Progression of diffuse myocardial fibrosis assessed by cardiac magnetic resonance T^sub 1^ mapping

To evaluate long-term changes in diffuse myocardial fibrosis using cardiac magnetic resonance (CMR) with late gadolinium enhancement (LGE) and T^sub 1^ mapping. Patients with chronic stable cardiomyopathy and stable clinical status (n = 52) underwent repeat CMR at a 6 month or greater follow up inte...

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Veröffentlicht in:The international journal of cardiovascular imaging 2014-10, Vol.30 (7), p.1339
Hauptverfasser: Yi, Colin J, Yang, Eunice, Lai, Shenghan, Gai, Neville, Liu, Chia, Liu, Songtao, Zimmerman, Stefan L, Lima, João A, C, Bluemke, David A
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Sprache:eng
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Zusammenfassung:To evaluate long-term changes in diffuse myocardial fibrosis using cardiac magnetic resonance (CMR) with late gadolinium enhancement (LGE) and T^sub 1^ mapping. Patients with chronic stable cardiomyopathy and stable clinical status (n = 52) underwent repeat CMR at a 6 month or greater follow up interval and had LGE and left ventricular (LV) T^sub 1^ mapping CMR. Diffuse myocardial fibrosis (excluding areas of focal myocardial scar) was assessed by post gadolinium myocardial T^sub 1^ times. Mean baseline age of 52 patients (66 % male) was 35 ± 19 years with a mean interval between CMR examinations of 2.0 ± 0.8 years. CMR parameters, including LV mass and ejection fraction, showed no change at follow-up CMR (p > 0.05). LVT^sub 1^ times (excluding focal scar) decreased over the study interval (from 468 ± 106 to 434 ± 82 ms, p = 0.049). 38 Patients had no visual LGE-, while 14 were LGE+. For LGE- patients, greater change in LV mass and end systolic volume index were associated with change in T^sub 1^ time ([beta] = -2.03 ms/g/m^sup 2^, p = 0.035 and [beta] = 2.1 ms/mL/m^sup 2^, p = 0.029, respectively). For LGE+ patients, scar size was stable between CMR1 and CMR2 (10.7 ± 13.8 and 11.5 ± 13.9 g, respectively, p = 0.32). These results suggest that diffuse myocardial fibrosis, as assessed by T^sub 1^ mapping, progresses over time in patients with chronic stable cardiomyopathy.[PUBLICATION ABSTRACT]
ISSN:1569-5794
1573-0743
DOI:10.1007/s10554-014-0459-z