Myocardial Effective Transverse Relaxation Time T2* is Elevated in Hypertrophic Cardiomyopathy: A 7.0 T Magnetic Resonance Imaging Study

被引:7
|
作者
Huelnhagen, Till [1 ]
Ku, Min-Chi [1 ,2 ]
Reimann, Henning Matthias [1 ]
Duarte, Teresa Serradas [1 ]
Pohlmann, Andreas [1 ]
Flemming, Bert [3 ]
Seeliger, Erdmann [3 ]
Eichhorn, Christina [4 ]
Ferrari, Victor A. [5 ,6 ]
Prothmann, Marcel [2 ,7 ]
Schulz-Menger, Jeanette [2 ,7 ]
Niendorf, Thoralf [1 ,2 ,8 ]
机构
[1] Helmholtz Assoc, Max Delbruck Ctr Mol Med, BUFF, Berlin, Germany
[2] DZHK German Ctr Cardiovasc Res, Partner Site, Berlin, Germany
[3] Charite, Inst Vegetat Physiol, Berlin, Germany
[4] Helmholtz Assoc, Max Delbruck Ctr Mol Med, Dept Informat Technol, Stat Sci, Berlin, Germany
[5] Univ Penn, Perelman Sch Med, Div Cardiovasc Med, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Penn Cardiovasc Inst, Philadelphia, PA 19104 USA
[7] Expt & Clin Res Ctr, Working Grp Cardiovasc Magnet Resonance, Berlin, Germany
[8] Expt & Clin Res Ctr, Berlin, Germany
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
LATE GADOLINIUM ENHANCEMENT; SUDDEN-DEATH; MICROVASCULAR DYSFUNCTION; PROGNOSTIC VALUE; RISK; ABNORMALITIES; CAPILLARY; THICKNESS; DESIGN; IMAGES;
D O I
10.1038/s41598-018-22439-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the myocardium and bares the risk of progression to heart failure or sudden cardiac death. Identifying patients at risk remains an unmet need. Recognizing the dependence of microscopic susceptibility on tissue microstructure and on cardiac macromorphology we hypothesized that myocardial T-2* might be altered in HCM patients compared to healthy controls. To test this hypothesis, myocardial T-2*-mapping was conducted at 7.0 Tesla to enhance T-2*-contrast. 2D CINE T-2*-mapping was performed in healthy controls and HCM patients. To ensure that T-2* is not dominated by macroscopic magnetic field inhomogeneities, volume selective B-0 shimming was applied. T-2* changes in the interventricular septum across the cardiac cycle were analyzed together with left ventricular radius and ventricular septal wall thickness. The results show that myocardial T-2* is elevated throughout the cardiac cycle in HCM patients compared to healthy controls. A mean septal T-2* = 13.7 +/- 1.1 ms (end-systole: T-2*,(systole) = 15.0 +/- 2.1, end-diastole: T-2*,(diastole) = 13.4 +/- 1.3 ms, T-2*,(systole)/T-2*,(diastole) ratio = 1.12) was observed in healthy controls. For HCM patients a mean septal T-2* = 17.4 +/- 1.4 ms (end-systole: T-2*,(systole) = 17.7 +/- 1.2 ms, end-diastole: T-2*,(diastole) = 16.2 +/- 2.5 ms, T-2*,T-systole/(2)*,(diastole) ratio = 1.09) was found. Our preliminary results provide encouragement that assessment of T-2* and its changes across the cardiac cycle may benefit myocardial tissue characterization in HCM.
引用
收藏
页数:9
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