Onteddu Sanjeeva R, Goddeau Richard P, Minaeian Artin, Henninger Nils
Department of Neurology, University of Massachusetts Medical School, Worcester, MA, United States.
Department of Neurology, University of Massachusetts Medical School, Worcester, MA, United States; Department of Psychiatry, University of Massachusetts Medical School, Worcester, MA, United States.
J Neurol Sci. 2015 Dec 15;359(1-2):418-23. doi: 10.1016/j.jns.2015.10.005. Epub 2015 Oct 8.
Ischemic stroke remains a leading cause of disability, particularly among the elderly, but this association has not been consistently noted among patients with minor stroke. We sought to determine the association of chronological age and leukoaraiosis, which is considered a marker of biological age, with the degree of neurological deficit recovery and 90-day disability after minor ischemic stroke.
We retrospectively analyzed 185 patients with a minor ischemic stroke (National Institutes of Health Stroke Scale [NIHSS] score ≤ 5). Leukoaraiosis severity was graded according to the van Swieten scale. NIHSS was assessed at baseline, discharge, and 90-days. Multivariable linear and ordinal logistic regression analyses were constructed to identify independent predictors of the degree of NIHSS-improvement (ΔNIHSS) and 90-day outcome as assessed by the modified Rankin Scale (mRS).
Patients with severe leukoaraiosis had attenuated ΔNIHSS at 90 days as compared to patients with none-to-mild leukoaraiosis (p=0.028). After adjustment, leukoaraiosis severity (p<0.001) but not chronological age (p=0.771) was independently associated with the ΔNIHSS by day 90. Severe leukoaraiosis (p=0.003, OR 3.1, 95%-CI 1.5-6.4), older age (p=0.001, OR 1.0 95%-CI 1.0-1.1), and admission NIHSS (p<0.001, OR 1.5, 95%-CI 1.2-1.8) were independent predictors of the 90-day mRS.
Leukoaraiosis is a more sensitive predictor for neurological deficit recovery after ischemic stroke than chronological age. Further study is required to establish the specific contribution of leukoaraiosis to functional outcome after minor ischemic stroke beyond its impact on recovery mechanisms.
缺血性卒中仍然是导致残疾的主要原因,在老年人中尤为如此,但在轻度卒中患者中,这种关联并不一致。我们试图确定实际年龄和脑白质疏松症(被认为是生物学年龄的一个标志)与轻度缺血性卒中后神经功能缺损恢复程度和90天残疾情况之间的关联。
我们回顾性分析了185例轻度缺血性卒中患者(美国国立卫生研究院卒中量表[NIHSS]评分≤5)。脑白质疏松症严重程度根据范·斯维滕量表进行分级。在基线、出院时和90天时评估NIHSS。构建多变量线性和有序逻辑回归分析,以确定NIHSS改善程度(ΔNIHSS)和改良Rankin量表(mRS)评估的90天结局的独立预测因素。
与无至轻度脑白质疏松症的患者相比,重度脑白质疏松症患者在90天时的ΔNIHSS有所减弱(p = 0.028)。调整后,脑白质疏松症严重程度(p < 0.001)而非实际年龄(p = 0.771)与90天时的ΔNIHSS独立相关。重度脑白质疏松症(p = 0.003,OR 3.1,95%CI 1.5 - 6.4)、高龄(p = 0.001,OR 1.0 95%CI 1.0 - 1.1)和入院时NIHSS(p < 0.001,OR 1.5,95%CI 1.2 - 1.8)是90天mRS的独立预测因素。
脑白质疏松症比实际年龄对缺血性卒中后神经功能缺损恢复更敏感。需要进一步研究以确定脑白质疏松症对轻度缺血性卒中后功能结局的具体贡献,超出其对恢复机制的影响。