Key result
Pediatric hematopoietic stem cell transplantation was associated with decreased left ventricular diastolic function in young adulthood, evidenced by a higher estimated LV filling pressure (E/Ea 9.92 vs 7.24) compared to healthy controls.
Why the study?
Little is known regarding the value of CMR for early identification of high-risk patients after pediatric HSCT before symptomatic cardiovascular disease manifests.
Does a history of pediatric hematopoietic stem cell transplantation alter CMR-derived left ventricular function, aortic stiffness, or myocardial tissue characteristics in young adults compared to healthy controls?
Cross-Sectional (n=32)
Single-blind
No
Does a history of pediatric hematopoietic stem cell transplantation alter CMR-derived left ventricular function, aortic stiffness, or myocardial tissue characteristics in young adults compared to healthy controls?
Absolute Event Rate: 9.92% vs 7.24%
p-value: p=0.004
Young adults with a history of pediatric HSCT show subclinical impairments in LV diastolic function on CMR, highlighting the potential value of E/Ea assessment for early detection of cardiovascular risk in this population.
May warrant diastolic surveillance in young HSCT survivors; leaves open whether findings predict events or warrant intervention.
Pediatric hematopoietic stem cell transplantation (HSCT) recipients are at increased risk of cardiovascular disease later in life. As HSCT survival has significantly improved, with a growing number of HSCT indications, tailored screening strategies for HSCT-related late effects are warranted. Little is known regarding the value of cardiovascular magnetic resonance (CMR) for early identification of high-risk patients after HSCT, before symptomatic cardiovascular disease manifests. This study aimed to assess CMR-derived left ventricular (LV) systolic and diastolic function, aortic stiffness and myocardial tissue characteristics in young adults who received HSCT during childhood. Sixteen patients (22.1 ± 1.5 years) treated with HSCT during childhood and 16 healthy controls (22.1 ± 1.8 years) underwent 3 T CMR. LV systolic and diastolic function were measured as LV ejection fraction (LVEF), the ratio of transmitral early and late peak filling rate (E/A), the estimated LV filling pressure (E/Ea) and global longitudinal and circumferential systolic strain and diastolic strain rates, using balanced steady-state free precession cine CMR and 2D velocity-encoded CMR over the mitral valve. Aortic stiffness, myocardial fibrosis and steatosis were assessed with 2D velocity-encoded CMR, native T1 mapping and proton CMR spectroscopy (1H-CMRS), respectively. In the patient compared to the control group, E/Ea (9.92 ± 3.42 vs. 7.24 ± 2.29, P = 0.004) was higher, LVEF (54 ± 6% vs. 58 ± 5%, P = 0.055) and global longitudinal strain (GLS) ( -20.7 ± 3.5% vs. -22.9 ± 3.0%, P = 0.063) tended to be lower, while aortic pulse wave velocity (4.40 ± 0.26 vs. 4.29 ± 0.29 m/s, P = 0.29), native T1 (1211 ± 36 vs. 1227 ± 28 ms, P = 0.16) and myocardial triglyceride content (0.47 ± 0.18 vs. 0.50 ± 0.13%, P = 0.202) were comparable. There were no differences between patients and controls in E/A (2.76 ± 0.92 vs. 2.97 ± 0.91, P = 0.60) and diastolic strain rates. In young adults who received HSCT during childhood, LV diastolic function was decreased (higher estimated LV filling pressure) and LV systolic function (LVEF and GLS) tended to be reduced as compared to healthy controls, whereas no concomitant differences were found in aortic stiffness and myocardial tissue characteristics. When using CMR, assessment of LV diastolic function in particular is important for early detection of patients at risk of HSCT-related cardiovascular disease, which may warrant closer surveillance.
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Paiman et al. (2019) conducted a cross-sectional in Pediatric hematopoietic stem cell transplantation (n=32). Pediatric hematopoietic stem cell transplantation vs. Healthy controls was evaluated on Estimated LV filling pressure (E/Ea) (p=0.004). Pediatric hematopoietic stem cell transplantation was associated with decreased left ventricular diastolic function in young adulthood, evidenced by a higher estimated LV filling pressure (E/Ea 9.92 vs 7.24) compared to healthy controls.
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