Key result
Allogeneic HCT linked to ~74% higher 90-day incidence of AF compared to autologous HCT.
Why the study?
The incidence and risk factors for early-onset atrial fibrillation following hematopoietic cell transplant remain poorly understood.
Does allogeneic hematopoietic cell transplant increase the risk of early-onset atrial fibrillation compared to autologous transplant in patients without prior cardiovascular disease?
Cohort (n=5,965)
No
Does allogeneic hematopoietic cell transplant increase the risk of early-onset atrial fibrillation compared to autologous transplant in patients without prior cardiovascular disease?
Allogeneic transplant recipients have a significantly higher risk of early-onset atrial fibrillation compared to autologous recipients, particularly those with older age, lower performance status, or obesity, warranting closer post-transplant monitoring.
Answers are grounded in this paper and cite their sources.
Elevated early AF risk after alloHCT may support targeted monitoring; extends observational incidence data in a large contemporary cohort.
Introduction Atrial fibrillation (AF) is the most common acute cardiovascular complication following hematopoietic cell transplant (HCT). However, the incidence and risk factors for early-onset AF post-HCT remain poorly understood. Methods A retrospective cohort study was conducted to assess the onset and risk factors of AF within 90 days post-HCT in 5,965 adult transplant recipients. Patients underwent either allogeneic HCT (alloHCT, n = 2,742) or autologous HCT (autoHCT, n = 3,223) between January 1st, 2010 and December 31st, 2023. Cumulative incidence curves and Gray’s tests were used to assess AF cumulative incidence. Fine-Gary proportional sub-distributional hazard models were applied to estimate associations between factors and AF risk. Results Among patients without prior arrhythmia, cardiac disease, or valvular heart disease, AF occurred more frequently in alloHCT recipients than in autoHCT recipients (6.3% vs. 4.3%, Gray’s test P < 0.001). The median age was 54 years (range: 18–82) for alloHCT and 59 years (range: 18–78) for autoHCT. In alloHCT recipients, increased AF risk was associated with older age (≥ 50 vs. <50 years, adjusted hazard ratio (HR) = 2.85, P < 0.0001) and lower Karnofsky performance score (KPS, < 80 vs. ≥80, adjusted HR = 1.69, P = 0.03). In autoHCT recipients, increased AF risk was associated with older age (adjusted HR = 2.49, P = 0.006), lower KPS (adjusted HR = 2.41, P = 0.0001) and obesity (adjusted HR = 1.68, P = 0.015). Conclusion(s) This study indicates that AF cumulative incidence within 90 days post-HCT is higher in alloHCT than in autoHCT patients. Transplant recipients with older age, lower KPS, or obesity have an increased risk for early onset of AF post-HCT.
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Cai et al. (2026) conducted a cohort in Hematopoietic stem cell transplant recipients (n=5,965). Allogeneic hematopoietic cell transplant (alloHCT) vs. Autologous hematopoietic cell transplant (autoHCT) was evaluated on Cumulative incidence of atrial fibrillation within 90 days post-transplant (HR 1.74, 95% CI 1.39-2.19, p=<0.0001). Allogeneic hematopoietic cell transplant was associated with a higher 90-day cumulative incidence of atrial fibrillation compared to autologous transplant (6.3% vs. 4.3%; adjusted HR 1.74, p<0.0001).
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