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Prognostic value of late gadolinium enhancement cardiac magnetic resonance in hypertrophic cardiomyopathy: a meta-analysis
© Weng et al. 2016
- Published: 27 January 2016
- Cardiovascular Magnetic Resonance
- Cardiac Magnetic Resonance
- Sudden Cardiac Death
- Late Gadolinium Enhancement
- Hypertrophic Cardiomyopathy
Contrast-enhanced cardiovascular magnetic resonance (CMR) with late gadolinium enhancement (LGE) has emerged as an in vivo marker of myocardial fibrosis, although its significance in identifying high risk hypertrophic cardiomyopathy (HCM) patients remains unresolved. Previous meta-analyses have included studies with data involving overlapping patient populations, thus confounding effect estimates.
We searched PubMed and Web of Science for clinical trials that investigated the prognostic utility of LGE in HCM patients. We excluded studies with overlapping data. Pooled odds ratios (ORs), hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to assess the role of LGE CMR in the risk stratification of HCM patients.
Five studies of unique cohorts were retrieved from 393 citations for the analysis. In total, 2993 patients (mean age = 54.6 years; median follow up = 36.8 months) were included. After synthesizing data, meta-analysis showed that the presence of LGE was associated with a significantly increased risk of sudden cardiac death (SCD)/aborted SCD (pooled OR = 3.42, 95%CI = 1.97-5.94; P < 0.001), cardiac death (pooled OR = 2.93, 95%CI = 1.53-5.61; P = 0.001), all-cause mortality (pooled OR=1.80, 95%CI = 1.21-2.69; P = 0.004), and a trend towards increased risk of heart failure death (pooled OR = 2.21, 95%CI = 0.84-5.80; P = 0.107). Three publications reported results with quantitative LGE. There was a significant relationship between the extent of LGE and risk of SCD (pooled HR 1.56/10% LGE, 95% CI = 1.33-1.82, p < 0.0001), all-cause mortality (pooled HR 1.29/10%LGE, 95% CI = 1.09-1.51, p = 0.002), heart failure mortality (pooled HR 1.61/10% LGE, 95% CI 1.21-2.13, p = 0.001), and cardiovascular mortality (pooled HR 1.57/10% LGE, 95% CI 1.30-1.89, p < 0.001). After adjusting for baseline characteristics, the extent of LGE remained a strong independent predictor for SCD events (pooled HRadjusted 1.36/10%LGE, 95% CI 1.10-1.69, p = 0.005).
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