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Diastolic wall motion abnormality after myocardial infarction: relation to neurohormonal activation and prognostic
Mirza Husic1, Betina Nørager, Kenneth Egstrup
1Department of Medicine, Svendborg Hospital, Svenborg, Denmark.
Insights
Diastolic wall motion abnormality (WMA) after acute myocardial infarction (AMI) is common and detectable early. This diastolic WMA predicts adverse outcomes and is linked to neurohormonal activation.
Area of Science:
- Cardiology
- Echocardiography
- Myocardial Infarction
Background:
- Systolic wall motion abnormality (WMA) is a known outcome predictor post-acute myocardial infarction (AMI).
- The role and detection of diastolic WMA after AMI were previously unknown.
- This study investigated diastolic WMA using color kinesis.
Purpose of the Study:
- To detect diastolic WMA early after AMI using color kinesis.
- To assess the relationship between diastolic WMA and neurohormonal activation.
- To evaluate the prognostic significance of diastolic WMA in patients with first AMI.
Main Methods:
- 149 patients with first AMI underwent color kinesis and echocardiography within 24 hours.
- N-terminal pro-brain natriuretic peptide levels were measured 3 days post-AMI.
- The study endpoint was cardiac death or heart failure readmission.
Main Results:
- Diastolic WMA exceeded systolic WMA in 97% of patients.
- Diastolic WMA correlated significantly with brain natriuretic peptide and coronary artery disease severity.
- Diastolic WMA independently predicted cardiac death or heart failure readmission.
Conclusions:
- Color kinesis effectively assesses diastolic WMA early after AMI.
- Diastolic WMA is linked to neurohormonal activation and coronary artery disease severity.
- Diastolic WMA provides independent prognostic information in AMI patients.
Background:
Systolic wall motion abnormality (WMA) after acute myocardial infarction (AMI) is a major determinant of outcome; the presence and importance of diastolic WMA after AMI are unknown. We therefore sought to detect diastolic WMA using color kinesis and to assess its relation to neurohormonal activation and its prognostic importance in a consecutive population with a first AMI.
Methods:
Complete color-encoded color kinesis and 2-dimensional and Doppler echocardiography were performed in 149 consecutive patients with documented first AMI within 24 hours of their admission. N-terminal pro-brain natriuretic peptide was measured 3 days after AMI. Study end point was cardiac death or readmission for heart failure.
Results:
Diastolic area of WMA exceeded the systolic area in all but 5 patients (97%) and was significantly correlated with brain natriuretic peptide (unadjusted beta = .67, P < .0001; adjusted for systolic function, age, Killip class, and overall diastolic function beta = .27, P = .007). Diastolic WMA was also correlated with the number of diseased vessels on coronary angiography (beta = .59, P < .0001). During follow-up, 25 patients died and 11 were readmitted because of recurrent heart failure. On univariate analysis, the area of diastolic WMA was a predictor of the composite end point (hazard ratio 1.07 [95% CI 1.05-1.09], P < .0001) and remained a predictor on multivariate Cox analysis after adjustment of well-known risk factors, left ventricular systolic and overall diastolic functions (hazard ratio 1.09 [95% CI 1.06-1.15], P < .001).
Conclusion:
The extent of diastolic WMA can be assessed early after AMI using color kinesis. Diastolic WMA is associated with neurohormonal activation and angiographic severity of coronary artery disease and provides independent prognostic information.
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