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Updated: Jul 25, 2025

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Clinical characteristics and one-year all-cause mortality outcomes in Africans with dilated cardiomyopathy
Nqoba Tsabedze1, Dineo Mpanya1, Claude Bailly2
1Division of Cardiology, Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Charlotte Maxeke Johannesburg Academic Hospital, Johannesburg, Gauteng, South Africa.
Insights
Dilated cardiomyopathy in sub-Saharan Africa affects young males, leading to heart failure. This study found a 19% one-year mortality rate, highlighting the need for further research into its causes and outcomes.
Area of Science:
- Cardiology
- Public Health
- Sub-Saharan African Medicine
Background:
- Dilated cardiomyopathy (DCM) is a frequent cause of heart failure in sub-Saharan Africa (SSA).
- Patients present with new-onset heart failure with reduced ejection fraction without a clear cause.
- The clinical profile of this specific patient group remains under-characterized.
Purpose of the Study:
- To describe the clinical characteristics of patients experiencing heart failure of unknown origin in SSA.
- To identify potential predictors of mortality and rehospitalization in this cohort.
Main Methods:
- Screening of 161 patients with heart failure of unknown origin.
- Exclusion of known primary and secondary causes of DCM.
- Comprehensive assessment including biochemical testing, echocardiography, cardiovascular magnetic resonance (CMR) imaging, and coronary angiography.
Main Results:
- The study included 93 participants (mean age 47.5 years).
- Late gadolinium enhancement (LGE) was observed in 56.1% of participants, often in the mid-wall.
- A 19% all-cause mortality rate was recorded within a median follow-up of 13.4 months.
- Non-survivors exhibited significantly higher left atrial volume index compared to survivors (p=0.017).
- The rehospitalization rate was 29.3%, with most cases related to heart failure.
Conclusions:
- Dilated cardiomyopathy in Africans predominantly affects young males.
- The disease carries a substantial one-year mortality risk (19%) in this population.
- There is a critical need for large, multicenter studies in SSA to elucidate the pathogenesis and outcomes of DCM.
Aims:
Dilated cardiomyopathy (DCM) is a common cause of heart failure in sub-Saharan Africa (SSA). The affected individuals present with new-onset heart failure with reduced ejection fraction and no identifiable primary or secondary aetiology. We aim to describe the clinical characteristics of participants with heart failure of unknown origin.
Methods:
We screened 161 participants with heart failure of unknown origin and prospectively excluded primary and secondary causes of DCM. All study participants were subjected to laboratory biochemical testing, echocardiography, cardiovascular magnetic resonance (CMR) imaging and invasive coronary angiography.
Results:
The study comprised 93 participants with a mean age of 47.5 SD 13.1 years. Forty-six (56.1%) participants had evidence of late gadolinium enhancement (LGE) on imaging, and LGE was visualised in the mid wall in 28 (61.0%) of these participants. After a median duration of 13.4 months [interquartile range (IQR): 8.8-28.9 months], 18 (19%) participants died. Non-survivors had a higher median left atrial volume index (44.9 mL/m2 (IQR: 34.4-58.7) compared to survivors [32.9 mL/m2 (IQR: 24.5-47.0), p = 0.017)]. The rate of all-cause rehospitalisation was 29.3%, of which 17 of the 22 re-hospitalisations were heart failure related.
Conclusion:
Dilated cardiomyopathy in Africans primarily affects young males. In our cohort, this disease was associated with an all-cause mortality of 19% in one year. In SSA, large multicenter studies are required to investigate this disease's pathogenesis and outcomes.
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