Cardiac allograft vasculopathy: Differences of absolute and relative intimal hyperplasia in children versus adults in optical coherence tomography.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 04 2021
Historique:
received: 24 09 2020
revised: 01 12 2020
accepted: 04 12 2020
pubmed: 15 12 2020
medline: 29 5 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

Intracoronary imaging enables an early detection of intimal changes. To what extend the development of absolute and relative intimal hyperplasia in intracoronary imaging differs depending on age and post-transplant time is not known. Aim of our retrospective study was to compare findings between 24 pediatric (cohort P) and 21 adult HTx patients (cohort A) using optical coherence tomography (OCT) at corresponding post-transplant intervals (≤5 years: P1 (n = 11) and A1 (n = 10); >5 and ≤ 10 years: P2 (n = 13) and A2 (n = 11),. Coronary intima thickness (IT), media thickness (MT) and intima to media ratio (I/M) were assessed per quadrant. Maximal IT >0.3 mm was considered absolute, I/M > 1 relative intimal hyperplasia. Compared to A1, I/M was significantly higher in P1 (maximal I/M: P1: 5.41 [2.81-13.39] vs. A1: 2.30 [1.55-3.62], p = 0.005), whereas absolute IT values were comparable. In contrast, I/M was comparable between P2 and A2, but absolute IT were significantly higher in A2 (maximal IT: P2: 0.16 mm [0.11-0.25] vs. A2: 0.40 mm [0.30-0.71], p < 0.001). A2 presented with higher absolute IT (maximal: A1: 0.16 mm [0.12-0.44] vs. A2: 0.40 mm [0.30-0.71], p = 0.02) and I/M (maximal I/M A1: 2.30 [1.55-3.62] vs. A2: 3.79 [3.01-5.62], p = 0.04). Our results suggest an age- and time-dependent difference in the prevalence of absolute and relative intimal hyperplasia in OCT, with an early peak in children and a progressive increase in adults.

Sections du résumé

BACKGROUND
Intracoronary imaging enables an early detection of intimal changes. To what extend the development of absolute and relative intimal hyperplasia in intracoronary imaging differs depending on age and post-transplant time is not known.
METHODS
Aim of our retrospective study was to compare findings between 24 pediatric (cohort P) and 21 adult HTx patients (cohort A) using optical coherence tomography (OCT) at corresponding post-transplant intervals (≤5 years: P1 (n = 11) and A1 (n = 10); >5 and ≤ 10 years: P2 (n = 13) and A2 (n = 11),. Coronary intima thickness (IT), media thickness (MT) and intima to media ratio (I/M) were assessed per quadrant. Maximal IT >0.3 mm was considered absolute, I/M > 1 relative intimal hyperplasia.
RESULTS
Compared to A1, I/M was significantly higher in P1 (maximal I/M: P1: 5.41 [2.81-13.39] vs. A1: 2.30 [1.55-3.62], p = 0.005), whereas absolute IT values were comparable. In contrast, I/M was comparable between P2 and A2, but absolute IT were significantly higher in A2 (maximal IT: P2: 0.16 mm [0.11-0.25] vs. A2: 0.40 mm [0.30-0.71], p < 0.001). A2 presented with higher absolute IT (maximal: A1: 0.16 mm [0.12-0.44] vs. A2: 0.40 mm [0.30-0.71], p = 0.02) and I/M (maximal I/M A1: 2.30 [1.55-3.62] vs. A2: 3.79 [3.01-5.62], p = 0.04).
CONCLUSION
Our results suggest an age- and time-dependent difference in the prevalence of absolute and relative intimal hyperplasia in OCT, with an early peak in children and a progressive increase in adults.

Identifiants

pubmed: 33316256
pii: S0167-5273(20)34273-X
doi: 10.1016/j.ijcard.2020.12.025
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

227-234

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Dr. S. Ulrich used retrospectively some OCT data that had also been previously used in a prospective study supported by Novartis Pharma GmbH. Novartis Pharma GmbH was not involved in the development, realization and data analysis of this study. Dr. S. Ulrich has also received financial research support from Astellas Pharma GmbH, “Verein zur Förderung von Wissenschaft und Forschung“(medical faculty of Ludwig-Maximilians-University Munich, Germany) and currently receives financial research support from Gerd-Killian Projektförderung (DGPK, “Deutsche Herzstiftung”, Germany). Dr. Braun reports speaker honoraria from Abbott Vascular. Dr. Hausleiter reports grants and personal fees from Abbott Vascular, grants and personal fees from Edwards Lifesciences, outside the submitted work. Dr. Massberg reports grants from German Federal Ministry of Education and Research (BMBF)/German Center for Cardiovascular Research (DZHK), grants from German Research Foundation (DFG), grants from Boston scientific, grants from Foundation Leduq Transatlantic Network of Excellence, outside the submitted work. Dr. Mehilli received funding of German Centre for Cardiovascular Research (DZHK) for material costs of optical coherence tomography and image analysis. The authors report no relationships that could be construed as a conflict of interest.

Auteurs

Madeleine Orban (M)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany; Partner Site Munich Heart Alliance, German Centre for Cardiovascular Research (DZHK), Germany. Electronic address: Madeleine.Orban@med.uni-muenchen.de.

Sarah Ulrich (S)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Dominic Dischl (D)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Patrick von Samson-Himmelstjerna (P)

Department of Heart Surgery, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

René Schramm (R)

Department of Heart Surgery, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Katharina Tippmann (K)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Ralph Hein-Rothweiler (R)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Anna Strüven (A)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Anja Lehner (A)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Daniel Braun (D)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Jörg Hausleiter (J)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany; Partner Site Munich Heart Alliance, German Centre for Cardiovascular Research (DZHK), Germany.

Andre Jakob (A)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Marcus Fischer (M)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Christian Hagl (C)

Department of Heart Surgery, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany; Partner Site Munich Heart Alliance, German Centre for Cardiovascular Research (DZHK), Germany.

Nikolaus Haas (N)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

Steffen Massberg (S)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany; Partner Site Munich Heart Alliance, German Centre for Cardiovascular Research (DZHK), Germany.

Julinda Mehilli (J)

Department of Cardiology, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany; Partner Site Munich Heart Alliance, German Centre for Cardiovascular Research (DZHK), Germany.

Dalla Pozza Robert (DP)

Department of Pediatric Cardiology and Intensive Care Medicine, Ludwig-Maximilians-University, Klinikum Großhadern, Munich, Germany.

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