Prevalence of left ventricular diastolic dysfunction by cardiac magnetic resonance imaging in thalassemia major patients with normal left ventricular systolic function
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Published on: December 13, 2019
Benjaporn Chinprateep1, Nithima Ratanasit1, Yodying Kaolawanich1
1Division of Cardiology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkoknoi, Bangkok, 10700, Thailand.
Insights
Left ventricular diastolic dysfunction (LVDD) affects 20.7% of thalassemia major patients before cardiac iron overload is detected. Homozygous beta-thalassemia and splenectomy are key predictors, highlighting the need for early LVDD screening.
Area of Science:
- Cardiology
- Hematology
- Medical Imaging
Background:
- Iron overload cardiomyopathy is the primary cause of mortality in thalassemia major patients.
- Early detection of left ventricular diastolic dysfunction (LVDD) before systolic dysfunction may improve patient prognosis.
- This study investigates the prevalence and associated factors of LVDD in thalassemia major patients with preserved systolic function.
Purpose of the Study:
- To determine the prevalence of LVDD in thalassemia major patients with normal left ventricular systolic function.
- To identify factors associated with LVDD in this patient population.
- To inform early diagnostic strategies and improve outcomes for thalassemia major patients.
Main Methods:
- Cardiac magnetic resonance (CMR) imaging, specifically T2* sequences, was used to assess cardiac iron levels.
- Left ventricular diastolic function was evaluated using mitral valve filling parameters and left atrial volume index.
- Adult patients with thalassemia major and normal systolic function were included, excluding those with significant valvular or pericardial disease.
Main Results:
- The prevalence of LVDD was 20.7% among the 116 included patients.
- Cardiac T2* was abnormal in 7.8% of patients, indicating iron overload.
- Multivariate analysis identified age, body surface area, homozygous beta-thalassemia, splenectomy, heart rate, and diastolic blood pressure as significant factors associated with LVDD.
Conclusions:
- LVDD is present in early stages of thalassemia major, often preceding detectable cardiac iron overload (abnormal T2*).
- Homozygous beta-thalassemia and splenectomy emerged as strong predictors of LVDD.
- Findings emphasize the importance of increased awareness and early screening for LVDD in high-risk thalassemia major patient groups.
Background:
The leading cause of mortality of thalassemia major patients is iron overload cardiomyopathy. Early diagnosis with searching for left ventricular diastolic dysfunction before the systolic dysfunction ensued might yield better prognosis. This study aimed to define the prevalence of the left ventricular diastolic dysfunction (LVDD) in thalassemia major patients with normal left ventricular systolic function and the associated factors.
Methods:
Adult thalassemia major patients with normal left ventricular systolic function who were referred for cardiac T2* at Siriraj Hospital - Thailand's largest national tertiary referral center - during the October 2014 to January 2017 study period. Left ventricular diastolic function was defined by mitral valve filling parameters and left atrial volume index using CMR. Patients with moderate to severe valvular heart disease, pericardial disease, or incomplete data were excluded. Baseline characteristics, comorbid diseases, current medication, and laboratory results were recorded and analyzed.
Results:
One hundred and sixteen patients were included, with a mean age of 27.5 ± 13.5 years, 57.8% were female, and 87.9% were transfusion dependent. Proportions of homozygous beta-thalassemia and beta-thalassemia hemoglobin E were 12.1 and 87.9%, respectively. The baseline hematocrit was 26.3 ± 3.3%. The prevalence of LVDD was 20.7% (95% CI: 13.7-29.2%). Cardiac T2* was abnormal in 7.8% (95% CI: 3.6-14.2%). Multivariate analysis revealed age, body surface area, homozygous beta-thalassemia, splenectomy, heart rate, and diastolic blood pressure to be significantly associated with LVDD.
Conclusions:
LVDD already exists from the early stages of the disease before the abnormal heart T2 * is detected. Homozygous beta-thalassemia and splenectomy were strong predictors of LVDD. These data may increase awareness of the disease, especially in the high risk groups.
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