Brenière Céline, Méloux Alexandre, Pédard Martin, Marie Christine, Thouant Pierre, Vergely Catherine, Béjot Yannick
Equipe d'Accueil (EA 7460): Physiopathologie et Epidémiologie Cérébro-Cardiovasculaires (PEC2), University Bourgogne Franche-Comté, UFR Sciences de Santé, Dijon, France.
Department of Neurology, University Hospital of Dijon, Dijon, France.
Front Neurol. 2019 Jun 14;10:611. doi: 10.3389/fneur.2019.00611. eCollection 2019.
Growth differentiation factor-15 (GDF-15) has been identified as a robust marker of developing cardiovascular disease, however, little is currently known about its prognostic value in stroke patients. In a context of growing interest to discover new biomarkers in stroke, we aimed to assess the association between circulating GDF-15 levels and three-month mortality in ischemic stroke patients treated with acute revascularization therapy. 173 patients hospitalized for acute ischemic stroke and treated with either intravenous thrombolysis ( = 99, 57.2%), mechanical thrombectomy ( = 41, 23.4%) or combined therapy ( = 33, 19.1%) were prospectively included. Baseline clinical and biological characteristics were recorded. Plasma GDF-15 levels were measured at admission (D0), and at 24 h, 3 and 7 days. Clinical severity was assessed with the National Institutes of Health Stroke Scale (NIHSS) score, and vital status was obtained 3 months after the stroke. At 3 months post-stroke, 32 patients (18.5%) had died. The deceased patients had higher D0 plasma GDF-15 levels (median [IQR]: 2,777 [1,769-5,446] vs. 1,460 [965-2,079] pg/mL, < 0.001). In multivariable logistic regression analysis, D0 GDF-15 levels in the third tertile of the distribution were independently associated with mortality at 3 months (OR = 3.71; 95% CI: 1.09-12.6, = 0.036), even after adjustment for confounding variables including clinical severity. Our data show for the first time that GDF-15 plasma concentration at admission is independently associated with 3-month mortality in ischemic stroke patients treated with acute revascularization therapy. The pathophysiological mechanisms that could explain this association warrant further study.
生长分化因子-15(GDF-15)已被确认为心血管疾病发展的一个有力标志物,然而,目前对于其在中风患者中的预后价值知之甚少。在人们对发现中风新生物标志物的兴趣日益浓厚的背景下,我们旨在评估接受急性血管再通治疗的缺血性中风患者循环GDF-15水平与三个月死亡率之间的关联。前瞻性纳入了173例因急性缺血性中风住院并接受静脉溶栓治疗(n = 99,57.2%)、机械取栓治疗(n = 41,23.4%)或联合治疗(n = 33,19.1%)的患者。记录基线临床和生物学特征。在入院时(D0)、24小时、3天和7天测量血浆GDF-15水平。用美国国立卫生研究院卒中量表(NIHSS)评分评估临床严重程度,并在中风后3个月获得生命状态。中风后3个月时,32例患者(18.5%)死亡。死亡患者入院时血浆GDF-15水平较高(中位数[四分位间距]:2777[1769 - 5446] vs. 1460[965 - 2079] pg/mL,P < 0.001)。在多变量逻辑回归分析中,即使在调整包括临床严重程度在内的混杂变量后,处于分布第三分位数的入院时GDF-15水平与3个月时的死亡率独立相关(比值比 = 3.71;95%置信区间:1.09 - 12.6,P = 0.036)。我们的数据首次表明,接受急性血管再通治疗的缺血性中风患者入院时的血浆GDF-15浓度与3个月死亡率独立相关。可能解释这种关联的病理生理机制值得进一步研究。