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Cerebral Hemodynamic Impairment and Cognitive Dysfunction in APOE4 Carriers With Asymptomatic Carotid Artery
Yoshinori Kakino1, Yorito Hattori1,2, Soshiro Ogata3
1Department of Neurology National Cerebral and Cardiovascular Center Suita, Osaka Japan.
Insights
The presence of the APOE4 gene increases the risk of reduced cerebral blood flow and memory deficits in individuals with asymptomatic carotid artery stenosis or occlusion. APOE genotyping can aid in early disease severity detection.
Area of Science:
- Neuroscience
- Genetics
- Vascular Medicine
Background:
- Previous preclinical studies indicated that APOE4-targeted replacement mice show more severe cerebral hypoperfusion and cognitive impairment than APOE3-targeted replacement mice with carotid artery stenosis.
- Neurovascular dysfunction is a key factor in the observed impairments.
Purpose of the Study:
- To clinically investigate the contribution of the APOE4 genotype to cerebral hemodynamic and cognitive impairment in patients with asymptomatic carotid artery stenosis or occlusion.
Main Methods:
- A cross-sectional observational study was conducted from January 2017 to March 2022.
- Included 91 subjects (primary analysis) and 161 subjects (sensitivity analysis) with asymptomatic carotid artery stenosis or occlusion.
- Neuropsychological examinations and 15O-gas positron emission tomography were utilized to assess cognitive function and cerebral blood flow.
Main Results:
- APOE4 was identified as an independent risk factor for reduced cerebral blood flow in the anterior circulation territory (primary analysis: β=-0.058, P=0.005; sensitivity analysis: β=-0.048, P=0.003).
- APOE4 carriers also exhibited short-term memory impairment (Alzheimer's Disease Assessment Scale-Cognitive Subscale 13: β=1.16, P=0.048).
- In the primary analysis, 22.0% of subjects were APOE4 carriers; in the sensitivity analysis, 19.3% were carriers.
Conclusions:
- The APOE4 genotype may increase the risk of decreased cerebral blood flow and associated memory impairment in individuals with asymptomatic carotid artery stenosis or occlusion.
- APOE genotyping could be beneficial for the early detection of disease severity in these patients.
Background:
Our previous preclinical study demonstrated that APOE4-targeted replacement mice exhibit more severe cerebral hypoperfusion and cognitive impairment than APOE3-targeted replacement mice with carotid artery stenosis due to neurovascular dysfunction. Therefore, we clinically investigate whether APOE4 contributes to cerebral hemodynamic and cognitive impairment in subjects with asymptomatic carotid artery stenosis or occlusion.
Methods And Results:
A cross-sectional observational study was conducted between January 2017 and March 2022. In a primary analysis, 91 subjects (114 affected cerebral hemispheres) with asymptomatic carotid artery stenosis or occlusion who underwent neuropsychological examinations and 15O-gas positron emission tomography were included to examine associations of APOE4 with cognitive impairment and cerebral hemodynamic impairment. A sensitivity analysis was performed with 161 subjects (201 affected cerebral hemispheres) who underwent 15O-gas positron emission tomography scan. In the primary analysis, 20 (22.0%) subjects were APOE4 carriers. APOE4 was an independent risk factor of lower cerebral blood flow in the anterior circulation territory (β=-0.058 [95% CI, -0.098 to -0.018], P=0.005) and short-term memory impairment in Alzheimer's Disease Assessment Scale-Cognitive Subscale 13 (β=1.16 [95% CI, 0.009-2.30], P=0.048) in a multivariable linear regression analysis. In the sensitivity analysis, 31 (19.3%) subjects carried APOE4, which was an independent risk factor of lower cerebral blood flow (β=-0.048 [95% CI, -0.079 to -0.012], P=0.003) in the anterior circulation territory.
Conclusions:
APOE4 may confer an increased risk of decreased cerebral blood flow accompanied by memory impairment in asymptomatic carotid artery stenosis or occlusion consistent with our experimental study. APOE genotyping in such subjects may be useful for early detection of disease severity.
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