Dong Han, Wang Zhi-Hao, Zhang Na, Liu Si-Da, Zhao Jian-Jun, Liu Song-Yan
Department of Geriatric Medicine, The First Affiliated Hospital of Jilin University, Changchun, China.
Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, China.
Oncotarget. 2017 May 25;8(65):109752-109761. doi: 10.18632/oncotarget.18211. eCollection 2017 Dec 12.
To study the diagnostic and prognostic role of serum galectin-1 (Gal-1) and -3 (Gal-3) in acute ischemic stroke (AIS) patients.
We enrolled 233 patients with first-ever acute ischemic stroke and 252 healthy controls in this study. The AIS severity was evaluated by National Institutes of Health Stroke Scale (NIHSS) scores. The serum Gal-1 and -3 levels were determined. All patients were followed for 1 years and the functional outcome were evaluated by modified Rankin Scale (mRS) scores.
We found that AIS patients had higher serum Gal-1 and -3 levels than controls. The serum Gal-3 level was closely associated with the AIS severity indicated by NHSS and infarction volume. Serum Gal-3 levels were significantly higher in patients with a poor outcome indicated by mRS scores than those in patients with a good outcome. In contrast, the serum Gal-1 is not associated with the severity and outcome of acute AIS patients. Our in vitro studies show that Gal-3 knockdown with siRNA dramatically increased the culture neuron cell viability and reduced apoptosis under oxygen glucose deprivation treatment. Meanwhile, the pro-inflammatory cytokine expression decreased with the inhibition of Gal-3.
Our finding provides a novel biological marker, serum Gal-3, for monitor of acute AIS patients.
研究血清半乳糖凝集素-1(Gal-1)和-3(Gal-3)在急性缺血性脑卒中(AIS)患者中的诊断及预后作用。
本研究纳入了233例首次发生急性缺血性脑卒中的患者及252例健康对照者。采用美国国立卫生研究院卒中量表(NIHSS)评分评估AIS严重程度。测定血清Gal-1和Gal-3水平。对所有患者进行1年随访,并采用改良Rankin量表(mRS)评分评估功能转归。
我们发现AIS患者血清Gal-1和Gal-3水平高于对照组。血清Gal-3水平与由NHSS及梗死体积所提示的AIS严重程度密切相关。mRS评分提示预后不良的患者血清Gal-3水平显著高于预后良好的患者。相比之下,血清Gal-1与急性AIS患者的严重程度及转归无关。我们的体外研究表明,用小干扰RNA(siRNA)敲低Gal-3可显著提高培养的神经元细胞活力,并在氧糖剥夺处理下减少细胞凋亡。同时,促炎细胞因子表达随Gal-3的抑制而降低。
我们的研究结果为监测急性AIS患者提供了一种新的生物标志物——血清Gal-3。