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达格列净对射血分数轻度下降性心力衰竭患者心脏结构及功能的影响

徐孟丹 向虹 高晓龙 张进 吴海燕 王礼琳

徐孟丹, 向虹, 高晓龙, 张进, 吴海燕, 王礼琳. 达格列净对射血分数轻度下降性心力衰竭患者心脏结构及功能的影响[J]. 昆明医科大学学报, 2024, 45(11): 95-102. doi: 10.12259/j.issn.2095-610X.S20241114
引用本文: 徐孟丹, 向虹, 高晓龙, 张进, 吴海燕, 王礼琳. 达格列净对射血分数轻度下降性心力衰竭患者心脏结构及功能的影响[J]. 昆明医科大学学报, 2024, 45(11): 95-102. doi: 10.12259/j.issn.2095-610X.S20241114
Mengdan XU, Hong XIANG, Xiaolong GAO, Jin ZHANG, Haiyan WU, Lilin WANG. Effect of Dapagliflozin on Cardiac Structure and Function in Patients with Heart Failure Due to Mildly Reduced Ejection Fraction[J]. Journal of Kunming Medical University, 2024, 45(11): 95-102. doi: 10.12259/j.issn.2095-610X.S20241114
Citation: Mengdan XU, Hong XIANG, Xiaolong GAO, Jin ZHANG, Haiyan WU, Lilin WANG. Effect of Dapagliflozin on Cardiac Structure and Function in Patients with Heart Failure Due to Mildly Reduced Ejection Fraction[J]. Journal of Kunming Medical University, 2024, 45(11): 95-102. doi: 10.12259/j.issn.2095-610X.S20241114

达格列净对射血分数轻度下降性心力衰竭患者心脏结构及功能的影响

doi: 10.12259/j.issn.2095-610X.S20241114
基金项目: 国家自然科学基金资助项目(81360039);云南省科技厅-昆明医科大学应用基础研究联合专项基金资助项目(202401AY070001-310)
详细信息
    作者简介:

    徐孟丹(1995~),女,河南周口人,在读硕士研究生,住院医师,主要从事心血管疾病诊疗工作

    通讯作者:

    王礼琳,E-mail:kmwanglin@163.com

  • 中图分类号: R541.6

Effect of Dapagliflozin on Cardiac Structure and Function in Patients with Heart Failure Due to Mildly Reduced Ejection Fraction

  • 摘要:   目的   探讨达格列净对射血分数轻度下降性心力衰竭患者心脏结构及功能的影响。  方法  选取2021年11月1日至2022年12月31日在云南省第一人民医院门诊及住院确诊为射血分数轻度下降性心力衰竭的患者。根据是否服用达格列净将患者分为常规抗心衰组(41例)和达格列净组(44例)。常规抗心衰组进行常规的抗心衰治疗,达格列净组在常规抗心衰治疗(袢利尿剂、ACEI/ARB/ARNI、螺内酯、β受体阻滞剂)的基础上给予口服达格列净。观察2组治疗后3个月、6个月、1 a患者的心功能改善情况、LVEDD(左室舒张末期内径)、LVESD(左室收缩末期内径)、LVEF(左室射血分数)、IVST(室间隔厚度)、LVPWT(左室后壁厚度)、LAD(左房内径)及1 a内不良事件发生率。  结果  达格列净组33例、常规抗心衰组37例完成随访。(1)随访3月、6月、1 a,2组患者的NYNH心功能分级均较治疗前有所改善,达格列净组总有效率显著大于常规抗心衰组(P < 0.05);(2)2组患者LVEF均较基线升高,LVEDD、LVESD、LAD、IVST、LVPWT均较基线下降(P < 0.05);(3)3月LVEF、LVEDD、LVESD、LAD、IVST 2组比较无明显差异(P > 0.05),达格列净组LVPWT下降明显高于常规抗心衰组(P < 0.05);(4)治疗6月及1 a,达格列净组LVEF升高程度,LAD、IVST、LVPWT下降程度明显高于常规抗心衰组(P < 0.05);治疗6月2组LVEDD、LVESD下降程度比较无统计学意义(P > 0.05),治疗1 a比较有统计学意义(P < 0.05)。  结论  在规范化抗心力衰竭药物治疗基础上,联合达格列净可以进一步改善射血分数轻度下降性心力衰竭患者的心脏重塑及心脏功能。
  • 图  1  2组LVEF治疗后比较

    Figure  1.  Comparison of LVEF between two groups after treatment

    图  2  2组LVEDD治疗后比较

    Figure  2.  Comparison of LVEDD between two groups after treatment

    表  1  2组患者的临床基线资料比较[n(%)/($ \bar x \pm s $)/M(P25P75)]

    Table  1.   Comparison of baseline clinical data in two group [n(%)/($ \bar x \pm s $)/M(P25P75)]

    基线指标 达格列净组(n = 33) 常规抗心衰组(n = 37) t/χ2/Z P
    年龄(岁) 64.09 ± 11.10 62.46 ± 13.88 0.539 0.592
    性别(男/女) 24/9 23/14 0.883 0.348
    HF病因 0.005 0.945
     缺血性心肌病 19(57.58) 21(56.76)
     非缺血性心肌病 合并疾病 14(42.42) 16(43.24)
     心房颤动 9(27.27) 11(29.73) 0.052 0.820
     高血压 22(66.67) 17(45.95) 3.035 0.081
    糖尿病用药情况 19(57.58) 16(43.24) 1.433 0.231
     ARB 10(30.30) 9(24.33) 0.315 0.574
     ACEI 6( 18.18) 8(21.62) 0.129 0.719
     ARNI 17(51.52) 20(54.05) 0.045 0.832
    β受体阻滞剂
    比索洛尔 20(60.61) 21(56.76) 0.107 0.744
    美托洛尔 13(39.39) 16(43.24) 0.107 0.744
    袢利尿剂 22(66.67) 27(72.97) 0.330 0.565
    螺内酯 33( 100.00) 37( 100.00)
    心功能分级 1.446 0.485
     II级 14(42.42) 11(29.73)
     III级 13(39.40) 16(43.24)
     IV级 6( 18.18) 10(27.03)
    收缩压(mmHg) 121.67 ± 14.33 115.57 ± 15.42 1.704 0.092
    舒张压(mmHg) 75.03 ± 10.16 74.24 ± 11.05 0.309 0.758
    心率(次/min) 75.21 ± 10.75 75.14 ± 12.53 0.027 0.978
    NT-ProBNP(pg/mL) 2 177.00(446.45 ,3 440.50) 2 086.00(826.50 ,6 711.00) −1.118 0.264
    超声心动图结果
     LVEF 0.44 ± 0.03 0.44 ± 0.03 −0.326 0.746
     LVEDD(cm) 5.62 ± 0.60 5.46 ± 0.55 1.227 0.224
     LVESD(m) 4.29 ± 0.56 4.22 ± 0.53 0.516 0.607
     LAD(cm) 4.04 ± 0.53 4.22 ± 0.85 −1.041 0.302
     IVST(cm) 1.01 ± 0.16 1.06 ± 0.22 −1.143 0.257
     LVPWT(cm) 0.98 ± 0.10 1.04 ± 0.15 −1.762 0.083
      NT-proBNP:氨基末端脑钠肽前体;HF:心力衰竭;ACEI:血管紧张素转化酶抑制剂;LVEF:左室射血分数;LVEDD:左心室 舒张末期内径;ARB:血管紧张素受体阻滞剂;LVESD:左心室收缩末期内径;LAD:左心房内径;ARNI:血管紧张素受体脑啡肽 酶抑制剂;IVST:室间隔厚度;LVPWT:左室后壁厚度。
    下载: 导出CSV

    表  2  2组患者治疗后心功能分级比较[n(%)]

    Table  2.   Comparison of cardiac functional grading after 3 months of treatment [n(%)]

    组别 n 时间 显效 有效 无效 总有效 Z P
    达格列净组 33 3 月 2(6.06) 19(57.58) 12(36.36) 21(63.64)
    6月 15(45.45) 14(42.42) 4(12.12) 29(87.88)
    1 a 22(66.67) 9(27.27) 2(6.06) 31(93.94)
    常规抗心衰组 37 3月 1(2.70) 10(27.03) 26(70.27) 11(29.73) 8.081 0.004*
    6月 11(29.73) 13(35.14) 13(35.14) 24(64.86) 5.024 0.025*
    1 a 16(43.24) 11(29.73) 10(27.03) 27(72.97) 5.398 0.020*
      ZP为2组同时期比较的检验统计量的值,*P < 0.05。
    下载: 导出CSV

    表  3  2组患者治疗后心脏超声结果比较($ \bar x \pm s $)

    Table  3.   Comparison of echocardiographic indicatorsin in two groups after treatment($ \bar x \pm s $)

    组别 时间 LVEF(%) LVEDD(cm) LVESD(cm) LAD(cm) IVST(cm) LVPWT(cm)
    达格列净组 基线 44.33 ± 3.05 5.62 ± 0.60 4.29 ± 0.56 4.04 ± 0.53 1.01 ± 0.16 0.98 ± 0.10
    3月 50.94 ± 5.37* 5.22 ± 0.66* 3.94 ± 0.67* 3.77 ± 0.55* 0.96 ± 0.18* 0.93 ± 0.13*#
    6月 54.97 ± 9.30*# 4.97 ± 0.80* 3.66 ± 0.75* 3.45 ± 0.65*# 0.90 ± 0.16*# 0.89 ± 0.12*#
    1 a 62.03 ± 9.36*# 4.58 ± 0.75*# 3.38 ± 0.70*# 3.16 ± 0.58*# 0.88 ± 0.18*# 0.87 ± 0.13*#
    常规抗心衰组 基线 44.32 ± 2.93 5.46 ± 0.55 4.22 ± 0.53 4.22 ± 0.85 1.06 ± 0.22 1.04 ± 0.15
    3月 48.41 ± 7.60* 5.28 ± 0.56* 4.00 ± 0.60* 4.02 ± 0.72* 1.01 ± 0.17* 0.99 ± 0.15*
    6月 50.43 ± 7.12* 5.15 ± 0.59* 3.85 ± 0.54* 3.90 ± 0.66* 0.99 ± 0.18* 0.90 ± 0.13*
    1 a 51.84 ± 6.81* 4.98 ± 0.68* 3.71 ± 0.55* 3.75 ± 0.66* 0.97 ± 0.16* 0.96 ± 0.02*
      同组治疗前后比较,*P < 0.05;与常规抗心衰组治疗后比较,# P < 0.05。
    下载: 导出CSV

    表  4  2组不良反应发生率比较[n(%)]

    Table  4.   Comparison of occurrence of adverse effect [n(%)]

    组别 n 低血糖 低血压 尿路感染 肾功能损伤
    达格列净组 33 0(0.00) 0(0.00) 1(3.03) 0(0.00)
    常规抗心衰组 37 3(8.11) 3(8.11) 0(0.00) 5(13.51)
    χ2 1.168 1.168 2.981
    P 0.280 0.280 0.471 0.084
    下载: 导出CSV
  • [1] Zhang Y,Zhang J,Butler J,et al. China-HF innvestigators. Contemporary epidemiology,eanagement,and outcomes of patients hospitalized for heart failure in China: Results from the China heart failure ( China-HF) registry[J]. J Card Fail,2017,23(12):868-875. doi: 10.1016/j.cardfail.2017.09.014
    [2] McDonagh T A,Metra M,Adamo M,et al. ESC scientific document group. 2021 ESC guidelines for the diagnosis and treatment of acute and chronic heart failure[J]. Eur Heart J,2021,42(36):3599-3726. doi: 10.1093/eurheartj/ehab368
    [3] Heidenreich P A,Bozkurt B,Aguilar D,et al. 2022 AHA/ACC/HFSA guideline for the management of heart failure: Executive summary: A report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines[J]. J Am Coll Cardiol,2022,79(17):1757-1780. doi: 10.1016/j.jacc.2021.12.011
    [4] McMurray J J V,Solomon S D,Inzucchi S E,et al. DAPA-HF trial committees and investigators. Dapagliflozin in patients with heart failure and reduced ejection fraction[J]. N Engl J Med,2019,381(21):1995-2008. doi: 10.1056/NEJMoa1911303
    [5] Savarese G,Stolfo D,Sinagra G,et al. Heart failure with mid-range or mildly reduced ejection fraction[J]. Nat Rev Cardiol,2022,19(2):100-116. doi: 10.1038/s41569-021-00605-5
    [6] Chioncel O,Lainscak M,Seferovic P M,et al. Epidemiology and one-year outcomes in patients with chronic heart failure and preserved,mid-range and reduced ejection fraction: An analysis of the ESC heart failure long-term registry[J]. Eur J Heart Fail,2017,19(12):1574-1585. doi: 10.1002/ejhf.813
    [7] 中华医学会心血管病学分会心力衰竭学组,中国医师协会心力衰竭专业委员会,中华心血管病杂志编辑委员会. 中国心力衰竭诊断和治疗指南2018[J]. 中华心血管病杂志,2018,46(10):760-789.
    [8] Solomon S D,De Boer R A,DeMets D,et al. Dapagliflozin in heart failure with preserved and mildly reduced ejection fraction: Rationale and design of the DELIVER trial[J]. Eur J Heart Fail,2021,23(7):1217-1225. doi: 10.1002/ejhf.2249
    [9] Cure E,Cumhur Cure M. Comment on: "High released lactate by epicardial fat from coronary artery disease patients is reduced by dapagliflozin treatment"[J]. Atherosclerosis,2020,296(1):2-3.
    [10] Das U S,Paul A,Banerjee S. SGLT2 inhibitors in heart failure with reduced ejection fraction[J]. Egypt Heart J,2021,73(1):93-99. doi: 10.1186/s43044-021-00218-w
    [11] Butt J H,Lu H,Kondo T,et al. Heart failure,chronic obstructive pulmonary disease and efficacy and safety of dapagliflozin in heart failure with mildly reduced or preserved ejection fraction: Insights from DELIVER[J]. Eur J Heart Fail,2023,25(11):2078-2090. doi: 10.1002/ejhf.3000
    [12] Solomon S D,Vaduganathan M,L Claggett B,et al. Sacubitril/valsartan across the spectrum of ejection fraction in heart failure[J]. Circulation,2020,141(5):352-361. doi: 10.1161/CIRCULATIONAHA.119.044586
    [13] Anker S D,Butler J,Filippatos G,et al. EMPEROR-preserved trial investigators. Empagliflozin in heart failure with a preserved ejection fraction[J]. N Engl J Med,2021,385(16):1451-1461. doi: 10.1056/NEJMoa2107038
    [14] Solomon S D,McMurray J,Claggett B,et al. DELIVER trial committees and investigators. Dapagliflozin in heart failure with mildly reduced or preserved ejection fraction[J]. N Engl J Med,2022,387(12):1089-1098. doi: 10.1056/NEJMoa2206286
    [15] Lee M M Y,Brooksbank K J M,Wetherall K,et al. Effect of empagliflozin on left ventricular volumes in patients with type 2 diabetes,or prediabetes,and heart failure with reduced ejection fraction (SUGAR-DM-HF)[J]. Circulation,2021,143(6):516-525. doi: 10.1161/CIRCULATIONAHA.120.052186
    [16] Santos-Gallego C G,Vargas-Delgado A P,Requena-Ibanez J A,et al. EMPA-TROPISM (ATRU-4) investigators. Randomized trial of empagliflozin in nondiabetic patients with heart failure and reduced ejection fraction[J]. J Am Coll Cardiol,2021,77(3):243-255. doi: 10.1016/j.jacc.2020.11.008
    [17] Chan Y H,Hsu T J,Wang C L,et al. Sodium glucose cotransporter-2 inhibitor was associated with an improvement in left ventricular systolic function in patients with type 2 diabetes mellitus with impaired left ventricular systolic function[J]. ESC Heart Fail,2020,7(5):2784-2796. doi: 10.1002/ehf2.12877
    [18] Lan N S R,Fegan P G,Yeap B B,et al. The effects of sodium-glucose cotransporter 2 inhibitors on left ventricular function: Current evidence and future directions[J]. ESC Heart Fail,2019,6(5):927-935. doi: 10.1002/ehf2.12505
    [19] Mudaliar S,Alloju S,Henry R R. Can a shift in fuel energetics explain the beneficial cardiorenal outcomes in the EMPA-REG OUTCOME study? A unifying hypothesis[J]. Diabetes Care,2016,39(7):1115-1122. doi: 10.2337/dc16-0542
    [20] Yurista S R,Silljé H H W,Van Goor H,et al. Effects of sodium-glucose co-transporter 2 inhibition with empaglifozin on renal structure and function in non-diabetic rats with left ventricular dysfunction after myocardial infarction[J]. Cardiovasc Drugs Ther,2020,34(3):311-321. doi: 10.1007/s10557-020-06954-6
    [21] Lee T M,Chang N C,Lin S Z. Dapagliflozin,a selective SGLT2 inhibitor,attenuated cardiac fibrosis by regulating the macrophage polarization via STAT3 signaling in infarcted rat hearts[J]. Free Radic Biol Med,2017,104(1):298-310.
    [22] Lupón J,Gavidia-Bovadilla G,Ferrer E,et al. Heart failure with preserved ejection fraction infrequently evolves toward a reduced phenotype in long-term survivors[J]. Circ Heart Fail,2019,12(3):e005652. doi: 10.1161/CIRCHEARTFAILURE.118.005652
    [23] Miller R J H,Nabipoor M,Youngson E,et al. Heart failure with mildly reduced ejection fraction: Retrospective study of ejection fraction trajectory risk[J]. ESC Heart Fail,2022,9(3):1564-1573. doi: 10.1002/ehf2.13869
    [24] Uthman L,Homayr A,Juni R P,et al. Empagliflozin and dapagliflozin reduce ROS generation and restore NO bioavailability in tumor necrosis factor α-stimulated human coronary arterial endothelial cells[J]. Cell Physiol Biochem,2019,53(5):865-886. doi: 10.33594/000000178
    [25] Wiviott S D,Raz I,Bonaca M P,et al. Dapagliflozin and cardiovascular outcomes in type 2 diabetes[J]. N Engl J Med,2019,380(4):347-357. doi: 10.1056/NEJMoa1812389
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出版历程
  • 收稿日期:  2024-05-12
  • 网络出版日期:  2024-11-09
  • 刊出日期:  2024-11-25

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