Donor-Transmitted Atherosclerosis Associated With Worsening Cardiac Allograft Vasculopathy After Heart Transplantation: Serial Volumetric Intravascular Ultrasound Analysis

被引:31
作者
Watanabe, Takuya [1 ,2 ]
Seguchi, Osamu [1 ]
Yanase, Masanobu [1 ]
Fujita, Tomoyuki [3 ]
Murata, Yoshihiro [1 ,4 ]
Sato, Takuma [1 ]
Sunami, Haruki [1 ]
Nakajima, Seiko [1 ]
Kataoka, Yu [5 ]
Nishimura, Kunihiro [6 ]
Hisamatsu, Eriko [1 ]
Kuroda, Kensuke [1 ]
Okada, Norihiro [1 ]
Hori, Yumiko [7 ]
Wada, Kyoichi [8 ]
Hata, Hiroki [4 ]
Ishibashi-Ueda, Hatsue [9 ]
Miyamoto, Yoshihiro [2 ]
Fukushima, Norihide [1 ]
Kobayashi, Junjiro [4 ]
Nakatani, Takeshi [1 ]
机构
[1] Natl Cerebral & Cardiovasc Ctr, Dept Transplantat, 5-7-1 Fujishiro Dai, Suita, Osaka 5658565, Japan
[2] Natl Cerebral & Cardiovasc Ctr, Dept Prevent Cardiol, Suita, Osaka, Japan
[3] Natl Cerebral & Cardiovasc Ctr, Dept Cardiovasc Surg, Suita, Osaka, Japan
[4] Kumiai Kosei Hosp, Dept Cardiol, Takayama, Gifu, Japan
[5] Natl Cerebral & Cardiovasc Ctr, Dept Cardiovasc Med, Suita, Osaka, Japan
[6] Natl Cerebral & Cardiovasc Ctr, Dept Prevent Med & Epidemiol Informat, Suita, Osaka, Japan
[7] Natl Cerebral & Cardiovasc Ctr, Dept Nursing, Suita, Osaka, Japan
[8] Natl Cerebral & Cardiovasc Ctr, Dept Pharm, Suita, Osaka, Japan
[9] Natl Cerebral & Cardiovasc Ctr, Dept Pathol, Suita, Osaka, Japan
关键词
CORONARY-ARTERY-DISEASE; MYCOPHENOLATE-MOFETIL; INTERNATIONAL SOCIETY; WORKING FORMULATION; MULTICENTER TRIAL; PROGRESSION; RECIPIENTS; EVEROLIMUS; OUTCOMES; NOMENCLATURE;
D O I
10.1097/TP.0000000000001322
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1310 / 1319
页数:10
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