Turaj W, Słowik A, Wyrwicz-Petkow U, Pankiewicz J, Iskra T, Rudzińska M, Szczudlik A
Department of Neurology, Collegium Medicum, Jagiellonian University, Cracow, Poland.
Med Sci Monit. 2001 Sep-Oct;7(5):989-94.
Microalbuminuria (MA) is thought to be a marker of widespread vascular damage. It is associated with increased mortality in diabetes mellitus, hypertension and acute myocardial infarction. The aim of the present study was to evaluate the prognostic significance of MA in non-diabetic acute stroke patients.
We studied 52 patients (mean age 69.3 +/- 12.5 years) diagnosed with ischemic stroke confirmed by computed tomography, who were admitted to the Stroke Unit within 24 hours after the onset of symptoms. The control group consisted of 37 age- and gender-matched subjects (mean age 65.2 +/- 5.7 years), examined 3 to 18 months after ischemic stroke. We excluded patients with diabetes mellitus, positive urinalysis, proteinuria, hepatic or renal insufficiency, neoplastic disease or clinical signs of infection. The severity of the neurological deficit was assessed by the Scandinavian Stroke Scale (SSS). The albumin excretion rate was measured in daily urine collection on the second day of hospitalization, using the immunonephelometric method. The patients were followed up for three months.
MA was found in 24 of 52 (46.1%) acute stroke patients and in 5 of 37 (13.5%) controls (p<0.05). Patients with MA scored lower on the SSS than patients without MA, both on admission and later. We found a correlation between the daily excretion of albumin and the severity of neurological deficit on admission, as expressed by the SSS score (r = -0.48, p<0.05). The 90-day mortality rate was higher in patients with MA as compared to patients without MA (45.8% vs 7.1%). Patients with MA scored lower on the Barthel Index on Day 90 (median: 65 vs 100, p<0.01).
We found that MA can be detected in about 46% of non-diabetic patients with acute ischemic stroke. Measuring the albumin excretion rate may be a reliable predictor of increased mortality 3 months after stroke.
微量白蛋白尿(MA)被认为是广泛血管损伤的一个标志物。它与糖尿病、高血压及急性心肌梗死患者死亡率增加相关。本研究的目的是评估MA在非糖尿病急性卒中患者中的预后意义。
我们研究了52例经计算机断层扫描确诊为缺血性卒中的患者(平均年龄69.3±12.5岁),这些患者在症状发作后24小时内被收入卒中单元。对照组由37例年龄和性别匹配的受试者组成(平均年龄65.2±5.7岁),在缺血性卒中后3至18个月接受检查。我们排除了患有糖尿病、尿分析阳性、蛋白尿、肝或肾功能不全、肿瘤性疾病或感染临床体征的患者。采用斯堪的纳维亚卒中量表(SSS)评估神经功能缺损的严重程度。在住院第二天,采用免疫比浊法测定每日尿液收集样本中的白蛋白排泄率。对患者进行了三个月的随访。
52例急性卒中患者中有24例(46.1%)发现有MA,37例对照组中有5例(13.5%)发现有MA(p<0.05)。有MA的患者在入院时及之后的SSS评分均低于无MA的患者。我们发现白蛋白每日排泄量与入院时神经功能缺损严重程度之间存在相关性,用SSS评分表示(r = -0.48,p<0.05)。与无MA的患者相比,有MA的患者90天死亡率更高(45.8%对7.1%)。有MA的患者在第90天时Barthel指数评分更低(中位数:65对100,p<0.01)。
我们发现约46%的非糖尿病急性缺血性卒中患者可检测到MA。测量白蛋白排泄率可能是卒中后3个月死亡率增加的可靠预测指标。