达格列净对不伴糖尿病的心力衰竭患者血尿酸的影响

林梦娇. 达格列净对不伴糖尿病的心力衰竭患者血尿酸的影响[J]. 临床心血管病杂志, 2025, 41(1): 24-27. doi: 10.13201/j.issn.1001-1439.2025.01.007
引用本文: 林梦娇. 达格列净对不伴糖尿病的心力衰竭患者血尿酸的影响[J]. 临床心血管病杂志, 2025, 41(1): 24-27. doi: 10.13201/j.issn.1001-1439.2025.01.007
LIN Mengjiao. Effects of dapagliflozin on serum uric acid in non-diabetic patients with heart failure[J]. J Clin Cardiol, 2025, 41(1): 24-27. doi: 10.13201/j.issn.1001-1439.2025.01.007
Citation: LIN Mengjiao. Effects of dapagliflozin on serum uric acid in non-diabetic patients with heart failure[J]. J Clin Cardiol, 2025, 41(1): 24-27. doi: 10.13201/j.issn.1001-1439.2025.01.007

达格列净对不伴糖尿病的心力衰竭患者血尿酸的影响

  • 基金项目:
    通用医疗科研基金(No:TYYLKYJJ-2022-025)
详细信息

Effects of dapagliflozin on serum uric acid in non-diabetic patients with heart failure

More Information
  • 目的  探讨达格列净对不伴糖尿病的心力衰竭患者血尿酸的影响。 方法  选取2023年1月—2024年1月于哈尔滨二四二医院住院的心力衰竭合并高尿酸血症并不伴糖尿病患者200例,随机分为试验组(达格列净+心力衰竭标准治疗)和对照组(心力衰竭标准治疗),每组100例。记录两组患者治疗前后尿酸、氨基末端脑钠肽前体(NT-proBNP)和左室射血分数(LVEF)。随访6个月,观察痛风发作和不良事件发生情况。 结果  治疗7 d和6个月后,对照组尿酸水平较治疗前均显著上升(均P<0.05),试验组尿酸水平较治疗前均显著下降(均P<0.05)。治疗6个月后,对照组LVEF改善不明显,NT-proBNP水平显著下降(P<0.05);试验组LVEF显著升高,NT-proBNP水平显著下降(均P<0.05)。随访期间,试验组痛风发生率显著低于对照组(4.2% vs 22.3%,P<0.05)。对照组和试验组均未发生低血糖、低血压、酮症酸中毒、急性肾损伤或肾功能损害等事件;与对照组相比较,试验组泌尿生殖系感染发生率升高(9.4% vs 2.1%,P=0.032)、心血管死亡率降低(0.06% vs 0,P=0.013)、住院率降低(25.5% vs 0.08%,P=0.002)。 结论  达格列净整体安全性良好,能有效降低不伴糖尿病的心衰患者的血尿酸水平,减少痛风发作,降低心衰恶化风险,改善长期预后。
  • 加载中
  • 表 1  基本资料

    Table 1.  General data 例(%), X±S

    项目 对照组(94例) 试验组(96例) P
    女/男 48/46 48/48 0.883
    年龄/岁 73.9±9.4 72.4±9.7 0.305
    BMI/(kg/m2) 25.5±3.7 25.2±2.7 0.474
    收缩压/mmHg 130.7±12.6 133.2±12.1 0.163
    舒张压/mmHg 71.4±6.6 70.4±7.8 0.318
    空腹血糖/(mmol/L) 5.4±0.5 5.2±0.5 0.070
    糖化血红蛋白/% 5.0±0.5 5.2±0.5 0.068
    eGFR/(mL/min/1.73m2) 80.4±6.0 79.2±5.5 0.167
    尿酸/(μmol/L) 478.4±52.7 489.8±44.2 0.108
    NYHA分级 0.571
      Ⅲ 51(54.3) 56(58.3)
      Ⅳ 43(45.7) 40(41.7)
    LVEF/% 43.5±8.2 42.4±8.9 0.357
    心衰分型 0.901
      HFrEF 37(39.4) 35(36.5)
      HFmrEF 27(28.7) 30(31.3)
      HFpEF 30(31.9) 31(32.2)
    NT-proBNP/(ng/L) 1 693.1±280.7 1 665.3±286.5 0.500
    基础疾病
      高血压 27(28.7) 26(27.1) 0.801
      缺血性心肌病 48(51.1) 51(53.1) 0.776
      扩张型心肌病 9(9.6) 7(7.3) 0.571
      心房颤动 10(10.6) 12(12.5) 0.688
    合并用药
      沙库巴曲缬沙坦 83(88.3) 85(88.5) 0.958
      β受体阻滞剂 82(87.2) 78(81.3) 0.258
      螺内酯 90(95.7) 92(95.8) 0.976
      利尿剂 94(100) 96(100) 1.000
      地高辛 85(90.4) 87(90.6) 0.963
      阿司匹林 57(60.6) 63(65.6) 0.476
      他汀类 70(74.5) 61(63.5) 0.104
    下载: 导出CSV

    表 2  治疗前后尿酸水平比较

    Table 2.  Uric acid levels before and after treatment μmol/L, X±S

    组别 治疗前 治疗后
    7 d 6个月
    对照组(94例) 478.4±52.7 494.4±50.22) 546.3±59.22)
    试验组(96例) 489.8±44.2 461.4±41.41)2) 395.3±45.41)2)
    与对照组同期比较,1)P<0.05;与同组治疗前比较,2)P<0.05。
    下载: 导出CSV

    表 3  治疗前后LVEF和NT-proBNP水平比较

    Table 3.  LVEF and NT-proBNP levels before and after treatment X±S

    项目 对照组(94例) 试验组(96例)
    LVEF/%
      治疗前 43.5±8.2 42.4±8.9
      治疗6个月 45.7±6.7 49.3±5.71)2)
    NT-proBNP/(ng/L)
      治疗前 1 693.1±280.7 1 665.3±286.5
      治疗6个月 1 457.1±304.11) 1 273.3±287.81)2)
    与同组治疗前比较,1)P<0.05;与对照组同期比较,2)P<0.05。
    下载: 导出CSV
  • [1]

    McMurray JJV, Packer M. How should we sequence the treatments for heart failure and a reduced ejection fraction? A redefinition of evidence-based medicine[J]. Circulation, 2021, 143(9): 875-877. doi: 10.1161/CIRCULATIONAHA.120.052926

    [2]

    Mcdonagh TA, Metra M, Adamo M, et al. 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]

    Winder M, Owczarek AJ, Mossakowska M, et al. Prevalence of Hyperuricemia and the Use of Allopurinol in Older Poles-Results from a Population-Based PolSenior Study[J]. Int J Environ Res Public Hralth, 2021, 18(2): 387. doi: 10.3390/ijerph18020387

    [4]

    Muiesan ML, Salvetti M, Virdis A, et al. Serum uric acid, pre-dicts heart failure in a large Italian cohort: search for a cut-off value the uric acid right for heart health study[J]. J Hypertens, 2021, 39(1): 62-69. doi: 10.1097/HJH.0000000000002589

    [5]

    Doehner W, Anker SD, Butler J, et al. Uric acid and sodium-lucose cotransporter-2 inhibition with empagliflozin in heart fai-ure with reduced ej ection fraction: the EMPEROR-reduced trial[J]. Eur Heart J, 2022, 43(36): 3435-3446. doi: 10.1093/eurheartj/ehac320

    [6]

    Zannad F, Ferreira JP, Pocock SJ, et al. SGLT2 inhibitors in patients with heart failure with reduced ejection fraction: a meta-analysis of the EMPEROR-Reduced and DAPA-HF trials[J]. Lancet, 2020, 396(10254): 819-829. doi: 10.1016/S0140-6736(20)31824-9

    [7]

    Kittleson MM, Panjrath GS, Amancherla K, et al. 2023 ACC Expert Consensus Decision Pathway on Management of Heart Failure With Preserved Ejection Fraction: A Report of the American College of Cardiology Solution Set Oversight Committee[J]. J Am Coll Cardiol, 2023, 81(18): 1835-1878. doi: 10.1016/j.jacc.2023.03.393

    [8]

    Zhao D, Liu H, Dong P. Empagliflozin reduces blood pressure and uric acid in patients with type 2 diabetes mellitus: a systematic review and meta-analysis[J]. J Hum Hypertens, 2019, 33(4): 327-339. doi: 10.1038/s41371-018-0134-2

    [9]

    Heidenreich PA, Bozkurt B, Aguilar D, et al. 2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines[J]. Circulation, 2022, 145(18): e895-e1032.

    [10]

    Sung SH, Chuang SY, Liu WL, etal. Hyperuricemiaandpulse pressure are predictive ofincident heart failure in an elderly population[J]. IntJ Cardiol, 2020, 300: 178-183. doi: 10.1016/j.ijcard.2019.11.001

    [11]

    Aguilar-Gallardo JS, Correa A, Contreras JP. Cardio-renal benefits of sodium-glucose co-transporter 2 inhibitors in heart failure with reduced ejection fraction: mechanisms and clinical evidence[J]. Eur Heart J Cardiovasc Pharmacother, 2022, 8(3): 311-321. doi: 10.1093/ehjcvp/pvab056

    [12]

    Joshi SS, Singh T, Newby DE, et al. Sodium-glucose cotransporter 2 inhibitor therapy: mechanisms of action in heart failure[J]. Heart, 2021, 107(13): 1032-1038. doi: 10.1136/heartjnl-2020-318060

    [13]

    Nassif ME, Windsor SL, Borlaug BA, et al. The SGLT2 inhibitor dapagliflozin in heart failure with preserved ejection fraction: a multicenter randomized trial[J]. Nat Med, 2021, 27(11): 1954-1960. doi: 10.1038/s41591-021-01536-x

    [14]

    Solomon SD, de Boer RA, 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

    [15]

    Bhatt DL, Verma S, Pitt B. EMPEROR-Preserved: Apromise fulfilled[J]. Cell Metabol, 2021, 33(11): 2099-2103. doi: 10.1016/j.cmet.2021.10.011

    [16]

    Spertus JA, Birmingham MC, Nassif M, et al. The SGLT2 inhibitor canagliflozin in heart failure: the CHIEF-HF remote, patient-centered randomized trial[J]. Nat Med, 2022, 28(4): 809-813. doi: 10.1038/s41591-022-01703-8

    [17]

    Ahmadieh H, Azar S. Effects of Sodium Glucose Cotransporter-2 Inhibitors on Serum Uric Acid in Type 2 Diabetes Mellitus[J]. Diabetes Technol Ther, 2017, 19(9): 507-512. doi: 10.1089/dia.2017.0070

    [18]

    蒋达成. 达格列净在Nrf2/Keap1信号通路中降尿酸效果的研究[D]. 南昌: 南昌大学, 2020.

    [19]

    Novikov A, Fu Y, Huang W, et al. SGLT2 inhibition and renal urate excretion: role of luminal glucose, GLUT9, and URAT1[J]. Am J Physiol Renal Physiol, 2019, 316(1): F173-f185. doi: 10.1152/ajprenal.00462.2018

    [20]

    Lappas M, Andrikopoulos S, Permezel M. Hypoxanthine-xanthine oxidase down-regulates GLUT1 transcription via SIRT1 resulting in decreased glucose uptake in human placenta[J]. J Endocrinol, 2012, 213(1): 49-57. doi: 10.1530/JOE-11-0355

    [21]

    Kaneko M, Narukawa M. Effects of sodium-glucose cotransport-er 2 inhibitors on amputation, bone fracture, and cardiovascular outcomes in patients with type 2 diabetes mellitus using an alter-native measure to the hazard ratio[J]. Clin Drug Investig, 2019, 39: 179-186. doi: 10.1007/s40261-018-0731-4

    [22]

    Wiviott SD, Raz I, Bonaca MP, et al. Dapagliflozin and cardio-vascularoutcomesin type2diabetes[J]. Nengl J Med, 2019, 380(4): 347-357. doi: 10.1056/NEJMoa1812389

  • 加载中
计量
  • 文章访问数:  831
  • PDF下载数:  31
  • 施引文献:  0
出版历程
收稿日期:  2024-06-06
刊出日期:  2025-01-13

目录