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Left ventricular systolic function in sickle cell anemia: a meta-analysis
Shyam Poludasu1, Keshwar Ramkissoon, Louis Salciccioli
1Division of Cardiovascular Medicine, Department of Medicine, State University of New York, Downstate Medical Center, Brooklyn, New York, USA.
Patients with sickle cell anemia (SCA) show normal load-dependent left ventricular (LV) systolic function but impaired load-independent function. SCA is linked to progressive LV dilation and dysfunction with age.
Area of Science:
- Cardiology
- Hematology
- Medical Research
Background:
- Sickle cell anemia (SCA) is a genetic blood disorder.
- Potential impact of SCA on cardiac function requires evaluation.
Purpose of the Study:
- To assess for left ventricular (LV) systolic dysfunction in patients with SCA.
Main Methods:
- Systematic literature review of Medline, Embase, Ebscohost, and Google Scholar.
- Included studies comparing LV function measures (EF, FS, CI) between SCA patients and controls.
- Analyzed 19 studies with 841 SCA patients and 554 controls.
Main Results:
- No significant difference in LV ejection fraction (LVEF) or fractional shortening (FS) between SCA patients and controls.
- Cardiac index (CI) was higher, and LV end-systolic stress-volume index was lower in SCA patients.
- LV dimensions were larger in SCA patients and increased with age; all measures correlated inversely with age.
Conclusions:
- SCA patients exhibit normal load-dependent LV systolic function but reduced load-independent function.
- SCA is associated with LV dilation, which progresses with age.
- Age-dependent LV structural and functional abnormalities are observed in SCA.
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