Pugliese Nicola R, Fabiani Iacopo, Conte Lorenzo, Nesti Lorenzo, Masi Stefano, Natali Andrea, Colombo Paolo C, Pedrinelli Roberto, Dini Frank L
Cardiac, Thoracic and Vascular Department, University of Pisa, Pisa.
Department of Clinical and Experimental Medicine, University of Pisa, Pisa.
J Cardiovasc Med (Hagerstown). 2020 Jul;21(7):494-502. doi: 10.2459/JCM.0000000000000974.
Chronic kidney dysfunction (CKD) and persistent congestion influence heart failure prognosis, but little is known about the role of inflammation in this association. We assessed the relationship between inflammatory biomarkers, persistent congestion and CKD and their prognostic implications in patients with acute heart failure.
We enrolled 97 hospitalised patients (mean age: 66 ± 12 years, ejection fraction: 30 ± 8%) with acute heart failure. Before discharge, congestion was assessed using a heart failure scoring system on the basis of Framingham criteria. Circulating levels of high-sensitivity C-reactive protein, TGF-β-1, IL-1, IL-6, IL-10, TNF-α, soluble tumour necrosis factor receptor type 1 and 2 were measured. Patients were divided into four groups according to the presence of CKD (estimated glomerular filtration rate <60 ml/min/1.73 m) and congestion (Framingham heart failure score ≥2). The primary end point was the combination of death and rehospitalisation for acute heart failure.
During a median follow-up of 32 months, 37 patients died and 14 were rehospitalised for acute heart failure. Patients with CKD and congestion had significantly higher TNF-α (P = 0.037), soluble tumour necrosis factor receptor type 1 (P = 0.0042) and soluble tumour necrosis factor receptor type 2 (P = 0.001), lower TGF-β-1 (P = 0.02) levels, and the worst outcome (P < 0.0001). Congestion (P = 0.01) and CKD (P = 0.02) were independent predictors of the end-point together with N-terminal prohormone of brain natriuretic peptide (P = 0.002) and TNF-α (P = 0.004). TNF-α attenuated the direct relation between CKD, congestion and outcome, explaining 40% of the difference in the outcome.
In patients hospitalised with acute heart failure, the prognostic impact of persistent congestion and CKD is associated with increased cytokine levels, which may also interfere with the outcome.
慢性肾功能不全(CKD)和持续性充血影响心力衰竭的预后,但关于炎症在此关联中的作用知之甚少。我们评估了炎症生物标志物、持续性充血和CKD之间的关系及其对急性心力衰竭患者的预后影响。
我们纳入了97例因急性心力衰竭住院的患者(平均年龄:66±12岁,射血分数:30±8%)。出院前,根据弗雷明汉标准使用心力衰竭评分系统评估充血情况。测量高敏C反应蛋白、转化生长因子-β1、白细胞介素-1、白细胞介素-6、白细胞介素-10、肿瘤坏死因子-α、可溶性肿瘤坏死因子受体1型和2型的循环水平。根据CKD(估计肾小球滤过率<60ml/min/1.73m²)和充血(弗雷明汉心力衰竭评分≥2)的情况将患者分为四组。主要终点是死亡和因急性心力衰竭再次住院的联合情况。
在中位随访32个月期间,37例患者死亡,14例因急性心力衰竭再次住院。患有CKD和充血的患者肿瘤坏死因子-α(P=0.037)、可溶性肿瘤坏死因子受体1型(P=0.0042)和可溶性肿瘤坏死因子受体2型(P=0.001)水平显著更高,转化生长因子-β1水平更低(P=0.02),且预后最差(P<0.0001)。充血(P=0.01)、CKD(P=0.02)与脑钠肽N末端前体激素(P=0.002)和肿瘤坏死因子-α(P=0.004)一起是终点的独立预测因素。肿瘤坏死因子-α减弱了CKD、充血与预后之间的直接关系,解释了预后差异的40%。
在因急性心力衰竭住院的患者中,持续性充血和CKD的预后影响与细胞因子水平升高有关,这也可能干扰预后。