Phenotype of Takayasu-like vasculitis and cardiopathy in patients with Blau syndrome

被引:0
|
作者
Zhong, Linqing [1 ]
Wang, Wei [1 ]
Tang, Xiaoyan [1 ]
Zhang, Yu [1 ]
Gou, Lijuan [1 ]
Wang, Lin [1 ]
Wang, Changyan [1 ]
Jian, Shan [1 ]
Quan, Meiying [1 ]
Zhang, Zhenjie [1 ]
Yu, Zhongxun [1 ]
Qiu, Zhengqing [1 ]
Wei, Min [1 ]
Song, Hongmei [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Pediat, Beijing 100730, Peoples R China
关键词
Blau syndrome; Cardiovascular involvement; Large vessel vasculitis; Takayasu arteritis; TERM-FOLLOW-UP; ARTERITIS; MUTATIONS; GRANULOMATOSIS; CLASSIFICATION; INFLIXIMAB; INHIBITORS; CRITERIA;
D O I
10.1007/s10067-024-06876-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives We aimed to determine the prevalence of cardiovascular involvement in our Blau syndrome (BS) cohort and provide detailed analysis of their cardiovascular manifestations and outcome. We also tried to find out the risk factors for developing cardiovascular involvement. Methods Clinical manifestations, laboratory findings, and treatments were reviewed. Clinical features were compared between children with cardiovascular involvement and those without angiocardiopathy. Results A total of 38 BS children were eligible for final analysis. Among them, 13 (34.2%) developed Takayasu-like vasculitis and/or cardiopathy. Compared with those without angiocardiopathy, recurrent fever was more frequent in BS patients with cardiovascular involvement (p < 0.001). What is more, tumor necrosis factor alpha antagonists (anti-TNF) were more urgently needed in children with cardiovascular involvement (p = 0.015). BS patients with cardiovascular involvement include 4 with Takayasu-like vasculitis and 9 with cardiopathy. The onset of cardiovascular manifestations ranged from 0.75 to 18.5 years of age, with most cases occurring before school period. Symptoms were elusive and lacked specificity, such as dizziness, short of breath, and edema. Some patients were even identified because of the unexpected hypertension during follow-up. Cardiopathy and vasculitis occurred in patients with different genotypes. Imaging changes were discovered before the presentation of the typical triad in 3/4 patients with Takayasu-like vasculitis. Three children developed left ventricular dysfunction with decreased left ventricular ejection fraction. Combination of glucocorticoids and methotrexate with anti-TNF agents is a common treatment option for these BS patients. In the cohort, BS-related cardiovascular involvement was controlled well, with cardiac structural and functional abnormalities completely recovered and slower progression of vasculitis lesions. Conclusion Cardiovascular manifestations is not rare in BS patients. Because of its insidious onset, a systematic and comprehensive assessment of cardiovascular involvement should be performed in newly diagnosed patients with BS. Aggressive initiation of anti-TNF agents may be beneficial to improve the prognosis.
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收藏
页码:1171 / 1181
页数:11
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