Predictors of cardiovascular events and all‐cause of death in patients with transfusion‐dependent myelodysplastic syndrome

Male Risk Iron Overload Kaplan-Meier Estimate 03 medical and health sciences 0302 clinical medicine Cause of Death Humans Blood Transfusion Prospective Studies Aged Aged, 80 and over T1 mapping Middle Aged Cardiovascular disease Prognosis Magnetic Resonance Imaging 3. Good health Feature tracking NT-proBNP Cardiovascular Diseases Myelodysplastic Syndromes Female Myelodysplastic syndrome Biomarkers Follow-Up Studies
DOI: 10.1111/bjh.17652 Publication Date: 2021-06-28T09:52:55Z
ABSTRACT
Summary Cardiovascular disease (CVD) involves the second cause of death in low‐risk myelodysplastic syndrome (MDS) population. Prospective study to characterise CVD and identify predictors for combined event (CE) cardiovascular and/or all‐cause mortality transfusion dependent MDS patients. Thirty‐one patients underwent a cardiac assessment including biomarkers magnetic resonance (cMR) with parametric sequences (T1, T2 T2* mapping) myocardial deformation by feature tracking (FT) were analysed clonal hematopoiesis indeterminate potential mutations. Cardiac revealed high prevalence unknown structural heart (51% cMR pathological findings). After 2·2 [0·44] years follow‐up, 35·5% suffered CE: 16% death, 29% event. At multivariate analysis elevated NT‐proBNP ≥ 486pg/ml (HR 96·7; 95%‐CI 1·135–8243; P = 0·044), reduced native T1 time < 983ms 44·8; 1·235–1623; 0·038) higher left ventricular global longitudinal strain (LV‐GLS) 0·4; 0·196–0·973; 0·043) showed an independent prognostic value. These variables, together 20ms, additive value (Log Rank: 12·4; 0·001). In conclusion, frequently suffer CVD. value, relaxation FT are poor prognosis, thus, their determination would high‐risk who could benefit from treatment follow‐up.
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