Suppr超能文献

大动脉炎中肺动脉受累情况:一项针对中国人群的回顾性研究

Pulmonary artery involvement in Takayasu arteritis: a retrospective study in Chinese population.

作者信息

Xi Xin, Du Juan, Liu Jiayi, Zhu Guangfa, Qi Guanming, Pan Lili

机构信息

Sleep Center, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

Department of Pulmonary and Critical Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

出版信息

Clin Rheumatol. 2021 Feb;40(2):635-644. doi: 10.1007/s10067-020-05271-5. Epub 2020 Jul 8.

Abstract

BACKGROUND

Takayasu's arteritis (TA) may involve the pulmonary artery, which signifies a poor prognosis. This study investigated the features of TA patients with pulmonary artery involvement.

METHODS

One hundred and twenty-six inpatients diagnosed with TA were retrospectively studied. The clinical data of TA patients with and without pulmonary artery involvement were compared. The imaging features of pulmonary artery lesions in TA patients were evaluated. The treatment responses of pulmonary artery lesions were described, and the drug regimens in different treatment response groups were compared.

RESULTS

Among the patients with TA, 15.9% showed associated pulmonary artery involvement. The disease durations were significantly longer in patients with pulmonary artery involvement than in those without (108.0 months (53.5, 222.0) vs. 36.0 months (12.0, 120.0); p = 0.038). Hemoptysis was more common in TA patients with pulmonary artery involvement than in those without (15.0%, 3 cases vs. 0.0%; p < 0.001). TA patients with disease duration longer than 5 years showed a 3.42-fold higher odds of pulmonary artery involvement than those with a disease duration of less than 5 years (adjusted odds ratio, 3.42 (95% confidence interval, 1.20-9.76); p = 0.02). The most common imaging manifestations of pulmonary artery involvement were stenosis and occlusion. Among the six patients who had good response to treatment of pulmonary artery lesions, five were treated with the interleukin-6 receptor antagonist tocilizumab.

CONCLUSIONS

TA patients with pulmonary artery involvement have a longer course of disease and more symptoms of hemoptysis. TA-related pulmonary artery lesions more commonly manifested as stenosis and occlusion. Tocilizumab may be effective for TA-related pulmonary vascular disease. Key Points • Disease duration longer than 5 years is associated with pulmonary artery involvement in TA. • Hemoptysis is a characteristic clinical symptom of TA with pulmonary artery involvement. • Tocilizumab may be more effective for pulmonary artery lesions of TA.

摘要

背景

大动脉炎(TA)可能累及肺动脉,这预示着预后不良。本研究调查了合并肺动脉受累的TA患者的特征。

方法

对126例诊断为TA的住院患者进行回顾性研究。比较了合并和未合并肺动脉受累的TA患者的临床资料。评估了TA患者肺动脉病变的影像学特征。描述了肺动脉病变的治疗反应,并比较了不同治疗反应组的药物治疗方案。

结果

在TA患者中,15.9%表现为合并肺动脉受累。合并肺动脉受累患者的病程明显长于未合并者(108.0个月(53.5,222.0)对36.0个月(12.0,120.0);p = 0.038)。合并肺动脉受累的TA患者咯血比未合并者更常见(15.0%,3例对0.0%;p < 0.001)。病程超过5年的TA患者合并肺动脉受累的几率比病程小于5年的患者高3.42倍(调整后的优势比,3.42(95%置信区间,1.20 - 9.76);p = 0.02)。肺动脉受累最常见的影像学表现为狭窄和闭塞。在6例肺动脉病变治疗反应良好的患者中,5例接受了白细胞介素-6受体拮抗剂托珠单抗治疗。

结论

合并肺动脉受累的TA患者病程更长,咯血症状更多。TA相关的肺动脉病变更常见的表现为狭窄和闭塞。托珠单抗可能对TA相关的肺血管疾病有效。要点 • 病程超过5年与TA患者的肺动脉受累有关。 • 咯血是TA合并肺动脉受累的特征性临床症状。 • 托珠单抗可能对TA的肺动脉病变更有效。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验