Key result
Higher baseline cTnI linked to ~123% greater early LVEF decline risk per doubling during HSCT.
Why the study?
Intensive conditioning regimens during HSCT may impose substantial cardiac stress, but early cardiac functional changes during the peri-transplant period remain poorly characterized under protective isolation conditions.
Observational (n=56)
No
Odds Ratio: 2.23 (95% CI 1.12–4.45)
p-value: p=0.023
Early transient left ventricular systolic dysfunction occurs during the immediate peri-transplant period of HSCT, and baseline cardiac troponin I levels can help identify patients at higher risk for this early functional impairment.
Early transient cardiac changes may occur during HSCT; hypothesis-generating for cTnI-guided monitoring in prospective trials.
Patients undergoing hematopoietic stem cell transplantation (HSCT) are exposed to intensive conditioning regimens that may impose substantial cardiac stress during the peri-transplant period; however, early cardiac functional changes during this phase remain poorly characterized, particularly under protective isolation conditions that limit routine imaging. In this prospective observational study, 56 adult HSCT recipients underwent serial bedside transthoracic echocardiography performed before conditioning (pre), on the day of transplantation (t0), 5 days post-transplantation (t5), and at engraftment (eng). Early cardiac functional decline was defined as a ≥ 10% reduction in left ventricular ejection fraction (LVEF) from baseline. LVEF showed a modest but significant transient decline during the early post-transplant period, reaching a nadir at day 5, with partial recovery thereafter. In multivariable analyses, higher baseline cardiac troponin I (cTnI) levels were associated with greater early LVEF decline. An exploratory model incorporating baseline cTnI, N-terminal pro-B-type natriuretic peptide (NT-proBNP), and age demonstrated moderate discrimination for early LVEF decline (AUC = 0.741) and a high negative predictive value (90.9%). These findings suggest that early transient cardiac functional alterations may occur during HSCT, and that baseline cTnI may help identify patients at low risk for early functional impairment. Validation in larger cohorts is warranted.
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Jiang et al. (2026) conducted an observational in Hematological diseases requiring hematopoietic stem cell transplantation (n=56). Baseline cardiac troponin I (cTnI) vs. Lower baseline cTnI levels was evaluated on Early LVEF decline (≥ 10% reduction in LVEF from baseline at day 5 post-transplantation) (OR 2.23, 95% CI 1.12-4.45, p=0.023). Higher baseline cardiac troponin I levels were independently associated with an increased risk of early left ventricular ejection fraction decline during hematopoietic stem cell transplantation (OR 2.23 per doubling of cTnI).
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