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Published on: July 12, 2024
Progression of cardiac allograft vasculopathy assessed by serial three-vessel quantitative coronary angiography
Christian Zanchin1, Kyohei Yamaji1, Carolin Rogge1
1Department of Cardiology, Bern University Hospital, Bern, Switzerland.
Insights
Cardiac allograft vasculopathy (CAV) progresses significantly after heart transplantation, even in patients without early visual signs. Quantitative coronary angiography (QCA) confirms long-term CAV progression, though it may not predict it beyond one year.
Area of Science:
- Cardiology
- Transplantation Immunology
- Vascular Biology
Background:
- Cardiac allograft vasculopathy (CAV) is a major long-term complication after heart transplantation.
- Assessing CAV progression is crucial for patient management and outcomes.
Purpose of the Study:
- To evaluate the short- and long-term progression of CAV using serial 3-vessel quantitative coronary angiography (QCA).
Main Methods:
- Serial 3-vessel QCA was performed at baseline, 1-year, and long-term follow-up (8.5±3.7 years) post-heart transplantation.
- Changes in minimal lumen diameter (MLD) and percent diameter stenosis (%DS) were analyzed in matched segments.
- Patients were classified using the ISHLT-CAV criteria (ISHLT-CAV0 vs. ISHLT-CAV1-3).
Main Results:
- MLD significantly decreased from 1-year to long-term follow-up (Δ-0.08mm/year, P<0.001).
- %DS significantly increased from baseline to 1-year (Δ+0.96%/year, P=0.041) and from 1-year to long-term follow-up (Δ+0.61%/year, P<0.001).
- CAV progression occurred similarly in ISHLT-CAV0 and ISHLT-CAV1-3 groups between baseline and long-term follow-up.
Conclusions:
- QCA confirms CAV progression beyond one year post-transplant.
- CAV progresses to a similar extent in patients with and without early visual signs of CAV.
- QCA may not be predictive of CAV beyond the first year.
Background:
The purpose of the present study was to assess the short- and long-term progression of cardiac allograft vasculopathy (CAV) using serial 3-vessel quantitative coronary angiography (QCA).
Methods:
CAV progression was assessed using serial 3-vessel QCA analysis at baseline, 1-year and long-term angiographic follow-up (8.5±3.7 years) after heart transplantation. The change in minimal lumen diameter (MLD) and percent diameter stenosis (%DS) was serially assessed within matched segments. Patients were graded according to the ISHLT-CAV classification and grouped as ISHLT-CAV0 and ISHLT-CAV1-3. The primary endpoint was mean change in MLD and %DS.
Results:
A total of 41 patients and 520 matched segments were available for serial 3-vessel QCA. Overall, MLD decreased non-significantly from baseline to 1-year follow-up and significantly from 1-year to the long-term angiographic follow-up (Δ-0.08mm/year [95%CI -0.11 to -0.05], P<0.001). %DS increased significantly from baseline to 1-year (Δ+0.96%/year [95%CI 0.04 to 1.88], P = 0.041) and from 1-year to long-term angiographic follow-up (Δ+0.61%/year [95%CI 0.33 to 0.88], P<0.001). ISHLT-CAV1-3 at 1 year and at long-term angiographic follow-up was observed in 22% and 61%, respectively. Between baseline and long-term angiographic follow-up, a significant reduction in MLD was observed within both groups without a significant difference in the reduction between the two groups (ISHLT-CAV0: median -0.49mm [IQR -0.54 to -0.43] vs. ISHLT-CAV1-3: median -0.40mm [IQR -0.44 to -0.35], P = 0.4).
Conclusion:
The current data suggest that QCA can't predict CAV beyond 1 year, but, QCA affirmed that CAV progresses to a similar extent in patients who do not develop visual CAV during long-term follow-up.
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