Division of Cardiothoracic Surgery, Barnes-Jewish Hospital, Washington University School of Medicine, St Louis, Missouri.
Division of Cardiothoracic Surgery, Barnes-Jewish Hospital, Washington University School of Medicine, St Louis, Missouri.
Ann Thorac Surg. 2021 May;111(5):1593-1600. doi: 10.1016/j.athoracsur.2020.07.011. Epub 2020 Sep 16.
Postoperative atrial fibrillation (POAF) is the most common complication after cardiac surgery, and is associated with increased morbidity and mortality. Inflammation has been implicated as an etiology of POAF. Mitochondrial DNA (mtDNA) has been shown to initiate inflammation. This study analyzed inflammatory mechanisms of POAF by evaluating mtDNA, neutrophils, and cytokines/chemokines in the pericardial fluid and blood after cardiac surgery.
Blood and pericardial fluid from patients who underwent coronary artery bypass or heart valve surgery, or both, were collected intraoperatively and at 4, 12, 24, and 48 hours postoperatively. Real-time polymerase chain reaction was used to quantify mtDNA in the pericardial fluid and blood. A Luminex (Luminex Corp, Austin, TX) assay was used to study cytokine and chemokine levels. Flow cytometry was used to analyze neutrophil infiltration and activation in the pericardial fluid.
Samples from 100 patients were available for analysis. Postoperatively, mtDNA and multiple cytokine levels were higher in the pericardial fluid versus blood. Patients who had POAF had significantly higher levels of mtDNA in the pericardial fluid compared with patients who did not (P < .001, area under the curve 0.74). There was no difference in the mtDNA concentration in the blood between the POAF group and non-POAF group (P = .897). Neutrophil concentration increased in the pericardial fluid over time from a baseline of 0.8% to 56% at 48 hours (P < .01).
The pericardial space has a high concentration of inflammatory mediators postoperatively. Mitochondrial DNA in the pericardial fluid was strongly associated with the development of POAF. This finding provides insight into a possible mechanism of inflammation that may contribute to POAF, and may offer novel therapeutic targets.
术后心房颤动(POAF)是心脏手术后最常见的并发症,与发病率和死亡率增加有关。炎症已被认为是 POAF 的病因之一。线粒体 DNA(mtDNA)已被证明可以引发炎症。本研究通过评估心脏手术后心包液和血液中的 mtDNA、中性粒细胞和细胞因子/趋化因子,分析 POAF 的炎症机制。
收集行冠状动脉旁路或心脏瓣膜手术或两者皆行的患者术中及术后 4、12、24 和 48 小时的血液和心包液。实时聚合酶链反应用于定量心包液和血液中的 mtDNA。使用 Luminex(德克萨斯州奥斯汀的 Luminex 公司)检测试剂盒研究细胞因子和趋化因子水平。使用流式细胞术分析心包液中中性粒细胞的浸润和激活。
100 例患者的样本可用于分析。与血液相比,术后心包液中的 mtDNA 和多种细胞因子水平更高。与未发生 POAF 的患者相比,发生 POAF 的患者心包液中的 mtDNA 水平显著升高(P <.001,曲线下面积 0.74)。POAF 组和非 POAF 组之间心包液中的 mtDNA 浓度无差异(P =.897)。中性粒细胞浓度从基线的 0.8%增加到 48 小时时的 56%(P <.01)。
术后心包腔中有高浓度的炎症介质。心包液中的 mtDNA 与 POAF 的发生密切相关。这一发现为炎症的可能机制提供了深入的了解,这可能有助于 POAF,并可能提供新的治疗靶点。