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. 2019 Dec 10;93(24):e2257-e2271.
doi: 10.1212/WNL.0000000000008612. Epub 2019 Nov 11.

Profile of and risk factors for poststroke cognitive impairment in diverse ethnoregional groups

Collaborators, Affiliations

Profile of and risk factors for poststroke cognitive impairment in diverse ethnoregional groups

Jessica W Lo et al. Neurology. .

Abstract

Objective: To address the variability in prevalence estimates and inconsistencies in potential risk factors for poststroke cognitive impairment (PSCI) using a standardized approach and individual participant data (IPD) from international cohorts in the Stroke and Cognition Consortium (STROKOG) consortium.

Methods: We harmonized data from 13 studies based in 8 countries. Neuropsychological test scores 2 to 6 months after stroke or TIA and appropriate normative data were used to calculate standardized cognitive domain scores. Domain-specific impairment was based on percentile cutoffs from normative groups, and associations between domain scores and risk factors were examined with 1-stage IPD meta-analysis.

Results: In a combined sample of 3,146 participants admitted to hospital for stroke (97%) or TIA (3%), 44% were impaired in global cognition and 30% to 35% were impaired in individual domains 2 to 6 months after the index event. Diabetes mellitus and a history of stroke were strongly associated with poorer cognitive function after covariate adjustments; hypertension, smoking, and atrial fibrillation had weaker domain-specific associations. While there were no significant differences in domain impairment among ethnoracial groups, some interethnic differences were found in the effects of risk factors on cognition.

Conclusions: This study confirms the high prevalence of PSCI in diverse populations, highlights common risk factors, in particular diabetes mellitus, and points to ethnoracial differences that warrant attention in the development of prevention strategies.

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Figures

Figure 1
Figure 1. Stacked bar chart showing the percentage of impairment in each domain in each study
Each column does not add up to 100%. Impairment is based on the 6.68th percentile. COAST = Cognitive Outcome After Stroke; EpiUSA = Epidemiologic Study of the Risk of Dementia After Stroke; GRECogVASC = Groupe de Réflexion pour l'evaluation Cognitive Vasculaire Study; K-VCIHS = Korean-Vascular Cognitive Impairment Harmonization Standards Study; SAM = Helsinki Stroke Aging Memory Study; SSS = Sydney Stroke Study; VCI = Vascular Cognitive Impairment. *Studies with missing domain score. **Studies not included in the combined sample.
Figure 2
Figure 2. Forest plots of effect of risk factors on cognitive function in global cognition
These 2-stage meta-analyses were used to examine the degree of variability across studies. For pooled effect sizes (ESs), refer to results from the 1-stage meta-analyses presented in table 5 (for global cognition) and data available from Dryad (appendix T15, doi.org/10.5061/dryad.m517990, for results in the 5 domains). CASPER = Cognition and Affect After Stroke: Prospective Evaluation of Risks; CI = confidence interval; COAST = Cognitive Outcome After Stroke; COGFAST-Nigeria = Cognitive Function After Stroke Nigeria; EpiUSA = Epidemiologic Study of the Risk of Dementia After Stroke; GECOG-VASC = Groupe de Réflexion pour l'evaluation Cognitive Vasculaire Study; K-VCIHS = Korean-Vascular Cognitive Impairment Harmonization Standards Study; NEMESIS = North East Melbourne Stroke Incidence Study; NNI = National Neuroscience Institute Study; PROSPER = Prospective Study of Pravastatin in the Elderly at Risk; SAM = Helsinki Stroke Aging Memory Study; SSS = Sydney Stroke Study; STROKDEM = Study of Factors Influencing Post-Stroke Dementia; VCI = Vascular Cognitive Impairment.

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