Progression of cardiac allograft vasculopathy assessed by serial three-vessel quantitative coronary angiography

PLoS One. 2018 Aug 27;13(8):e0202950. doi: 10.1371/journal.pone.0202950. eCollection 2018.

Abstract

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.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allografts
  • Cardiac Imaging Techniques / methods
  • Continuity of Patient Care*
  • Coronary Angiography / methods*
  • Disease Progression
  • Female
  • Graft Occlusion, Vascular / diagnostic imaging*
  • Graft Occlusion, Vascular / etiology
  • Graft Rejection / etiology
  • Graft Rejection / prevention & control
  • Heart Diseases / surgery*
  • Heart Transplantation / adverse effects*
  • Humans
  • Male
  • Middle Aged
  • Postoperative Complications / diagnostic imaging*
  • Retrospective Studies
  • Risk Assessment
  • Vascular Diseases / diagnostic imaging*
  • Vascular Diseases / etiology

Grants and funding

TZ is funded by an MD-PhD Grant from the Swiss National Science Foundation (grant no. 323530_171146). The study was supported by research grants from Bern University Hospital. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.