In patients with Duchenne muscular dystrophy, late gadolinium enhancement was present in 36% of subjects and its prevalence was significantly higher in those with reduced left ventricular ejection fraction (OR 12.3).
Observational (n=314)
No
In patients with Duchenne muscular dystrophy, myocardial fibrosis detected by late gadolinium enhancement occurs early, is progressive, and strongly correlates with older age, reduced left ventricular ejection fraction, and mortality.
Effect estimate: OR 12.3 (95% CI 4.9-30.6)
Absolute Event Rate: 84% vs 30%
p-value: p=<0.0001
BACKGROUND: Duchenne muscular dystrophy (DMD), an X-linked disorder affects approximately 1 in 5000 males, is universally associated with heart disease. We previously identified myocardial disease by late gadolinium enhancement (LGE) in DMD subjects at various stages of disease, but the true prevalence is unclear. Cardiovascular magnetic resonance (CMR) is well established for both assessment of ventricular function and myocardial fibrosis by LGE. We sought to establish i) prevalence and distribution of LGE in a large DMD population and ii) relationship among LGE, age, LVEF by CMR and current living status. METHODS: Current living status, demographic and CMR data including ventricular volumes, LVEF and LGE from 314 DMD patients undergoing evaluation at a single large tertiary referral center were analyzed. RESULTS: 113 of 314 (36%) of DMD subjects showed LGE positivity with prevalence increasing from 17% of patients 15 years-old. Patients with LVEF ≥55% were LGE positive in 30% of cases; this increased to 84% for LVEF <55%. LGE was more prevalent in the free wall (531/1243, 42.7%) vs. septal segments (30/565, 5.3%). Patients with septal involvement were significantly older and had lower LVEF than those with isolated free wall LGE. Ten percent (11/113) patients who had LGE died 10.8 months after CMR. Only one patient from the LGE negative group died. Patients who died had higher heart rate, larger left ventricular volume and mass, greater number of positive LGE segment and increase incident of septal LGE compared to those who remained alive. CONCLUSION: In DMD patients, LGE occurs early, is progressive and increases with both age and decreasing LVEF. Segmentally, the incidence of the number of positive LGE segments increase with age and lower LVEF. Older patients and those who died during the study period had more septal LGE involvement. The current studies suggest that the time course and distribution of LGE-positivity may be an important clinical biomarker to aid in the management of DMD-associated cardiac disease.
Hor et al. (Tue,) conducted a observational in Duchenne muscular dystrophy (n=314). Reduced LVEF (<55%) vs. Normal LVEF (≥55%) was evaluated on Presence of late gadolinium enhancement (LGE) (OR 12.3, 95% CI 4.9-30.6, p=<0.0001). In patients with Duchenne muscular dystrophy, late gadolinium enhancement was present in 36% of subjects and its prevalence was significantly higher in those with reduced left ventricular ejection fraction (OR 12.3).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: