Key result
TRAFF2 and TRAFF3 relaxation times were more sensitive than T1rho to hypertrophic cardiomyopathy-related tissue changes and highly correlated with histologically verified fibrosis in a mouse model.
Why the study?
Can magnetic resonance rotating frame relaxation times (T1ρ, TRAFF2, TRAFF3) detect and follow up myocardial fibrosis in a mouse model of progressive hypertrophic cardiomyopathy?
Can magnetic resonance rotating frame relaxation times (T1ρ, TRAFF2, TRAFF3) detect and follow up myocardial fibrosis in a mouse model of progressive hypertrophic cardiomyopathy?
TRAFF2 and TRAFF3 are sensitive non-invasive MRI markers for detecting and following up myocardial fibrosis in progressive hypertrophic cardiomyopathy without the need for contrast agents.
May enable non-contrast fibrosis imaging in chronic MI models; leaves open human validation for hypertrophic cardiomyopathy monitoring.
Magnetic resonance rotating frame relaxation times are an alternative non‐contrast agent choice for the diagnosis of chronic myocardial infarct. Fibrosis typically occurs in progressive hypertrophic cardiomyopathy. Fibrosis has been imaged in myocardial infarcted tissue using rotating frame relaxation times, which provides the possibility to follow up progressive cardiomyopathy without contrast agents. Mild and severe left ventricular hypertrophy were induced in mice by transverse aortic constriction, and the longitudinal rotating frame relaxation times ( T 1ρ ) and relaxation along the fictitious field ( T RAFF2 , T RAFF3 ) were measured at 5, 10, 24, 62 and 89 days after transverse aortic constriction in vivo . Myocardial fibrosis was verified using Masson's trichrome staining. Increases in the relative relaxation time differences of T 1ρ , together with T RAFF2 and T RAFF3 , between fibrotic and remote tissues over time were observed. Furthermore, T RAFF2 and T RAFF3 showed higher relaxation times overall in fibrotic tissue than T 1ρ . Relaxation time differences were highly correlated with an excess of histologically verified fibrosis. We found that T RAFF2 and T RAFF3 are more sensitive than T 1ρ to hypertrophic cardiomyopathy‐related tissue changes and can serve as non‐invasive diagnostic magnetic resonance imaging markers to follow up the mouse model of progressive hypertrophic cardiomyopathy.
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Khan et al. (2017) studied Progressive hypertrophic cardiomyopathy. Magnetic resonance rotating frame relaxation times (TRAFF2, TRAFF3) vs. T1rho was evaluated on Correlation of relaxation time differences with histologically verified fibrosis. TRAFF2 and TRAFF3 relaxation times were more sensitive than T1rho to hypertrophic cardiomyopathy-related tissue changes and highly correlated with histologically verified fibrosis in a mouse model.
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