Rainer Timothy H, Wong Lawrence K S, Lam Wynnie, Yuen Eddie, Lam Nicole Y L, Metreweli Constantine, Lo Y M Dennis
Accident and Emergency Medicine Academic Unit, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong Special Administrative Region.
Clin Chem. 2003 Apr;49(4):562-9. doi: 10.1373/49.4.562.
At present there is no simple, accurate blood test that may be used to determine the severity of stroke or to predict mortality and morbidity in stroke patients presenting to emergency departments.
Patients with stroke-like symptoms who presented to an emergency department of a university hospital in Hong Kong were recruited for the study. DNA extracted from patients' plasma was analyzed for the beta-globin gene with a fluorescent-based PCR test. The primary outcome measures were in-hospital and 6-month mortality and morbidity using the post-stroke modified Rankin Score.
Among the 88 consecutive patients recruited to the study, 70 (80%) had ischemic stroke, 11 (13%) had intracerebral hemorrhage, and 7 (8%) had transient ischemic attacks. Median plasma DNA concentrations taken within 3 h of symptom onset were higher in patients who died compared with those who survived at discharge (6205 vs 1334 kilogenome-equivalents/L; P = 0.03). Among patients with NIH Stroke Scale scores >8, median plasma DNA concentrations were higher in patients who died compared with those who survived to 6 months (2273 vs 968 kilogenome-equivalents/L; P = 0.002). Plasma DNA concentrations correlated with the volume of cerebral hematoma (r = 0.66; P = 0.03). Plasma DNA concentrations >1400 kilogenome-equivalents/L had a sensitivity of 100% and a specificity of 74.4% for predicting hospital mortality after stroke, and the area under the ROC curve was 0.89 (95% confidence interval, 0.80-0.94). The adjusted odds ratio for plasma DNA concentrations predicting 6-month mortality was 1.6 (1.1-2.4; P = 0.03) and for predicting 6-month post-Rankin Score >2 was 1.8 (1.0-3.3; P = 0.05).
Plasma DNA concentrations correlate with stroke severity and may be used to predict mortality and morbidity in the emergency room.
目前尚无简单、准确的血液检测方法可用于确定中风的严重程度或预测就诊于急诊科的中风患者的死亡率和发病率。
招募到香港一所大学医院急诊科出现类似中风症状的患者进行研究。采用基于荧光的聚合酶链反应检测分析从患者血浆中提取的DNA的β-珠蛋白基因。主要结局指标是使用中风后改良Rankin量表评估的住院期间及6个月时的死亡率和发病率。
在连续纳入该研究的88例患者中,70例(80%)为缺血性中风,11例(13%)为脑出血,7例(8%)为短暂性脑缺血发作。症状发作后3小时内采集的血浆DNA浓度中位数,死亡患者高于出院存活患者(6205对1334千基因组当量/升;P = 0.03)。在国立卫生研究院中风量表评分>8的患者中,死亡患者的血浆DNA浓度中位数高于存活至6个月的患者(2273对968千基因组当量/升;P = 0.002)。血浆DNA浓度与脑血肿体积相关(r = 0.66;P = 0.03)。血浆DNA浓度>1400千基因组当量/升对预测中风后医院死亡率的敏感度为100%,特异度为74.4%,ROC曲线下面积为0.89(95%置信区间,0.80 - 0.94)。血浆DNA浓度预测6个月死亡率的校正比值比为1.6(1.1 - 2.4;P = 0.03),预测6个月改良Rankin量表评分>2的校正比值比为1.8(1.0 - 3.3;P = 0.05)。
血浆DNA浓度与中风严重程度相关,可用于在急诊室预测死亡率和发病率。