Stroke and apolipoprotein E epsilon 4 are independent risk factors for cognitive decline - A population-based study

Citation
Mg. Dik et al., Stroke and apolipoprotein E epsilon 4 are independent risk factors for cognitive decline - A population-based study, STROKE, 31(10), 2000, pp. 2431-2436
Citations number
37
Categorie Soggetti
Neurology,"Cardiovascular & Hematology Research
Journal title
STROKE
ISSN journal
00392499 → ACNP
Volume
31
Issue
10
Year of publication
2000
Pages
2431 - 2436
Database
ISI
SICI code
0039-2499(200010)31:10<2431:SAAEE4>2.0.ZU;2-2
Abstract
Background and Purpose-Stroke and apolipoprotein E epsilon 4 (ApoE epsilon 4) are individually important risk factors for cognitive decline, including Alzheimer disease. It has been suggested that ApoE epsilon 4 multiplies th e risk for cognitive decline following stroke. In a population-based sample , using well-defined sensitive cognitive measures, this study investigates whether cognitive decline following stroke is worse for patients who carry the ApoE epsilon 4 allele. Methods-Subjects were participants in the Longitudinal Aging Study Amsterda m (LASA). The sample consisted of 1224 subjects, aged 62 to 85 years, who p articipated in the 3-year follow-up examination and for whom ApoE and strok e data were complete. We assessed cognitive decline using the Mini-Mental S tate Examination, the Auditory Verbal Learning Test (memory: immediate and delayed recall), and the Coding Task (information processing speed). The ef fects of stroke and ApoE epsilon 4 on cognitive decline were evaluated with ANOVA and multiple logistic regression analysis, adjusted for age, sex, ed ucation, and baseline cognition. Results-A synergistic effect modification for stroke and ApoE epsilon 4 on cognitive decline was not observed. Unexpectedly, instead, stroke patients canying the epsilon 4 allele demonstrated a nonsignificantly lowered risk f or Mini-Mental State Examination decline (R = 0.3; 95% CI 0.1 to 1.1). ApoE epsilon 4 was associated with declines in information processing speed (OR =1,5; 95% CI 1.1 to 2.1) and small declines for immediate and delayed recal l. Conclusions-Stroke and ApoE epsilon 4 may impair cognition through distinct nonsynergistic mechanisms. The slowing of information processing speed for ApoE epsilon 4 carriers was more evident than impairment in memory.