemic stroke.
Methods:
We obtained brain MRI scans and apoE genotypes in 334 transient ischemic attack or ischemic stroke patients. Microbleeds were scored on a gradient echo MRI and white matter disease was examined on fluid attenuated inversion recovery MRI using a semiquantitative rating scale.
Results:
Patients with moderate to severe white matter disease more frequently carried apoE epsilon2 alleles (25.2% versus 11.3%, P=0.001), but not apoE epsilon4 (26.6% in apoE epsilon4 carriers versus 25.9%; P=0.98). Adjustment for traditional risk factors did not modify this relationship (odds ratio, 2.9; 95% confidence interval, 1.5 to 5.3). There was no association between the presence of microbleeds and the apoE epsilon4 or apoE epsilon2 alleles.
Conclusions:
ApoE alleles do not exert a major influence on the development of microbleeds, but apoE epsilon2 may be associated with development of moderate to severe white matter disease in transient ischemic attack and stroke patients.
Insights
Apolipoprotein E (apoE) epsilon2 alleles are linked to white matter disease in stroke patients, but not microbleeds. ApoE epsilon4 showed no association with either condition in this study.
Area of Science:
- Neurology
- Genetics
- Vascular Disease
Background:
- Apolipoprotein E (apoE) alleles, specifically epsilon2 and epsilon4, are known risk factors for cerebral amyloid angiopathy.
- The association between apoE alleles and cerebrovascular conditions like white matter disease and microbleeds in patients without diagnosed cerebral amyloid angiopathy remains unclear.
Purpose of the Study:
- To investigate the relationship between apolipoprotein E (apoE) alleles and the presence of white matter disease and microbleeds.
- To examine apoE's role in patients experiencing transient ischemic attack (TIA) or ischemic stroke.
Main Methods:
- Brain MRI scans and apoE genotyping were performed on 334 patients with TIA or ischemic stroke.
- White matter disease was assessed using fluid attenuated inversion recovery (FLAIR) MRI, and microbleeds were quantified using gradient echo MRI.
Main Results:
- Apolipoprotein E (apoE) epsilon2 alleles were significantly more common in patients with moderate to severe white matter disease (25.2% vs. 11.3%, P=0.001).
- No significant association was found between apoE epsilon4 and white matter disease or microbleeds.
- The presence of microbleeds was not associated with either apoE epsilon2 or apoE epsilon4 alleles.
Conclusions:
- Apolipoprotein E (apoE) alleles do not appear to significantly influence the development of microbleeds.
- The apoE epsilon2 allele may be associated with the development of moderate to severe white matter disease in patients with transient ischemic attack and stroke.
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