Effect of levosimendan combined with lyophilised recombinant human brain natriuretic peptide on ventricular remodelling in patients with ischemic cardiomyopathy
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摘要:
目的 观察左西孟旦联合冻干重组人脑利钠肽治疗缺血性心肌病的临床疗效及对心功能损伤和心室重构的改善作用。 方法 选择2018年6月—2021年2月宁波市第四医院心内科收治的240例缺血性心肌病心力衰竭患者为研究对象,按照随机数字表法分为对照组(120例)和研究组(120例)。对照组患者予以常规治疗,研究组患者增加左西孟旦联合冻干重组人脑利钠肽治疗。检测2组患者治疗前后血清转化生长因子β1(TGF-β1)、核因子-κB(NF-κB)、成纤维细胞生长因23(FGF23)、胱抑素C(CysC)、肌酸激酶同工酶(CK-MB)、N末端原脑利钠肽(NT-proBNP)和超敏C反应蛋白(hs-CRP)等血清生化指标水平,统计左心室舒张末期内径(LVEDD)、左心室收缩末期内径(LVESD)、左室收缩末期容积(LVEDV)、左室收缩末期容积(LVESV)及左心室射血分数(LVEF)等心脏超声指标变化,评价患者治疗后临床疗效,进行6分钟步行试验,观察治疗期间药物不良反应。 结果 治疗后,研究组患者血清NF-κB、CysC、CK-MB、NT-proBNP和hs-CRP含量均显著低于对照组(均P < 0.05);研究组LVEDV和LVESV均显著低于对照组(均P < 0.05),而LVEF[(54.18±4.94)%]显著高于对照组[(49.62±4.61)%, P < 0.05];研究组治疗总体有效率为90.83%,显著高于对照组(76.67%,P < 0.05);研究组治疗后6分钟步行试验结果为(436.51±33.82)m,对照组为(392.74±28.61)m,2组比较差异有统计学意义(P < 0.05)。2组均未出现药物不良反应。 结论 给予缺血性心肌病心力衰竭患者左西孟旦及冻干重组人脑利钠肽联合用药治疗,可有效减轻心室重构和心肌损伤程度,增强心肌功能,提高疗效水平,安全性高。 Abstract:Objective To observe the clinical efficacy of levosimendan combined with lyophilised recombinant human brain natriuretic peptide (neoactivin) in the treatment of ischemic cardiomyopathy and the improvement of cardiac function damage and ventricular remodelling. Methods A total of 240 patients with ischemic cardiomyopathy heart failure admitted to the Department of Cardiology in Ningbo Fourth Hospital from June 2018 to February 2021 were selected as the research objects. The patients were randomly divided into the control group (120 cases) and study group (120 cases) according to the random number table method. The patients in the control group were given conventional treatment, whilst those in the study group were treated with levosimendan combined with neoactivin. The serum levels of TGF-β1, NF-κB, FGF23, CysC, CK-MB, NT-proBNP and hs-CRP in both groups before and after treatment were detected. The changes in LVEDD, LVESD, LVEDV, LVESV and LVEF were statistically analysed. The clinical efficacy of heart failure after treatment was evaluated. The 6-min walk test was conducted. The incidence of adverse drug reactions during treatment was observed. Results After treatment, serum levels of NF-κB, CysC, CK-MB, NT-proBNP and hs-CRP in the study group were significantly lower than those in the control group (all P < 0.05). The detection values of LVEDV and LVESV in the study group were significantly lower than those in the control group, whilst LVEF (54.18±4.94) % was significantly higher than that in the control group (49.62±4.61) % (all P < 0.05). The total effective rate of the study group (90.83%) was significantly higher than that of the control group (76.67%, P < 0.05). The results of the 6-min walk test in the study group [(436.51±33.82) m] was significantly better than that in the control group [(392.74±28.61) m, P < 0.05]. No adverse drug reactions were observed in both groups during treatment. Conclusion Levosimendan combined with neoactivin can effectively alleviate ventricular remodelling, inhibit myocardial injury, improve myocardial function, improve the level of curative effect and has high safety. -
表 1 2组缺血性心肌病心力衰竭患者治疗前后血清生化指标比较
(x ±s) 组别 例数 TGF-β1(ng/mL) NF-κB(pg/mL) FGF23(pg/mL) CysC(μg/mL) 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 对照组 120 52.37±6.51 41.16±5.74a 80.52±9.41 54.46±6.13a 671.09±78.73 487.23±49.26a 2.98±0.37 1.87±0.24a 研究组 120 53.49±6.74 39.93±5.17a 81.67±9.72 48.74±5.63a 682.42±71.42 479.64±42.53a 3.04±0.35 1.24±0.19a t值 1.314 1.745 0.931 7.577 1.167 1.318 1.341 22.241 P值 0.190 0.082 0.353 <0.001 0.224 0.189 0.181 <0.001 组别 例数 CK-MB(U/L) NT-proBNP(pg/mL) hs-CRP(μg/mL) 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 对照组 120 158.62±16.53 74.62±6.31a 3 516.45±259.62 2 064.74±141.63a 6.82±0.79 2.93±0.31a 研究组 120 157.41±16.21 65.86±5.93a 3 530.27±263.35 1 498.39±126.37a 6.75±0.74 2.65±0.27a t值 0.575 11.081 0.410 32.653 0.711 7.361 P值 0.566 <0.001 0.682 <0.001 0.478 <0.001 注:与治疗前比较,aP<0.001。TGF-β1为血清转化生长因子β1,NF-κB为核因子-κB,FGF23为成纤维细胞生长因23,CysC为胱抑素C,CK-MB为肌酸激酶同工酶,NT-proBNP为N末端原脑利钠肽,hs-CRP为超敏C反应蛋白。 表 2 2组缺血性心肌病心力衰竭患者治疗前后心脏超声指标比较
(x ±s) 组别 例数 LVEDD(mm) LVESD(mm) LVEDV(mL) LVESV(mL) LVEF(%) 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 治疗前 治疗后 对照组 120 66.52±5.63 53.19±4.96a 45.63±6.63 38.25±4.49a 117.69±12.84 98.62±8.47a 63.84±7.26 49.59±5.47a 38.93±3.67 49.62±4.61a 研究组 120 65.93±5.83 52.64±4.83a 44.29±6.84 37.41±4.27a 118.27±12.23 91.48±7.83a 64.45±7.51 44.63±5.21a 39.07±3.56 54.18±4.94a t值 0.793 0.870 1.542 1.485 0.363 6.779 0.645 7.192 0.300 7.388 P值 0.428 0.385 0.124 0.139 0.717 <0.001 0.519 <0.001 0.765 <0.001 注:与治疗前比较,aP<0.001。LVEDD为左心室舒张末期内径,LVESD为左心室收缩末期内径,LVEDV为左室收缩末期容积,LVESV为左室收缩末期容积,LVEF为左心室射血分数。 表 3 2组缺血性心肌病心力衰竭患者临床总有效率比较
[例(%)] 组别 例数 显效 有效 无效 总有效 对照组 120 25(20.83) 67(55.83) 28(23.33) 92(76.67) 研究组 120 45(37.50) 64(53.33) 11(9.17) 109(90.83) 注:2组总有效率比较,χ2=8.848,P=0.003。 -
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