Hwang Hyeon Seok, Kim Jin Sug, Kim Yang Gyun, Lee Yu Ho, Lee Dong-Young, Ahn Shin Young, Moon Ju-Young, Lee Sang-Ho, Ko Gang-Jee, Jeong Kyung Hwan
Division of Nephrology, Department of Internal Medicine, KyungHee University, Seoul, South Korea.
Division of Nephrology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
Front Cardiovasc Med. 2021 Jun 15;8:684297. doi: 10.3389/fcvm.2021.684297. eCollection 2021.
Neprilysin inhibition has demonstrated impressive benefits in heart failure treatment, and is the current focus of interest in cardiovascular (CV) and kidney diseases. However, the role of circulating neprilysin as a biomarker for CV events is unclear in hemodialysis (HD) patients. A total of 439 HD patients from the K-cohort were enrolled from June 2016 to April 2019. The plasma neprilysin level and echocardiographic findings at baseline were examined. The patients were prospectively followed up to assess the primary endpoint (composite of CV events and cardiac events). Plasma neprilysin level was positively correlated with left ventricular (LV) mass index, LV end-systolic volume, and LV end-diastolic volume. Multivariate linear regression analysis revealed that neprilysin level was negatively correlated with LV ejection fraction (β = -2.14; = 0.013). The cumulative event rate of the composite of CV events was significantly greater in neprilysin tertile 3 ( = 0.049). Neprilysin tertile 3 was also associated with an increased cumulative event rate of cardiac events ( = 0.016). In Cox regression analysis, neprilysin tertile 3 was associated with a 2.61-fold risk for the composite of CV events [95% confidence interval (CI), 1.37-4.97] and a 2.72-fold risk for cardiac events (95% CI, 1.33-5.56) after adjustment for multiple variables. Higher circulating neprilysin levels independently predicted the composite of CV events and cardiac events in HD patients. The results of this study suggest the importance of future studies on the effect of neprilysin inhibition in reducing CV events.
中性肽链内切酶抑制在心力衰竭治疗中已显示出显著益处,并且是当前心血管(CV)疾病和肾脏疾病研究的热点。然而,在血液透析(HD)患者中,循环中性肽链内切酶作为CV事件生物标志物的作用尚不清楚。2016年6月至2019年4月,共纳入了K队列的439例HD患者。检测了基线时的血浆中性肽链内切酶水平和超声心动图结果。对患者进行前瞻性随访,以评估主要终点(CV事件和心脏事件的复合终点)。血浆中性肽链内切酶水平与左心室(LV)质量指数、LV收缩末期容积和LV舒张末期容积呈正相关。多变量线性回归分析显示,中性肽链内切酶水平与LV射血分数呈负相关(β = -2.14;P = 0.013)。在中性肽链内切酶三分位数3组中,CV事件复合终点的累积事件发生率显著更高(P = 0.049)。中性肽链内切酶三分位数3组也与心脏事件的累积事件发生率增加相关(P = 0.016)。在Cox回归分析中,经多变量调整后,中性肽链内切酶三分位数3组发生CV事件复合终点的风险增加2.61倍[95%置信区间(CI),1.37 - 4.97],发生心脏事件的风险增加2.72倍(95%CI,1.33 - 5.56)。较高的循环中性肽链内切酶水平可独立预测HD患者的CV事件和心脏事件复合终点。本研究结果提示了未来研究中性肽链内切酶抑制对减少CV事件影响的重要性。