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Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis
BACKGROUND: The influence of preexisting donor-transmitted atherosclerosis (DA) on cardiac allograft vasculopathy (CAV) development remains unclear. METHODS: We performed 3-dimensional intravascular ultrasound (3D-IVUS) analysis in 42 heart transplantation (HTx) recipients at 2.1 ± 0.9 months (basel...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441888/ https://www.ncbi.nlm.nih.gov/pubmed/27472091 http://dx.doi.org/10.1097/TP.0000000000001322 |
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author | Watanabe, Takuya Seguchi, Osamu Yanase, Masanobu Fujita, Tomoyuki Murata, Yoshihiro Sato, Takuma Sunami, Haruki Nakajima, Seiko Kataoka, Yu Nishimura, Kunihiro Hisamatsu, Eriko Kuroda, Kensuke Okada, Norihiro Hori, Yumiko Wada, Kyoichi Hata, Hiroki Ishibashi-Ueda, Hatsue Miyamoto, Yoshihiro Fukushima, Norihide Kobayashi, Junjiro Nakatani, Takeshi |
author_facet | Watanabe, Takuya Seguchi, Osamu Yanase, Masanobu Fujita, Tomoyuki Murata, Yoshihiro Sato, Takuma Sunami, Haruki Nakajima, Seiko Kataoka, Yu Nishimura, Kunihiro Hisamatsu, Eriko Kuroda, Kensuke Okada, Norihiro Hori, Yumiko Wada, Kyoichi Hata, Hiroki Ishibashi-Ueda, Hatsue Miyamoto, Yoshihiro Fukushima, Norihide Kobayashi, Junjiro Nakatani, Takeshi |
author_sort | Watanabe, Takuya |
collection | PubMed |
description | BACKGROUND: The influence of preexisting donor-transmitted atherosclerosis (DA) on cardiac allograft vasculopathy (CAV) development remains unclear. METHODS: We performed 3-dimensional intravascular ultrasound (3D-IVUS) analysis in 42 heart transplantation (HTx) recipients at 2.1 ± 0.9 months (baseline) and 12.2 ± 0.4 months post-HTx, as well as consecutive 3D-IVUS analyses up to 3 years post-HTx in 35 of the 42 recipients. Donor-transmitted atherosclerosis was defined as a maximal intimal thickness of 0.5 mm or greater at baseline. Changes in volumetric IVUS parameters were compared in recipients with (DA group) and without DA (DA-free group) at baseline, 1 year, and 3 years post-HTx. RESULTS: Donor-transmitted atherosclerosis was observed in 57.1% of 42 recipients. The DA group exhibited a significantly greater increase in plaque volume at 1 year post-HTx (P < 0.001), leading to increased percent plaque volume (plaque volume/vessel volume, [%]) (P < 0.001) and decreased luminal volume (P = 0.021). Donor-transmitted atherosclerosis was independently associated with a greater increase in percent plaque volume during the first post-HTx year (P = 0.011). From 1 to 3 years post-HTx, the DA group underwent continuous reduction in luminal volume (P = 0.022). These changes resulted in a higher incidence of angiographic CAV at 3 years post-HTx in the DA group (58.8% vs 5.6%, P = 0.002). CONCLUSIONS: This volumetric IVUS study suggests that DA correlates with the worsening change in CAV several years post-HTx. Donor-transmitted atherosclerosis recipients may require more aggressive treatment to prevent subsequent CAV progression. |
format | Online Article Text |
id | pubmed-5441888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-54418882017-06-02 Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis Watanabe, Takuya Seguchi, Osamu Yanase, Masanobu Fujita, Tomoyuki Murata, Yoshihiro Sato, Takuma Sunami, Haruki Nakajima, Seiko Kataoka, Yu Nishimura, Kunihiro Hisamatsu, Eriko Kuroda, Kensuke Okada, Norihiro Hori, Yumiko Wada, Kyoichi Hata, Hiroki Ishibashi-Ueda, Hatsue Miyamoto, Yoshihiro Fukushima, Norihide Kobayashi, Junjiro Nakatani, Takeshi Transplantation Original Clinical Science—General: Outcomes BACKGROUND: The influence of preexisting donor-transmitted atherosclerosis (DA) on cardiac allograft vasculopathy (CAV) development remains unclear. METHODS: We performed 3-dimensional intravascular ultrasound (3D-IVUS) analysis in 42 heart transplantation (HTx) recipients at 2.1 ± 0.9 months (baseline) and 12.2 ± 0.4 months post-HTx, as well as consecutive 3D-IVUS analyses up to 3 years post-HTx in 35 of the 42 recipients. Donor-transmitted atherosclerosis was defined as a maximal intimal thickness of 0.5 mm or greater at baseline. Changes in volumetric IVUS parameters were compared in recipients with (DA group) and without DA (DA-free group) at baseline, 1 year, and 3 years post-HTx. RESULTS: Donor-transmitted atherosclerosis was observed in 57.1% of 42 recipients. The DA group exhibited a significantly greater increase in plaque volume at 1 year post-HTx (P < 0.001), leading to increased percent plaque volume (plaque volume/vessel volume, [%]) (P < 0.001) and decreased luminal volume (P = 0.021). Donor-transmitted atherosclerosis was independently associated with a greater increase in percent plaque volume during the first post-HTx year (P = 0.011). From 1 to 3 years post-HTx, the DA group underwent continuous reduction in luminal volume (P = 0.022). These changes resulted in a higher incidence of angiographic CAV at 3 years post-HTx in the DA group (58.8% vs 5.6%, P = 0.002). CONCLUSIONS: This volumetric IVUS study suggests that DA correlates with the worsening change in CAV several years post-HTx. Donor-transmitted atherosclerosis recipients may require more aggressive treatment to prevent subsequent CAV progression. Lippincott Williams & Wilkins 2017-06 2016-07-28 /pmc/articles/PMC5441888/ /pubmed/27472091 http://dx.doi.org/10.1097/TP.0000000000001322 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Clinical Science—General: Outcomes Watanabe, Takuya Seguchi, Osamu Yanase, Masanobu Fujita, Tomoyuki Murata, Yoshihiro Sato, Takuma Sunami, Haruki Nakajima, Seiko Kataoka, Yu Nishimura, Kunihiro Hisamatsu, Eriko Kuroda, Kensuke Okada, Norihiro Hori, Yumiko Wada, Kyoichi Hata, Hiroki Ishibashi-Ueda, Hatsue Miyamoto, Yoshihiro Fukushima, Norihide Kobayashi, Junjiro Nakatani, Takeshi Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title | Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title_full | Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title_fullStr | Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title_full_unstemmed | Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title_short | Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis |
title_sort | donor-transmitted atherosclerosis associated with worsening cardiac allograft vasculopathy after heart transplantation: serial volumetric intravascular ultrasound analysis |
topic | Original Clinical Science—General: Outcomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441888/ https://www.ncbi.nlm.nih.gov/pubmed/27472091 http://dx.doi.org/10.1097/TP.0000000000001322 |
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