1. INFORMANT-REPORTED DECLINE ASSOCIATES WITH SILENT ACUTE STROKE LESIONS ANDWORSE SMALL VESSEL DISEASE IN MILD STROKE PATIENTS.
- Author
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Clancy, U., Garcia, D. J., Hewins, W., Stringer, M., Thrippleton, M., Chappell, F. M., Brown, R., Blair, G., Arteaga, C., Valdes-Hernadez, M., Wiseman, S., Hamilton, I., Job, D., Doubal, F. N., and Wardlaw, J. M.
- Subjects
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DIAGNOSIS of dementia , *COGNITION disorders , *CONFERENCES & conventions , *STROKE patients , *LIFE skills , *EARLY diagnosis - Abstract
Introduction: Small vessel disease (SVD) commonly causes stroke and dementia. Early clinical predictors of disease progression are lacking. We aimed to determine whether informant reports of chronic cognitive/functional decline, prerequisites for dementia diagnosis, are associated with (a)baseline SVD burden, measured by Fazekas scores and (b)SVD change, measured by incident subcortical Diffusion-weighted Imaging (DWI) lesions. Method: We prospectively recruited patients with mild ischaemic stroke, performed diagnostic MRI, and invited participants to repeat MRI 3- to 6-monthly. Informants completed the Informant Questionnaire for Cognitive Decline in the Elderly (IQCODE) prior to baseline visit, a 16-item questionnaire which assesses patients’ cognitive and functional decline in the preceding ten years. Scores range from 1–5: a score above 3.3 has high sensitivity/specificity for dementia post-stroke. We conducted linear regression with IQCODE as the dependent variable, adjusting for age, sex, baseline MoCA, disability (modified Rankin Scale). Results: We recruited 106 participants (mean age 67 years;range 40–86;33% female). Ninety-three informant questionnaires were returned. IQCODE associated with baseline Fazekas score; Fazekas 6 (β =0.28, p=0.04) vs. Fazekas 3 (β =0.03, p=0.67), R2=0.11, adjusted for age, sex, baseline MoCA, disability. IncidentDWI lesions were common (15/106; 14/15 subcortical; no active embolic sources; median 67 days post-stroke). Four were asymptomatic, two reported stroke-like symptoms and nine had neuropsychiatric/non-focal symptoms. IQCODE was higher in those with a new lesion vs. without (β =0.21, p=0.02), R2=0.09, while age (β =−0.004, p=0.19), MoCA (β =−0.006, p=0.56) and disability (β =0.06, p=0.2) were not. Conclusions: Higher SVD burden and incident, mostly “silent” stroke lesions associate more strongly with informant concerns of cognitive/functional decline than age or objective cognitive tests. These findings are novel in an ischaemic stroke population and the first to assess IQCODE/SVD progression. Future work should determine whether combining informant reports with imaging features of small vessel disease improves early detection of dementia. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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