TY - JOUR
T1 - Layer-specific strain analysis
T2 - Investigation of regional deformations in a rat model of acute versus chronic myocardial infarction
AU - Bachner-Hinenzon, Noa
AU - Ertracht, Offir
AU - Malka, Assaf
AU - Leitman, Marina
AU - Vered, Zvi
AU - Binah, Ofer
AU - Adam, Dan
PY - 2012/9/1
Y1 - 2012/9/1
N2 - Myocardial infarction (MI) injury extends from the endocardium toward the epicardium. This phenomenon should be taken into consideration in the detection of MI. To study the extent of damage at different stages of MI, we hypothesized that measurement of layer-specific strain will allow better delineation of the MI extent than total wall thickness strain at acute stages but not at chronic stages, when fibrosis and remodeling have already occurred. After baseline echocardiography scans had been obtained, 24 rats underwent occlusion of the left anterior descending coronary artery for 30 min followed by reperfusion. Thirteen rats were rescanned at 24 h post-MI and eleven rats at 2 wk post-MI. Next, rats were euthanized, and histological analysis for MI size was performed. Echocardiographic scans were postprocessed by a layer-specific speckle tracking program to measure the peak circumferential strain (S peak C) at the endocardium, midlayer, and epicardium as well as total wall thickness S peak C. Linear regression for MI size versus S peak C showed that the slope was steeper for the endocardium compared with the other layers (P <0.001), meaning that the endocardium was more sensitive to MI size than the other layers. Moreover, receiver operating characteristics analysis yielded better sensitivity and specificity in the detection of MI using endocardial S peak C instead of total wall thickness S peak C at 24 h post-MI (P <0.05) but not 2 wk later. In conclusion, at acute stages of MI, before collagen deposition, scar tissue formation, and remodeling have occurred, damage may be nontransmural, and thus the use of endocardial S peak C is advantageous over total wall thickness SC peak.
AB - Myocardial infarction (MI) injury extends from the endocardium toward the epicardium. This phenomenon should be taken into consideration in the detection of MI. To study the extent of damage at different stages of MI, we hypothesized that measurement of layer-specific strain will allow better delineation of the MI extent than total wall thickness strain at acute stages but not at chronic stages, when fibrosis and remodeling have already occurred. After baseline echocardiography scans had been obtained, 24 rats underwent occlusion of the left anterior descending coronary artery for 30 min followed by reperfusion. Thirteen rats were rescanned at 24 h post-MI and eleven rats at 2 wk post-MI. Next, rats were euthanized, and histological analysis for MI size was performed. Echocardiographic scans were postprocessed by a layer-specific speckle tracking program to measure the peak circumferential strain (S peak C) at the endocardium, midlayer, and epicardium as well as total wall thickness S peak C. Linear regression for MI size versus S peak C showed that the slope was steeper for the endocardium compared with the other layers (P <0.001), meaning that the endocardium was more sensitive to MI size than the other layers. Moreover, receiver operating characteristics analysis yielded better sensitivity and specificity in the detection of MI using endocardial S peak C instead of total wall thickness S peak C at 24 h post-MI (P <0.05) but not 2 wk later. In conclusion, at acute stages of MI, before collagen deposition, scar tissue formation, and remodeling have occurred, damage may be nontransmural, and thus the use of endocardial S peak C is advantageous over total wall thickness SC peak.
KW - Left ventricular function
KW - Myocardial viability
KW - Speckle tracking
KW - Transmurality
UR - http://www.scopus.com/inward/record.url?scp=84865736294&partnerID=8YFLogxK
U2 - 10.1152/ajpheart.00294.2012
DO - 10.1152/ajpheart.00294.2012
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AN - SCOPUS:84865736294
SN - 0363-6135
VL - 303
SP - H549-H558
JO - American Journal of Physiology - Heart and Circulatory Physiology
JF - American Journal of Physiology - Heart and Circulatory Physiology
IS - 5
ER -