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Published on: November 5, 2019
Association between pulmonary function and cardiac enzymes in sickle cell disease
Charles Antwi-Boasiako1, Michael M Asare1,2, Ibrahim Baba1
1Department of Physiology, University of Ghana Medical School, University of Ghana Accra, Ghana.
Reduced airflow (FEV1) in sickle cell disease (SCD) patients is linked to elevated cardiac markers (CK-MB). This suggests potential heart muscle damage in individuals with SCD.
Area of Science:
- Cardiology
- Pulmonology
- Hematology
Background:
- Sickle cell disease (SCD) is a multi-organ affecting condition with limited data on lung function and cardiac marker associations.
- Existing research suggests a link between reduced pulmonary function and cardiac dysfunction.
- This study investigates the relationship between pulmonary function and cardiac markers in SCD patients.
Purpose of the Study:
- To examine the association between pulmonary function parameters and cardiac markers in patients with sickle cell disease.
- To identify potential cardiac implications of impaired lung function in SCD.
Main Methods:
- A cross-sectional study comparing 117 SCD patients with 58 healthy controls.
- Genotyping using cellulose acetate electrophoresis.
- Measurement of cardiac enzymes (LDH, CK-MB) and lung function tests (FEV1) using spirometry.
- Lung disease categorization based on Global Lung Initiative criteria.
Main Results:
- Elevated CK-MB and LDH prevalence was higher in SCD patients (76.92% and 9.40%) compared to controls (51.72% and 0%).
- Lung restriction was the most prevalent impairment in both groups (30.77% in SCD, 15.52% in controls).
- Reduced FEV1 was significantly associated with a 3.5-fold increased odds of elevated CK-MB in SCD patients (OR 3.35, p=0.015).
Conclusions:
- Reduced FEV1, indicating airflow impairment, is associated with elevated CK-MB in sickle cell disease patients.
- This association suggests potential cardiomyocyte damage in SCD patients with airflow limitations.
- Further research is warranted to elucidate the mechanisms linking pulmonary and cardiac dysfunction in SCD.
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