4.6 Article

Quantification of murine myocardial infarct size using 2-D and 4-D high-frequency ultrasound

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00476.2021

关键词

echocardiography; infarct size; mouse models; strain; ultrasound

资金

  1. Diabetes New Investigator Grant
  2. Indiana University Medical Student Program for Research
  3. Indiana Clinical and Translational Sciences Institute - National Institutes of Health, National Center for Advancing Translational Sciences, Clinical and Translational Sciences Award [TL1TR002531, UL1TR002529]

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Ischemic heart disease is a leading cause of death globally and in the United States and Canada. This study demonstrates the effectiveness of using echocardiographic techniques to measure the size of myocardial infarction. Both two-dimensional and four-dimensional echocardiography methods were reliable in assessing the infarct size, with four-dimensional analysis providing a more comprehensive view of left ventricle function and structure. Strain analysis on four-dimensional data also accurately identifies infarct size and regional left ventricular dysfunction. These techniques can enhance our understanding of the impact of pharmacological interventions on cardiac disease.
Ischemic heart disease is the leading cause of death in the United States, Canada, and worldwide. Severe disease is characterized by coronary artery occlusion, loss of blood flow to the myocardium, and necrosis of tissue, with subsequent remodeling of the heart wall, including fibrotic scarring. The current study aims to demonstrate the efficacy of quantitating infarct size via two-dimensional (2-D) echocardiographic akinetic length and four-dimensional (4-D) echocardiographic infarct volume and surface area as in vivo analysis techniques. We further describe and evaluate a new surface area strain analysis technique for estimating myocardial infarction (MI) size after ischemic injury. Experimental MI was induced in mice via left coronary artery ligation. Ejection fraction and infarct size were measured through 2-D and 4-D echocardiography. Infarct size established via histology was compared with ultrasound-based metrics via linear regression analysis. Two-dimensional echocardiographic akinetic length (r = 0.76, P = 0.03), 4-D echocardiographic infarct volume (r = 0.85, P = 0.008), and surface area (r = 0.90, P = 0.002) correlate well with histology. Although both 2-D and 4-D echocardiography were reliable measurement techniques to assess infarct, 4-D analysis is superior in assessing asymmetry of the left ventricle and the infarct. Strain analysis performed on 4-D data also provides additional infarct sizing techniques, which correlate with histology (surface strain: r = 0.94, P < 0.001, transmural thickness: r = 0.76, P = 0.001). Two-dimensional echocardiographic akinetic length, 4-D echocardiography ultrasound, and strain provide effective in vivo methods for measuring fibrotic scarring after MI. NEW & NOTEWORTHY Our study supports that both 2-D and 4-D echocardiographic analysis techniques are reliable in quantifying infarct size though 4-D ultrasound provides a more holistic image of LV function and structure, especially after myocardial infarction. Furthermore, 4-D strain analysis correctly identifies infarct size and regional LV dysfunction after MI. Therefore, these techniques can improve functional insight into the impact of pharmacological interventions on the pathophysiology of cardiac disease.

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