Literature DB >> 30172475

Clinical and imaging manifestations of Takayasu's arteritis with pulmonary hypertension: A retrospective cohort study in China.

Juanni Gong1, Yuanhua Yang2, Zhanhong Ma3, Xiaojuan Guo3, Jianfeng Wang4, Tuguang Kuang1, Suqiao Yang1, Jifeng Li1, Ran Miao5, Kewu Huang6.   

Abstract

BACKGROUND: Takayasu's arteritis with pulmonary artery involvement (PTA) is uncommon and part of which may be accompanied by pulmonary hypertension (PH). This study herein investigated the clinical presentation, imaging features, and outcomes in PTA patients with and without PH.
METHODS: A total of 57 PTA patients were selected at the Beijing Chao-Yang Hospital from January 2011 to July 2017. Patients were placed into two groups, PTA-with-PH or PTA-without-PH. The clinical characteristics, imaging features, and outcomes of patients in these two groups were investigated.
RESULTS: Among the 57 PTA patients, 24 were in the PTA-without-PH group and 33 were in the PTA-with-PH group. The disease duration in PTA-with-PH patients was longer than that of PTA-without-PH patients. The mean follow-up duration of 43 patients was 33.5 ± 20.3 months, while three patients in the PTA-with-PH were deceased. The PTA-with-PH group had significantly higher prevalence of chest tightness and dyspnea, shorter 6-minute walk distance (6MWD) and higher Borg scores after walk than that the PTA-without-PH group. Imaging analyses revealed that patients had five different arterial lesions (stenosis, occlusion, vascular wall thickening, in situ thrombosis, and aneurysm), but aneurysms were only detected in patients in PTA-with-PH patients at 42%. Compared with PTA-without-PH patients, PTA-with-PH patients tended to have occlusion lesions, but less likely to have vascular wall thickening.
CONCLUSIONS: Compared with PTA-without-PH patients, PTA-with-PH patients had longer disease duration, more severe symptoms and tended to be deceased during the follow-up time. In addition, PTA-with-PH patients tended to have aneurysm and occlusion vessel lesions.
Copyright © 2018. Published by Elsevier B.V.

Entities:  

Keywords:  Aneurysm; Pulmonary hypertension; Pulmonary vascular disease; Takayasu's arteritis

Mesh:

Year:  2018        PMID: 30172475     DOI: 10.1016/j.ijcard.2018.08.047

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  4 in total

Review 1.  Imaging of Chronic Thromboembolic Disease.

Authors:  Adina Haramati; Linda B Haramati
Journal:  Lung       Date:  2020-03-12       Impact factor: 2.584

Review 2.  Successful Early Immunosuppressive Therapy for Pulmonary Arterial Hypertension Due to Takayasu arteritis: Two Case Reports and a Review of Similar Case Reports in the English Literature.

Authors:  Takuya Suda; Takeshi Zoshima; Kiyoaki Ito; Ichiro Mizushima; Mitsuhiro Kawano
Journal:  Intern Med       Date:  2021-11-13       Impact factor: 1.282

3.  Involvement of the pulmonary arteries in patients with Takayasu arteritis: a prospective study from a single centre in China.

Authors:  Xiufang Kong; Lili Ma; Peng Lv; Xiaomeng Cui; Rongyi Chen; Zongfei Ji; Huiyong Chen; Jiang Lin; Lindi Jiang
Journal:  Arthritis Res Ther       Date:  2020-06-05       Impact factor: 5.156

4.  The clinical features of pulmonary artery involvement in Takayasu arteritis and its relationship with ischemic heart diseases and infection.

Authors:  Hiroki Mukoyama; Mirei Shirakashi; Nozomi Tanaka; Takeshi Iwasaki; Toshiki Nakajima; Hideo Onizawa; Hideaki Tsuji; Koji Kitagori; Shuji Akizuki; Ran Nakashima; Kosaku Murakami; Masao Tanaka; Akio Morinobu; Hajime Yoshifuji
Journal:  Arthritis Res Ther       Date:  2021-12-03       Impact factor: 5.156

  4 in total

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