Garnier Lucie, Duloquin Gauthier, Meloux Alexandre, Benali Karim, Sagnard Audrey, Graber Mathilde, Dogon Geoffrey, Didier Romain, Pommier Thibaut, Vergely Catherine, Béjot Yannick, Guenancia Charles
Department of Neurology, University Hospital, Dijon, France.
Pathophysiology and Epidemiology of Cerebro-Cardiovascular Diseases (EA 7460), Faculty of Health Sciences, Université de Bourgogne, Université de Bourgogne Franche-Comté, Dijon, France.
Front Cardiovasc Med. 2022 Jul 13;9:949213. doi: 10.3389/fcvm.2022.949213. eCollection 2022.
Intensive screening for atrial fibrillation (AF) has led to a better recognition of this cause in stroke patients. However, it is currently debated whether AF Detected After Stroke (AFDAS) has the same pathophysiology and embolic risk as prior-to-stroke AF. We thus aimed to systematically approach AFDAS using a multimodal approach combining clinical, imaging, biological and electrocardiographic markers.
Patients without previously known AF admitted to the Dijon University Hospital (France) stroke unit for acute ischemic stroke were prospectively enrolled. The primary endpoint was the presence of AFDAS at 6 months, diagnosed through admission ECG, continuous electrocardiographic monitoring, long-term external Holter during the hospital stay, or implantable cardiac monitor if clinically indicated after discharge.
Of the 240 included patients, 77 (32%) developed AFDAS. Compared with sinus rhythm patients, those developing AFDAS were older, more often women and less often active smokers. AFDAS patients had higher blood levels of NT-proBNP, osteoprotegerin, galectin-3, GDF-15 and ST2, as well as increased left atrial indexed volume and lower left ventricular ejection fraction. After multivariable analysis, galectin-3 ≧ 9 ng/ml [OR 3.10; 95% CI (1.03-9.254), = 0.042], NT-proBNP ≧ 290 pg/ml [OR 3.950; 95% CI (1.754-8.892, = 0.001], OPG ≥ 887 pg/ml [OR 2.338; 95% CI (1.015-5.620), = 0.046) and LAVI ≥ 33.5 ml/m [OR 2.982; 95% CI (1.342-6.625), = 0.007] were independently associated with AFDAS.
A multimodal approach combining imaging, electrocardiography and original biological markers resulted in good predictive models for AFDAS. These results also suggest that AFDAS is probably related to an underlying atrial cardiopathy.
[www.ClinicalTrials.gov], identifier [NCT03570060].
对房颤(AF)进行强化筛查已使中风患者对这一病因有了更好的认识。然而,目前对于中风后检测到的房颤(AFDAS)是否与中风前房颤具有相同的病理生理学和栓塞风险仍存在争议。因此,我们旨在采用一种多模式方法,结合临床、影像学、生物学和心电图标志物,系统地研究AFDAS。
前瞻性纳入法国第戎大学医院中风单元收治的既往无房颤病史的急性缺血性中风患者。主要终点是6个月时AFDAS的存在情况,通过入院心电图、连续心电图监测、住院期间长期体外动态心电图监测或出院后根据临床指征使用植入式心脏监测器进行诊断。
在纳入的240例患者中,77例(32%)发生了AFDAS。与窦性心律患者相比,发生AFDAS的患者年龄更大,女性更多,经常吸烟者更少。AFDAS患者的NT-proBNP、骨保护素、半乳糖凝集素-3、生长分化因子-15和ST2血液水平更高,左心房指数容积增加,左心室射血分数降低。多变量分析后,半乳糖凝集素-3≧9 ng/ml [比值比(OR)3.10;95%置信区间(CI)(1.03 - 9.254),P = 0.042]、NT-proBNP≧290 pg/ml [OR 3.950;95% CI(1.754 - 8.892),P = 0.001]、骨保护素≥887 pg/ml [OR 2.338;95% CI(1.015 - 5.620),P = 0.046]和左心房容积指数(LAVI)≥33.5 ml/m² [OR 2.982;95% CI(1.342 - 6.625),P = 0.007]与AFDAS独立相关。
结合影像学、心电图和原始生物学标志物的多模式方法为AFDAS建立了良好的预测模型。这些结果还表明,AFDAS可能与潜在的心房心肌病有关。