Sickle cell disease and ventricular myocardial strain: A systematic review
- PMID: 33742492
- PMCID: PMC9116158
- DOI: 10.1002/pbc.28973
Sickle cell disease and ventricular myocardial strain: A systematic review
Abstract
Cardiac disease is the primary cause of death in sickle cell disease (SCD). Cardiac abnormalities begin in childhood and progress throughout life. Right and left ventricular (RV, LV) myocardial strain are early markers of systolic dysfunction but are not well investigated among individuals with SCD. The objectives of this review were to (1) identify all published studies that have evaluated ventricular myocardial strain, (2) summarize their values, and (3) compare findings with those obtained from controls. From search results of four electronic databases-Medline, Embase, Scopus, and Web of Science-42 potential articles were identified, of which 18 articles and 17 studies met eligibility criteria for inclusion. The evaluated studies demonstrate that RV and LV myocardial strain are generally abnormal in individuals with SCD compared with controls, despite having normal ejection/shortening fraction. Myocardial strain has been inconsistently evaluated in this population and should be considered any time an echocardiogram is performed.
Keywords: global longitudinal strain; heart; sickle cell anemia; speckle tracking; strain.
© 2021 Wiley Periodicals LLC.
Conflict of interest statement
Conflict of interest
J.S.H.received funding from U01HL133996 during conduct of this work and receives research funding from Global Blood Therapeutics and Novartis as well as consulting fees from MJH Life Sciences, Vindico Education, and Global Blood Therapeutics.
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