Kwon Younghoon, McHugh Stephen, Ghoreshi Kayvon, Lyons Genevieve R, Cho Yeilim, Bilchick Kenneth C, Mazimba Sula, Worrall Bradford B, Akoum Nazem, Chen Lin Y, Soliman Elsayed Z
Department of Medicine, University of Virginia, United States; Department of Medicine, Division of Cardiology, University of Washington, 325 9th Ave., 2CT-69.1, Box 359748, Seattle, WA 98104, United States.
Department of Medicine, Temple University, United States.
J Stroke Cerebrovasc Dis. 2020 Sep;29(9):105086. doi: 10.1016/j.jstrokecerebrovasdis.2020.105086. Epub 2020 Jul 2.
P wave indices represent electrocardiographic marker of left atrial pathology. We hypothesized that P wave would be more abnormal in patients presenting with ischemic stroke than a comparable group without ischemic stroke.
We compared P wave terminal force in V1 (PTFV1) between patients admitted with ischemic stroke (case) and patients followed in cardiology clinic (control) at a single medical center. Using logistic regression models, we tested for an association between abnormal PTFV1 (> 4000 µV ms) and ischemic stroke. We also defined several optimal cut-off values of PTFV1 using a LOESS plot and estimated odds ratio of ischemic stroke when moving from one cut-point level to the next higher-level.
A total of 297 patients (case 147, control 150) were included. PTFV1 was higher in patients with vs. those without ischemic stroke (median 4620 vs 3994 µV ms; p=0.006). PTFV1 was similar between cardioembolic/cryptogenic and other stroke subtypes. In multivariable analyses adjusting for sex, obesity, age, and hypertension, the association between abnormal PTFV1 and ischemic stroke ceased to be significant (OR 1.53 [0.95, 2.50], p=0.083). Increase to the next cutoff level of PTFV1 (900, 2000, 3000, 4000, 5000, and 6000 µV ms) was associated with 18% increase in odds of having ischemic stroke (vs. no ischemic stroke) (OR 1.18 [1.02, 1.36], p=0.026).
Patients presenting with acute ischemic stroke are more likely to have abnormal PTFV1. These findings from a real-world clinical setting support the results of cohort studies that left atrial pathology manifested as abnormal PTFV1 is associated with ischemic stroke.
P波指标代表左心房病变的心电图标志物。我们假设,与无缺血性卒中的对照组相比,缺血性卒中患者的P波异常更为明显。
我们比较了在单一医疗中心因缺血性卒中入院的患者(病例组)和心内科门诊随访的患者(对照组)的V1导联P波终末电势(PTFV1)。使用逻辑回归模型,我们检验了异常PTFV1(>4000 μV·ms)与缺血性卒中之间的关联。我们还使用局部加权散点平滑法(LOESS)图定义了PTFV1的几个最佳临界值,并估计了从一个切点水平到下一个更高水平时缺血性卒中的比值比。
共纳入297例患者(病例组147例,对照组150例)。缺血性卒中患者的PTFV1高于无缺血性卒中患者(中位数分别为4620和3994 μV·ms;p=0.006)。心源性/隐源性卒中与其他卒中亚型的PTFV1相似。在对性别、肥胖、年龄和高血压进行校正的多变量分析中,异常PTFV1与缺血性卒中之间的关联不再显著(比值比1.53[0.95,2.50],p=0.083)。PTFV1增加到下一个临界水平(900、2000、3000、4000、5000和6000 μV·ms)与缺血性卒中(与无缺血性卒中相比)的比值增加18%相关(比值比1.18[1.02,1.36],p=0.026)。
急性缺血性卒中患者更有可能出现异常PTFV1。来自真实临床环境的这些发现支持了队列研究的结果,即表现为异常PTFV1的左心房病变与缺血性卒中相关。