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Article Abstract
Background: DNA damage in cardiomyocytes is a key pathological pathway in heart failure progression. It is a reversible process that precedes apoptosis and fibrosis. However, the utility of cardiovascular magnetic resonance T mapping for assessing DNA damage is uncertain.
Objectives: This study aimed to evaluate the relationship between T mapping and cardiomyocyte DNA damage in patients with dilated cardiomyopathy (DCM).
Methods: We identified 36 recent-onset DCM patients undergoing endomyocardial biopsy and serial 3T cardiovascular magnetic resonance before and after guideline-directed therapy. Extracellular volume (ECV) was quantified from native and postcontrast T mapping. DNA damage was assessed via poly(ADP-ribose) quantification in biopsy specimens, alongside collagen volume fraction (CVF) measurement.
Results: Native T and ECV showed a strong correlation with histological CVF (r = 0.62 and r = 0.67, respectively; P < 0.001), while native T moderately correlated with the severity of cardiomyocyte DNA damage (r = 0.41, P = 0.01), but ECV did not. This association remained significant after controlling for CVF. Patients with substantial DNA damage have significantly higher native T for an equivalent ECV (P = 0.004). In the absence of severe fibrosis, myocardial tissue recovery following guideline-directed therapy, along with improvements in left ventricular ejection fraction and reductions in left ventricular cavities, was associated with baseline DNA damage (r = -0.49, P = 0.004) but not with CVF (r = -0.17, P = 0.38).
Conclusions: Native T mapping effectively detects DNA damage and fibrosis, revealing different pathophysiological mechanisms behind the increased native T and ECV. A disproportionate increase in native T relative to ECV suggests early myocardial injury preceding fibrosis in DCM, with potential implications for myocardial tissue recovery after guideline-directed therapy.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12311530 | PMC |
| http://dx.doi.org/10.1016/j.jacadv.2025.102013 | DOI Listing |
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