Xie Xiaohui, Chen Jiahong, Yu Lei, Sun Jianzhong, Zhao Chengchen, Duan Qingqing
Department of Nephrology, Zhejiang Hospital, 310009 Hangzhou, Zhejiang, China.
Department of Nephrology, Xiamen Hongai Hospital, 361000 Xiamen, Fujian, China.
Rev Cardiovasc Med. 2024 Apr 22;25(4):148. doi: 10.31083/j.rcm2504148. eCollection 2024 Apr.
Inflammation is essential in cardiorenal syndrome, however there is still a lack of evidence proving the interaction between cardiac injury, renal dysfunction and the inflammatory response. This study aimed to illustrate the association between renal dysfunction and cardiac injury with a specific focus on the role of inflammation.
A single-center, retrospective study included patients with heart failure admitted to the cardiovascular department from September 2019 to April 2022. Patients received cardiovascular magnetic resonance (CMR) imaging (T1 mapping and late gadolinium enhancement (LGE)). Demographic, creatinine and native T1 were analyzed using pearson correlation, linear regression and adjusted for confounders. Interaction and subgroup analysis were performed.
Finally, 50 validated heart failure (HF) patients (age 58.5 14.8 years; 78.0% men) were included. Cardiac global native T1 for the high estimated glomeruar filtration rate (eGFR) group was 1117.0 56.6 ms, and for the low eGFR group was 1096.5 61.8 ms. Univariate analysis identified global native T1 ( = 0.16, 95% confidence interval (CI): 0.04-0.28, = 0.014) and C-reactive protein (CRP) ( = 0.30, 95% CI: 0.15-0.45, 0.001) as determinants of creatinine. Multivariable linear regression analysis identified global native T1 ( = 0.12, 95% CI: 0.01-0.123, = 0.040) as a determinant of creatinine while age and diabetes were adjusted. Significant interactions between CRP and global native T1 in relation to creatinine level ( for interaction = 0.005) were identified.
Kidney dysfunction was associated with cardiac injury and inflammation, respectively. The interaction between myocardial injury and kidney dysfunction is contingent on the severity of the inflammatory response. Further studies were needed to identify the mechanisms of the inflammatory response in cardiorenal syndrome.
炎症在心肾综合征中至关重要,然而,仍缺乏证据证明心脏损伤、肾功能不全与炎症反应之间的相互作用。本研究旨在阐明肾功能不全与心脏损伤之间的关联,并特别关注炎症的作用。
一项单中心回顾性研究纳入了2019年9月至2022年4月心血管科收治的心力衰竭患者。患者接受了心血管磁共振(CMR)成像(T1 mapping和延迟钆增强(LGE))。使用Pearson相关性分析、线性回归分析人口统计学、肌酐和固有T1,并对混杂因素进行校正。进行了交互作用和亚组分析。
最终,纳入了50例经证实的心力衰竭(HF)患者(年龄58.5±14.8岁;78.0%为男性)。高估计肾小球滤过率(eGFR)组的心脏整体固有T1为1117.0±56.6毫秒,低eGFR组为1096.5±61.8毫秒。单因素分析确定整体固有T1(β = 0.16,95%置信区间(CI):0.04 - 0.28,P = 0.014)和C反应蛋白(CRP)(β = 0.30,95%CI:0.15 - 0.45,P < 0.001)为肌酐的决定因素。多变量线性回归分析确定整体固有T1(β = 0.12,95%CI:0.01 - 0.123,P = 0.040)为肌酐的决定因素,同时对年龄和糖尿病进行了校正。确定了CRP与整体固有T1之间在肌酐水平方面存在显著交互作用(交互作用的P = 0.005)。
肾功能不全分别与心脏损伤和炎症相关。心肌损伤与肾功能不全之间的相互作用取决于炎症反应的严重程度。需要进一步研究以确定心肾综合征中炎症反应的机制。