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Leptin, adiponectin, resistin, visfatin serum levels and idiopathic recurrent pericarditis: Biomarkers of disease activity? A preliminary report

机译:瘦素,脂联素,抵抗素,血清血清水平和特发性复发性心包炎:疾病活动的生物标志物? 初步报告

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Objectives Idiopathic recurrent acute pericarditis (IRAP) represents the most troublesome complication of acute pericarditis and is an autoimmune process. White adipose tissue produces more than 50 adipokines that participate in inflammation and autoimmunity. This study investigated whether serum leptin, resistin, visfatin and adiponectin are increased in IRAP versus healthy controls and if their levels correlate with parameters of disease activity. Methods Serum leptin, resistin, visfatin and adiponectin levels were assayed by enzyme-linked immunosorbent assay in 14 IRAP patients during recurrences (group 1), in 23 IRAP patients during symptom-free intervals (group 2) and in 18 healthy controls (group 3). Assessment parameters included demographic characteristics of patients and controls, clinical characteristics of patients and markers of inflammation. Comparisons between groups as well as reciprocal comparisons were evaluated. Results Group 1 showed serum leptin (p0.008), visfatin (p0.002), and adiponectin (p0.04) significantly higher than group 2 and control group, whereas resistin serum levels did not significantly differ (p=0.69). Among IRAP patients, serum leptin significantly correlated with serum amyloid A (SAA) levels (rs=0.43, r2= 0.27, p0.02). Other than this correlation, none of the considered adipokines significantly correlated with the other considered variables in univariate analysis Conclusion Leptin, adiponectin and visfatin are increased in IRAP patients versus healthy controls. Our data suggest that these adipokines might be involved in IRAP pathogenesis and that a possible increased cardiovascular risk in these patients, through an early onset atherosclerosis, should be kept in mind. SAA might be a link between IRAP and increased cardiovascular diseases.
机译:目的特发性复发性急性心膜膜炎(IRAP)代表急性心包炎最麻醉的并发症,是一种自身免疫过程。白色脂肪组织产生超过50个adipokines,参与炎症和自身免疫。本研究研究了IRAP与健康对照中的血清瘦素,抵抗素,缺失和脂肪蛋白,以及它们的水平与疾病活动参数相关。方法通过酶联免疫吸附试验在14例IRAP患者中测定血清瘦素,抵抗素,缺失和脂联素水平,在23例IRAP患者中,在无症状间隔(第2组)和18次健康对照中(第3组) )。评估参数包括患者的人口统计特征和对照,患者的临床特征和炎症标记。评估了组之间的比较以及互惠比较。结果组1显示血清瘦素(P <0.008),粘霉素(P <0.002),脂联素(P <0.04)显着高于第2组和对照组,而抗蛋白血清水平没有显着不同(P = 0.69)。在IRAP患者中,血清瘦素与血清淀粉样蛋白A(SAA)水平显着相关(Rs = 0.43,R2 = 0.27,P <0.02)。除此之外,IRAP患者与健康对照中的其他相关性与单变量分析结论瘦素,脂联素和酵母中的其他变量显着相关。我们的数据表明,这些adipokines可能参与IRAP发病机制,并且通过早期发作的动脉粥样硬化,这些患者的心血管风险可能增加,应牢记。 Saa可能是IRAP和心血管疾病增加的联系。

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