Mascolo Ruggiero, Bizzi Emanuele, Martelli Martina, Facoetti Chiara, Colazzo Giulia, Barone Fabio, Brucato Antonio
Division of Internal Medicine, Fatebenefratelli Hospital, ASST Fatebenefratelli Sacco, University of Milan, Piazzale Principessa Clotilde, 3, Milan, 20121, Italy.
Department of Biomedical and Clinical Sciences, University of Milan, Via G.B. Grassi, 74, Milan, 20157, Italy.
Curr Cardiol Rep. 2025 Jan 11;27(1):17. doi: 10.1007/s11886-024-02170-y.
To outline the latest discoveries regarding the utility and reliability of serum biomarkers in idiopathic recurrent acute pericarditis (IRAP), considering recent findings on its pathogenesis. The study highlights the predictive role of these biomarkers in potential short- (cardiac tamponade, recurrences) and long-term complications (constrictive pericarditis, death).
The pathogenesis of pericarditis has been better defined in recent years, focusing on the autoinflammatory pathway. New studies have demonstrated the pivotal role of the classical inflammatory biomarkers in distinguishing pericarditis phenotypes (high-grade vs. low-grade inflammation) and in defining outcomes of this condition. Pericarditis involves intense inflammatory activity, which causes elevation of different markers, such as C-reactive protein, erythrocyte sedimentation rate, neutrophils and platelets, serum amyloid A and D-Dimer. Conversely, lymphocytes are often reduced, as well as hemoglobin during the acute phase. Cardiac troponins T and I are elevated in up to 30% of cases. A Biomarker for CRP-negative cases is needed. Other markers have been proposed for diagnosis and prognosis in IRAP, such as anti-heart antibodies and anti-intercalated disk antibodies, but we need further studies to validate them.
鉴于特发性复发性急性心包炎(IRAP)发病机制的最新研究结果,概述血清生物标志物在IRAP中的效用和可靠性的最新发现。本研究强调了这些生物标志物在潜在短期(心脏压塞、复发)和长期并发症(缩窄性心包炎、死亡)中的预测作用。
近年来,心包炎的发病机制已得到更明确的定义,重点在于自身炎症途径。新的研究表明,经典炎症生物标志物在区分心包炎表型(高度炎症与低度炎症)以及确定该病的预后方面具有关键作用。心包炎涉及强烈的炎症活动,这会导致不同标志物升高,如C反应蛋白、红细胞沉降率、中性粒细胞和血小板、血清淀粉样蛋白A和D-二聚体。相反,淋巴细胞通常会减少,急性期血红蛋白也会降低。高达30%的病例中心肌肌钙蛋白T和I会升高。需要一种针对C反应蛋白阴性病例的生物标志物。已提出其他标志物用于IRAP的诊断和预后评估,如抗心脏抗体和抗闰盘抗体,但我们需要进一步研究来验证它们。