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
AUTHORS (10)
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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