Abstract

Background: Several studies conducted in America or Europe have described major cardiac remodeling and diastolic dysfunction in patients with sickle cell disease (SCD). We aimed at assessing cardiac involvement in SCD in sub-Saharan Africa where SCD is the most prevalent.Methods: In Cameroon, Mali and Senegal, SCD patients and healthy controls of the CADRE study underwent transthoracic echocardiography if aged ≥10 years. The comparison of clinical and echocardiographic features between patients and controls, and the associations between echocardiographic features and the vascular complications of SCD were assessed.Results: 612 SCD patients (483 SS or Sβ0, 99 SC, and 19 Sβ+) and 149 controls were included. The prevalence of dyspnea and congestive heart failure was low and did not differ significantly between patients and controls. While left ventricular ejection fraction did not differ between controls and patients, left and right cardiac chambers were homogeneously more dilated and hypertrophic in patients compared to controls and systemic vascular resistances were lower (p < 0.001 for all comparisons). Three hundred and forty nine SCD patients had extra-cardiac organ damages (stroke, leg ulcer, priapism, microalbuminuria or osteonecrosis). Increased left ventricular mass index, cardiac dilatation, cardiac output, and decreased systemic vascular resistances were associated with a history of at least one SCD-related organ damage after adjustment for confounders.Conclusions: Cardiac dilatation, cardiac output, left ventricular hypertrophy, and systemic vascular resistance are associated with extracardiac SCD complications in patients from sub-Saharan Africa despite a low prevalence of clinical heart failure. The prognostic value of cardiac subclinical involvement in SCD patients deserves further studies.

Highlights

  • Sickle cell disease (SCD) is a hemoglobin genetic disorder responsible for deep chronic hemolytic anemia, recurrent acute vaso-occlusive crises, and chronic vasculopathy leading to multiple organ failure such as glomerulopathy, osteonecrosis, leg ulcers, stroke, pulmonary hypertension, and priapism

  • The overall aim of CADRE is to provide descriptive and prognostic data in SCD patients living in sub-Saharan Africa, especially regarding the cardiovascular complications of SCD

  • The objective of the present study is to determine the prevalence of cardiac involvement in African SCD patients and attempt to identify factors associated with adverse outcomes

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Summary

Introduction

Sickle cell disease (SCD) is a hemoglobin genetic disorder responsible for deep chronic hemolytic anemia, recurrent acute vaso-occlusive crises, and chronic vasculopathy leading to multiple organ failure such as glomerulopathy, osteonecrosis, leg ulcers, stroke, pulmonary hypertension, and priapism. Both chronic anemia and myocardial ischemia are known to lead to heart failure in the general population (1). We analyzed the clinical and echocardiographic data of the patients included in the CADRE study to assess the frequency of SCD-related cardiac abnormalities in sub-Saharan Africa and looked for associations between cardiac involvement and other SCD-related organ damage. We aimed at assessing cardiac involvement in SCD in sub-Saharan Africa where SCD is the most prevalent

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