P-wave Morphology and Ischemic Stroke
Emerging data already suggests that left atrial disease may be a cause of ischemic stroke in the absence of AF and may be a cause for many strokes classified as cryptogenic. The objective of the study was to examine the association between P-wave morphology and stroke while accounting for incident atrial fibrillation (AF).
The study titled the Multi-Ethnic Study of Atherosclerosis (MESA) enrolled 6814 men and women between the ages of 45 to 84 years. The participants were free from any apparent cerebrovascular or cardiovascular disease, including AF. Incident AF was accounted for during the study as were age, sex, race, hypertension, left ventricular hypertrophy, cholesterol level, lipoprotein levels, diabetes, chronic obstructive pulmonary disease, chronic kidney disease, body mass index and smoking status.
Study researchers obtained 12-lead ECG from each patient's first and last study visit. Each patient's P-wave areas, amplitudes and durations were measured. The authors of the study defined P-wave terminal force in lead V1 (PTFV1) as the duration (in ms) of the downward deflection of the P wave in lead V1 multiplied by the absolute value of its amplitude.
Study participants were followed for a median of 8.5 years. During this time frame, ischemic stroke occurred in 121 patients. PTFV1 was found to be more strongly associated with incident stroke than with incident AF. Association between PTFV1 and stroke was similar for incident AF.
During the study period, it was observed that the association between PTFV1 and subsequent ischemic stroke persisted in participants even without any AF. The findings thus suggest that atrial disease may cause stroke even without the presence of AF. The findings also help explain cryptogenic strokes.
The authors of the study conclude that "P-wave area and terminal force are associated with stroke risk, but did not control for AF, which may mediate the relationship between P-wave morphology and stroke."
Further research is still required to fully understand this association. The authors of the study indicate that they may have missed subclinical AF that could have mediated the association between PTFV1 and stroke. The researchers were also unable to examine the association with embolic-appearing or cryptogenic stroke as well as assess the interaction between ethnicity and P-wave morphology with the risk of stroke. No imaging of the left atrium was performed during this study but the researchers do point out that P-wave measurements are not necessarily captured by imaging data.
However, work still needs to be done to fully delineate the ECG, imaging and biomarker characteristics of atrial cardiopathy. AF may be an imperfect marker of risk and a study of a combination of markers may help understand the risk of left atrial embolization better.
Image credit: Wikimedia Commons
Published on : Mon, 4 Aug 2014
Print as PDF
Always in sight, always in mind Features Mindray believes the best way to predict the future is to create it. The revolutionary BeneVision N22/N19 is designed to optimize user experience by satisfying all your clinical demands. With visionary-stimulating...
Get an complete overview of your POCT setup - from one dashboard Your point-of-care-testing setup probably involves many different types of devices from various manufacturers. Radiometer's AQURE point-of-care management system can give you an overview...
XENIOS AG is a medical device company with the three brands, novalung, i-cor and medos, that run on a single XENIOS platform. This platform enables next-generation therapies for lung and heart failure. No other company except XENIOS AG is offering lung...
Medos customized tubing sets have been individually designed, so that all customer requirements, depending on application and need can be realized. Furthermore tubing sets can be refined by rheoparin or x.eed coating.
The technical and clinical reference standard for all B·R·A·H·M·S PCT assays. All clinical cut-offs and algorithms were developed based on B·R·A·H·M·S PCT sensitive KRYPTOR. Homogeneous immunoassay for the quantitative d