医学
心包炎
干燥综合征
疾病
全身性疾病
背景(考古学)
全身炎症
免疫学
自身抗体
皮肤病科
炎症
内科学
抗体
生物
古生物学
作者
Κωνσταντίνος Μελισσαρόπουλος,Dimitrios P. Bogdanos,Theodoros Dimitroulas,Lazaros I. Sakkas,George D. Kitas,Dimitrios Daoussis
出处
期刊:Current Vascular Pharmacology
[Bentham Science]
日期:2020-08-10
卷期号:18 (5): 447-454
被引量:28
标识
DOI:10.2174/1570161118666200129125320
摘要
Sjögren’s syndrome is a rheumatic autoimmune disease that primarily affects middle-aged women and runs a slowly progressing course with sicca symptoms being the prevalent manifestation. Premature atherosclerosis and increased cardiovascular (CV) morbidity and mortality are frequently encountered in rheumatic diseases characterized by significant systemic inflammation, such as the inflammatory arthritides, systemic vasculitides and systemic lupus erythematosus. In the same context, chronic inflammation and immune aberrations underlying Sjögren’s syndrome are also reported to be associated with augmented risk of atherosclerosis. Increased CV disease (CVD) frequency has been found in recent meta-analyses. The involvement of the CV system is not a common feature of Sjögren’s syndrome; however, specific manifestations, such as autoantibody-mediated heart block, pericarditis, pulmonary arterial hypertension and dysautonomia, have been described. This review focuses on studies addressing CV morbidity in Sjögren’s syndrome and presents current data regarding distinct CV features of the disease.
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