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February 1, 1998Stroke310 citations

Relationship Between ApoE, MRI Findings, and Cognitive Function in the Cardiovascular Health Study

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LKLewis H. KullerLSLynn ShemanskiTMTeri A. Manolio

Key Result

ApoE-4 genotype (OR 1.6; 95% CI 1.1-2.1), high ventricular volume, high white matter grade, and infarctlike lesions were significantly associated with low cognitive scores.

Key Points

  • The aim was to explore the relationship between ApoE, MRI findings, and cognitive function in older adults.
  • Evaluated 3469 participants from the Cardiovascular Health Study over 3 years.
  • Assessed ApoE genotype, MRI brain examinations, and cognitive scores using the 3MSE.
  • Analyzed the impact of age, education, and cardiovascular history on cognitive performance.
  • Prevalence of low 3MSE scores was 20.4% among participants with stroke history versus 8.2% without.
  • ApoE-4 presence and high ventricular volume significantly increased the odds of low cognitive scores (OR, 1.6).
  • Participants with multiple risk factors (low education, older age, incident stroke) showed a greater decline in scores over time.

Study Design

Type

Cohort (n=3,469)

Structured PICO

Are ApoE genotype and brain MRI findings associated with low cognitive scores and cognitive decline in older adults?

P
Population
3,469 black and white participants in the Cardiovascular Health Study (CHS) evaluated in years 5 and 6
O
Outcome
Low (<80) score on the Modified Mini-Mental State Examination (3MSE)surrogate

Vascular changes on MRI, brain atrophy, and ApoE-4 genotype are significantly associated with low cognitive scores and cognitive decline in older adults.

Main Result

Effect estimate: OR 1.6 (95% CI 1.1 to 2.1)

Abstract

BACKGROUND AND PURPOSE: We determined the relationship between apolipoprotein (Apo)E, MRI, and low cognitive scores. METHODS: The relationship between age, education, ApoE genotype, MRI examination of the brain, subclinical and clinical cardiovascular disease, and low (<80) score on the Modified Mini-Mental State Examination (3MSE, as modified by Teng and Chui) was evaluated for 3469 black and white participants in the Cardiovascular Health Study (CHS) in years 5 and 6 of the study. The participants were followed for up to 3 years. RESULTS: The prevalence of scores <80 in years 5 and 6 of the CHS was 8.2% for participants without and 20.4% for those with prior history of stroke. Age, race, and education were important determinants of low 3MSE scores. The prevalence of ApoE-4 (odds ratio OR, 1.6 1.1 to 2.1) was directly related to scores <80, as was high ventricular volume (OR, 1.6 1.2 to 2.3), high white matter grade (OR, 1.4 1.1 to 1.9), and infarctlike lesions (OR, 1.6 1.2 to 2.1) on the MRI in the multivariate analysis. A five-point or greater decline in scores over up to 3 years was more often observed for participants with low 3MSE scores at year 5, at older ages, with lower education, and experiencing incident stroke (OR, 3.6 1.2 to 10.6), ApoE-4 genotype (OR, 1.8 1.4 to 2.3), and with MRI findings of high ventricular volume (OR, 2.0 1.5 to 2.7), and infarctlike lesions (OR, 1.2 0.9 to 1.5). CONCLUSIONS: These results demonstrate that vascular changes on MRI, measures of brain atrophy, ApoE-4, and age, education, and race are associated with low cognitive scores among older individuals. The MRI of the brain provides valuable information related to cognitive tests and decline over time. The potential exists for using MRI measurements to identify high-risk individuals for dementia and to test potential interventions to reduce the risk of dementia.

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Cite This Study

Kuller et al. (1998) conducted a cohort in Low cognitive scores (n=3,469). ApoE genotype and MRI findings was evaluated on Low (<80) score on the Modified Mini-Mental State Examination (3MSE) (OR 1.6, 95% CI 1.1 to 2.1). ApoE-4 genotype (OR 1.6; 95% CI 1.1-2.1), high ventricular volume, high white matter grade, and infarctlike lesions were significantly associated with low cognitive scores.

synapsesocial.com/papers/6a0ede29218372ada647cacehttps://doi.org/10.1161/01.str.29.2.388
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