Suppr超能文献

基于 MRI 的小鼠心肌梗死后心脏不良重构预测。

MRI-based prediction of adverse cardiac remodeling after murine myocardial infarction.

机构信息

Cardiovascular Division, King's College London British Heart Foundation Centre of Excellence, United Kingdom.

出版信息

Am J Physiol Heart Circ Physiol. 2012 Aug 1;303(3):H309-14. doi: 10.1152/ajpheart.00208.2012. Epub 2012 May 25.

Abstract

Myocardial infarction (MI) results in adverse cardiac remodeling leading to heart failure and increased mortality. Experimental mouse models of MI are extensively used to identify mechanisms underlying adverse remodeling, but the extent of remodeling that occurs may be highly variable and can limit the utility to discover new disease pathways. The ability to predict the development of significant late post-MI remodeling would be invaluable in conducting such studies by increasing throughput and efficiency. This study aimed to identify potential thresholds of cardiac magnetic resonance imaging (MRI) parameters measured early after murine MI that would predict the development of significant adverse remodeling at 4 wk. MI was achieved by permanent coronary ligation and animals (n = 84) were followed up for 4 wk subsequently. MRI was used to assess left ventricular (LV) volumes, mass and ejection fraction, as well as infarct size (IS). Late gadolinium enhancement cine-MRI was performed at 2 days with standard cine-MRI at 30 days post-MI. Utilizing multiple logistic regression, we found that IS >36%, at 2 days post-MI, was the overall best single predictor of adverse remodeling at 30 days (sensitivity 80.7%, specificity 88.9%; C-statistic of 0.939 from receiver-operating curve analysis). LV end-systolic volume (LVESV) >32 μl was also an excellent predictor comparable to IS. The combination of IS >36% and/or LVESV >32 μl provided the highest predictive values for late adverse remodeling among multiple predictors. This study demonstrates that MRI-based estimation of IS and ESV during the acute phase of murine MI are good predictors of subsequent adverse remodeling that may aid experimental design.

摘要

心肌梗死(MI)导致不良心脏重构,导致心力衰竭和死亡率增加。MI 的实验小鼠模型被广泛用于确定不良重构的潜在机制,但发生的重构程度可能高度可变,并且可能限制发现新疾病途径的效用。能够预测 MI 后晚期发生显著重构的能力对于进行此类研究非常有价值,因为它可以提高通量和效率。本研究旨在确定 MI 后早期测量的心脏磁共振成像(MRI)参数的潜在阈值,这些参数可以预测 4 周时发生显著不良重构的可能性。通过永久性冠状动脉结扎实现 MI,随后对动物(n = 84)进行了 4 周的随访。使用 MRI 评估左心室(LV)容积、质量和射血分数以及梗死面积(IS)。在 MI 后第 2 天进行晚期钆增强电影 MRI,在第 30 天进行标准电影 MRI。利用多变量逻辑回归,我们发现 MI 后第 2 天 IS >36%是 30 天不良重构的整体最佳单一预测因子(敏感性 80.7%,特异性 88.9%;来自受试者工作特征曲线分析的 C 统计量为 0.939)。LV 收缩末期容积(LVESV)>32 μl 也是与 IS 相当的优秀预测因子。IS >36%和/或 LVESV >32 μl 的组合在多个预测因子中为晚期不良重构提供了最高的预测值。本研究表明,在 MI 的急性阶段基于 MRI 的 IS 和 ESV 估计是随后不良重构的良好预测因子,这可能有助于实验设计。

相似文献

1
MRI-based prediction of adverse cardiac remodeling after murine myocardial infarction.
Am J Physiol Heart Circ Physiol. 2012 Aug 1;303(3):H309-14. doi: 10.1152/ajpheart.00208.2012. Epub 2012 May 25.
2
The impact of infarct size on regional and global left ventricular systolic function: a cardiac magnetic resonance imaging study.
Int J Cardiovasc Imaging. 2015 Jun;31(5):1037-44. doi: 10.1007/s10554-015-0657-3. Epub 2015 Apr 12.
7
Post-Myocardial Infarction Remodeling and Hyperkinetic Remote Myocardium in Sheep Measured by Cardiac MRI Feature Tracking.
J Magn Reson Imaging. 2025 Mar;61(3):1323-1335. doi: 10.1002/jmri.29496. Epub 2024 Jun 28.
8
MRI with gadofosveset: A potential marker for permeability in myocardial infarction.
Atherosclerosis. 2018 Aug;275:400-408. doi: 10.1016/j.atherosclerosis.2018.04.024. Epub 2018 Apr 25.
9
Pathophysiology of LV Remodeling Following STEMI: A Longitudinal Diffusion Tensor CMR Study.
JACC Cardiovasc Imaging. 2023 Feb;16(2):159-171. doi: 10.1016/j.jcmg.2022.04.002. Epub 2022 Jun 15.

引用本文的文献

1
MRI with gadofosveset: A potential marker for permeability in myocardial infarction.
Atherosclerosis. 2018 Aug;275:400-408. doi: 10.1016/j.atherosclerosis.2018.04.024. Epub 2018 Apr 25.
3
Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction.
Int J Cardiol Heart Vasc. 2016 Mar 16;11:29-34. doi: 10.1016/j.ijcha.2016.03.005. eCollection 2016 Jun.
4
Toll-like receptor 9 prevents cardiac rupture after myocardial infarction in mice independently of inflammation.
Am J Physiol Heart Circ Physiol. 2016 Dec 1;311(6):H1485-H1497. doi: 10.1152/ajpheart.00481.2016. Epub 2016 Oct 21.
5
Cell-specific effects of Nox2 on the acute and chronic response to myocardial infarction.
J Mol Cell Cardiol. 2016 Sep;98:11-7. doi: 10.1016/j.yjmcc.2016.07.003. Epub 2016 Jul 7.
9
Dysfunction of the CNS-heart axis in mouse models of Huntington's disease.
PLoS Genet. 2014 Aug 7;10(8):e1004550. doi: 10.1371/journal.pgen.1004550. eCollection 2014 Aug.
10
The role of 1.5 tesla MRI and anesthetic regimen concerning cardiac analysis in mice with cardiomyopathy.
PLoS One. 2014 Apr 18;9(4):e94615. doi: 10.1371/journal.pone.0094615. eCollection 2014.

本文引用的文献

4
Advanced methods for quantification of infarct size in mice using three-dimensional high-field late gadolinium enhancement MRI.
Am J Physiol Heart Circ Physiol. 2009 Apr;296(4):H1200-8. doi: 10.1152/ajpheart.01294.2008. Epub 2009 Feb 13.
7
Involvement of Nox2 NADPH oxidase in adverse cardiac remodeling after myocardial infarction.
Hypertension. 2008 Feb;51(2):319-25. doi: 10.1161/HYPERTENSIONAHA.107.101980. Epub 2008 Jan 7.
8
Effect of left ventricular scar size, location, and transmurality on left ventricular remodeling with healed myocardial infarction.
Am J Cardiol. 2007 Apr 15;99(8):1109-14. doi: 10.1016/j.amjcard.2006.11.059. Epub 2007 Feb 21.
9
Myocardial infarct size measurement in the mouse chronic infarction model: comparison of area- and length-based approaches.
J Appl Physiol (1985). 2007 Jun;102(6):2104-11. doi: 10.1152/japplphysiol.00033.2007. Epub 2007 Mar 8.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验