1. Pathophysiological evaluations of initial plaque development after heart transplantation via serial multimodality imaging and cytokine assessments
- Author
-
Tatsuya Shiraki, Yasuhiro Ichibori, Tomohito Ohtani, Isamu Mizote, Hidetaka Kioka, Yasumasa Tsukamoto, Daisuke Nakamura, Kensuke Yokoi, Seiko Ide, Kei Nakamoto, Yasuharu Takeda, Jun-ichi Kotani, Shungo Hikoso, Yoshiki Sawa, and Yasushi Sakata
- Subjects
Pulmonary and Respiratory Medicine ,Transplantation ,optical coherence tomography ,interleukin-31 ,Coronary Artery Disease ,Allografts ,heart transplantation ,Coronary Vessels ,Plaque, Atherosclerotic ,intravascular ultrasound ,cardiac allograft vasculopathy ,Cytokines ,Humans ,Surgery ,Cardiology and Cardiovascular Medicine ,Tomography, Optical Coherence ,Ultrasonography, Interventional ,Retrospective Studies - Abstract
Shiraki T., Ichibori Y., Ohtani T., et al. Pathophysiological evaluations of initial plaque development after heart transplantation via serial multimodality imaging and cytokine assessments. Journal of Heart and Lung Transplantation 41, 877 (2022); https://doi.org/10.1016/j.healun.2022.03.007., Background: Detailed morphological characteristics of de novo and donor-transmitted plaques and the association of serum T-lymphocyte cytokine levels with plaque progression of coronary allograft vasculopathy within 1 year after heart transplantation are unknown. Methods: In this retrospective analysis of data in a prospectively maintained database, 40 heart transplant recipients were included. We performed serial 3 vessel optical coherence tomography and intravascular ultrasound analyses, at the 8 week (baseline) and 12 month post-transplantation follow-ups, and serum cytokine measurements (n = 23). The correlation between serum cytokines and Δplaque burden (between baseline and follow-up) was evaluated depending on plaque morphology. Results: Thirteen de novo plaques (maximum intimal thickness ≥0.5 mm at the 12 month follow-up without plaques at baseline) were identified in 8 recipients, and 31 donor-transmitted plaques (maximum intimal thickness ≥0.5 mm at baseline) were detected in 17 recipients. Compared with donor-transmitted plaques, the Δplaque burden in the de novo plaques, with mainly fibrous morphology, was high (38.8% [29.6%–41.2%] vs 8.7% [1.33%–13.6%], p < 0.001). Stratification of the morphology of donor-transmitted plaques revealed that the Δplaque burden in fibrous plaques (10.6% [7.0%–18.0%]) was similar to that in fibroatheroma (10.3% [8.7%–23.8%]). Serum interleukin-31 levels at baseline correlated with fibrous plaque proliferation (r = 0.73, p = 0.007) even under immunosuppressive conditions, whereas other cytokines (interleukin-1β, interleukin-17, and interferon-gamma) were mostly undetectable. Conclusions: Intimal fibrous proliferation contributed to the progression of donor-transmitted and de novo plaques. Serum interleukin-31 levels at baseline may contribute to intimal fibrous proliferation within 1 year after heart transplantation.
- Published
- 2022
- Full Text
- View/download PDF