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Published on: November 5, 2019
Left ventricular dyssynchrony is an early manifestation of heart involvement in sickle cell anemia
Mehmet Fatih Karakaş1, Eyüp Büyükkaya, Mustafa Kurt
1Department of Cardiology, Tayfur Ata Sokmen Medical School, Mustafa Kemal University, Hatay, Turkey. mfkarakas@hotmail.com
Insights
Sickle cell anemia (SCA) patients show early signs of left ventricular systolic dyssynchrony, even with normal ejection fraction. This indicates potential heart involvement preceding or accompanying diastolic dysfunction.
Area of Science:
- Cardiology
- Hematology
- Medical Imaging
Background:
- Sickle cell anemia (SCA) is a common inherited anemia with known cardiac complications.
- Left ventricular (LV) involvement is established in SCA, but contraction synchrony changes are understudied.
- This study focuses on LV contraction synchrony in SCA patients with normal ejection fraction (EF) and narrow QRS.
Purpose of the Study:
- To investigate left ventricular (LV) contraction synchrony in sickle cell anemia (SCA) patients.
- To identify early cardiac manifestations in SCA patients with preserved EF and narrow QRS.
- To explore the relationship between LV dyssynchrony and other cardiac parameters in SCA.
Main Methods:
- Utilized color-coded tissue Doppler imaging to assess LV dyssynchrony.
- Included 36 SCA patients and 37 matched controls.
- Analyzed various echocardiographic parameters, including systolic and diastolic function indices.
Main Results:
- SCA patients exhibited significantly higher LV systolic dyssynchrony parameters (Ts-SD-12, Ts-12, Ts-SD-6, Ts-6) compared to controls.
- Ventricular dyssynchrony (Ts-SD-12 > 34.4 msec) was present in 55.6% of SCA patients versus 8.1% of controls (P < 0.001).
- Systolic dyssynchrony correlated with hemoglobin, ferritin, LVMI, and diastolic parameters (E/A, Dt, Em).
Conclusions:
- Left ventricular systolic dyssynchrony is an early indicator of cardiac involvement in SCA patients with normal EF and narrow QRS.
- This dyssynchrony may occur concurrently with or precede diastolic dysfunction.
- Tissue Doppler imaging is valuable for detecting early cardiac changes in SCA.
Background:
Sickle cell anemia (SCA) is the most common inherited anemia. Although heart involvement in SCA is well-established, there is no data about changes of contraction synchrony in SCA. Therefore, we aimed to study the left ventricular contraction synchrony in SCA patients with narrow QRS and normal ejection fraction (EF).
Methods:
Thirty-six patients with SCA and 37 age- and gender-matched control subjects were included in the study. Left ventricular dyssynchrony was investigated by color-coded tissue Doppler imaging.
Results:
The SCA patients had lower hemoglobin (Hb) and higher ferritin, left ventricular end-diastolic diameter, left ventricular end-systolic diameter, left ventricular mass index (LVMI), and pulmonary artery pressure. Peak A velocity, Dt, and E/E' values were higher in the SCA group however, E/A ratio and average Em were higher in the control group. LV systolic dyssynchrony parameters including Ts-SD-12, Ts-12, Ts-SD-6, and Ts-6 were found to be higher in SCA group when compared with controls. In addition to that, the patients with ventricular dyssynchrony (a Ts-SD-12 > 34.4 msec) were higher in the SCA group than the control group (55.6% vs. 8.1%, P < 0.001). In the correlation analysis, systolic dyssynchrony parameters were found to be correlated with Hb, ferritin, LVMI, E/A, Dt, Em.
Conclusion:
Our results revealed that in SCA patients with normal EF and narrow QRS, left ventricular systolic dyssynchrony was an early manifestation of heart involvement and might be coexisted with or preceding diastolic dysfunction.
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