| Literature DB >> 25308942 |
Andrew B Bondoc1, Sarah Detombe2, Joy Dunmore-Buyze2, Kelly M Gutpell3, Linshan Liu1, Amanda Kaszuba4, Seongryoung Han4, Rebecca McGirr4, Jennifer Hadway5, Maria Drangova6, Lisa M Hoffman7.
Abstract
The purpose of this study was to measure changes in cardiac function as cardiomyopathy progresses in a mouse model of Duchenne muscular dystrophy using 3-D ECG-gated echocardiography. This study is the first to correlate cardiac volumes acquired using 3-D echocardiography with those acquired using retrospectively gated micro-computed tomography (CT). Both were further compared with standard M-mode echocardiography and histologic analyses. We found that although each modality measures a decrease in cardiac function as disease progresses in mdx/utrn(-/-) mice (n = 5) compared with healthy C57BL/6 mice (n = 8), 3-D echocardiography has higher agreement with gold-standard measurements acquired by gated micro-CT, with little standard deviation between measurements. M-Mode echocardiography measurements, in comparison, exhibit considerably greater variability and user bias. Given the radiation dose associated with micro-CT and the geometric assumptions made in M-mode echocardiography to calculate ventricular volume, we suggest that use of 3-D echocardiography has important advantages that may allow for the measurement of early disease changes that occur before overt cardiomyopathy.Entities:
Keywords: 3-D echocardiography; Dilated cardiomyopathy; Duchenne muscular dystrophy; Gated micro-computed tomography; M-Mode echocardiography; mdx/utrn(–/–) mice
Mesh:
Year: 2014 PMID: 25308942 DOI: 10.1016/j.ultrasmedbio.2014.07.015
Source DB: PubMed Journal: Ultrasound Med Biol ISSN: 0301-5629 Impact factor: 2.998