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Case-control study reveals elevated MMP-9 correlates with myocardial iron overload in sickle cell disease, indicating its utility as a biomarker for cardiac risk.
Background Cardiac iron overload is secondary to chronic blood transfusion in patients with sickle cell disease (SCD). Iron overload cardiomyopathy is a restrictive cardiomyopathy associated with systolic and diastolic dysfunction. Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases responsible for tissue remodeling. Many studies offer strong evidence for the role of MMP-9 in left ventricular (LV) remodeling. Objective The authors aimed to detect the plasma levels of MMP-9 in patients with SCD and its relationship to myocardial iron overload. Materials and methods A case–control study was carried out on 75 patients with SCD and 75 age-matched and sex-matched healthy controls. Assessment of cardiac iron overload in patients by MRI T2* was performed. Plasma MMP-9 levels were measured for patients and controls using enzyme-linked immunosorbent assay. Results Patients with SCD had significantly higher levels of MMP-9 than controls. There was a highly significant relationship between plasma levels of MMP-9 and each of cardiac T2* and serum ferritin. Patients with vaso-occlusive crises (VOC) greater than 5/year had significantly higher levels of MMP-9 than those with VOC less than or equal to 5 /year. Conclusion MMP-9 seems to be a useful marker in patients with SCD. Patients with cardiac T2* less than 20 ms, serum ferritin greater than 1000 ng/ml, and recurrent VOC greater than 5/year had significantly higher MMP-9 serum levels than others.
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Badr et al. (2022) studied this question.
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