Extensive White Matter Changes Predict Stroke Recurrence up to 5 Years after a First-Ever Ischemic Stroke

被引:29
|
作者
Melkas, S. [1 ,2 ]
Sibolt, G. [1 ,2 ]
Oksala, N. K. J. [3 ,4 ,5 ]
Putaala, J. [1 ,2 ]
Pohjasvaara, T. [1 ,2 ]
Kaste, M. [1 ,2 ]
Karhunen, P. J. [4 ,5 ]
Erkinjuntti, T. [1 ,2 ]
机构
[1] Univ Helsinki, Dept Neurol Sci, Helsinki, Finland
[2] Univ Helsinki, Cent Hosp, Dept Neurol, Helsinki, Finland
[3] Tampere Univ Hosp, Dept Surg, Div Vasc Surg, Tampere, Finland
[4] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
[5] Tampere Univ Hosp, Ctr Lab, Tampere, Finland
关键词
Recurrent stroke; White matter changes; Vascular risk factors; SMALL-VESSEL DISEASE; CAROTID-ARTERY STENOSIS; VISUAL RATING-SCALES; VASCULAR DEMENTIA; POSTSTROKE COHORT; COGNITIVE DECLINE; FOLLOW-UP; LEUKOARAIOSIS; HYPERINTENSITIES; LADIS;
D O I
10.1159/000341404
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: White matter changes (WMCs), a surrogate for small-vessel disease (SVD), have been shown to be associated with a major negative influence on cognition, mood and functioning in daily life. We aimed to investigate whether severe WMCs are a risk factor for recurrent ischemic stroke in a long-term follow-up. Methods: 320 consecutive patients admitted to hospital with a first-ever ischemic stroke were included in the study and followed up for 12 years using extensive national registers. Patients were aged between 55 and 85 years, with a mean age of 70.8 years. WMCs were rated using MRI and stratified into two grades: absent to moderate WMCs versus severe WMCs. Univariate analysis was performed using binary logistic regression analysis, Kaplan-Meier log rank analysis and life table function. To control for factors such as age, education and cardiovascular risk factors, a multivariate Cox regression proportional hazards analysis was made with forced entry. Results: At least one recurrent stroke, nonfatal or fatal, was diagnosed in 76 (23.8%) patients at 5 years and in 127 (39.7%) patients at 12 years. In univariate analysis, only advancing age was associated with WMCs. The cumulative 5-year recurrence risk was 24.5% [95% confidence interval (95% CI) 23.8-25.2] for patients with absent to moderate WMCs and 39.1% (95% CI 38.1-40.1) for patients with severe WMCs. The cumulative 12-year recurrence risk was 48.1% (95% CI 45.5-50.7) for patients with absent to moderate WMCs and 60.9% (95% CI 56.7-65.1) for patients with severe WMCs. In Cox regression proportional hazards analysis, independent predictors of recurrent stroke at 5 years were severe WMCs [hazard ratio (HR) 1.80, 95% CI 1.11-2.95], atrial fibrillation (HR 1.81, 95% CI 1.09-3.02), hypertension (HR 1.69, 95% CI 1.05-2.71) and peripheral arterial disease (HR 1.89, 95% CI 1.06-3.38). At 12 years, only increasing age remained as an independent predictor (HR 1.04, 95% CI 1.02-1.07). In receiver operating characteristic analysis, the area under the curve for severe WMCs was 0.58 (95% CI 0.51-0.65) for the prediction of stroke recurrence within 5 years. Conclusions: In our well-defined cohort of poststroke patients, the presence of severe WMCs was an indicator of stroke recurrence up to 5 years after a first-ever ischemic stroke. WMCs can be considered as an SVD marker that summarizes the effects of several classical risk factors on the small-vessel brain network and therefore can be used as a score for risk stratification of stroke recurrence. Our findings further underline the poor long-term prognosis of cerebral SVD. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:191 / 198
页数:8
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