达格列净对2型糖尿病伴慢性心力衰竭患者的疗效及心外膜脂肪厚度影响
Efficacy of Dapagliflozin on Type 2 Diabetic Patients with Chronic Heart Failure and Its Effect on Thickness of Epicardial Adipose Tissue
DOI: 10.12677/ACRVM.2022.101001, PDF,   
作者: 叶炳华*#, 史爱梅:江苏省泰州市第三人民医院心内科,江苏 泰州;杨淑芳:江苏省泰州市人民医院内分泌科,江苏 泰州;唐宝康, 戚文群:江苏省泰州市第三人民医院内分泌科,江苏 泰州;李伯堂:江苏省泰州市第三人民医院超声科,江苏 泰州
关键词: 达格列净慢性心力衰竭N-端脑钠肽前体6分钟步行试验心外膜脂肪Dapagliflozin Chronic Heart Failure N-Terminal Pro-Brain Natriuretic Peptide 6-Minute Walking Test Epicardial Adipose Tissue
摘要: 目的:观察达格列净对2型糖尿病(T2DM)伴慢性心力衰竭(CHF)患者的临床疗效以及对心外膜脂肪(EAT)厚度的影响。方法:选择2018年8月~2021年01月住院的T2DM伴心功能II~IV级CHF患者72例,随机分为治疗组和对照组各36例,两组基础治疗相同,治疗组加用达格列净,6个月后分别比较两组患者治疗前后及两组之间EAT厚度、左房前后径(LAD)、左室舒张末内径(LVDd)、左室射血分数(LVEF)、糖化血红蛋白(HbA1c)、N端脑钠肽前体(NT-proBNP)水平、6分钟步行试验(6MWT)及生活质量变化,并观察治疗效果、再住院人次及药物不良反应。结果:与治疗前相比,治疗组EAT厚度明显降低(P < 0.01),对照组无明显变化,两组治疗后LAD、LVDd、HbA1c、NT-proBNP、生活质量评分均明显下降,6MWT、LVEF明显提高(P < 0.01);治疗后组间比较,两组除LAD外,其他指标均有显著差异,以治疗组为优(P < 0.05或0.01);治疗组显效率优于对照组(P < 0.01),但总有效率与对照组无统计学差异(P > 0.05);治疗组再入院人次较对照组减低(P < 0.05),两组不良反应发生率相似(P > 0.05)。结论:T2DM伴CHF患者加用达格列净能进一步改善患者心功能,提高生活质量,降低再住院次数,使用安全性高,降低EAT厚度可能是其中一个机制。
Abstract: Objective: To observe the clinical effect of Dapagliflozin on type 2 diabetes mellitus (T2DM) patients with chronic heart failure (CHF) and the influence on the thickness of epicardial adipose tissue (EAT). Methods: 72 T2DM patients with CHF of cardiac function grade II~IV who were hospitalized from August 2018 to January 2021 were randomly divided into treatment group (N = 36) and control group (N = 36). The basic treatment was the same in both groups, and Dagligliflozin was added to the treatment group. After 6 months, thickness of EAT, left atrial anter-oposterior diameter (LAD), left ventricular end-diastolic diameter (LVDd), left ventricular ejection fraction (LVEF), hemoglobin A1c (HbA1c), N-terminal pro-brain natriuretic peptide (NT-proBNP), 6-minute walking test (6MWT) and quality of life were compared before and after treatment and between the two groups. At the same time, the therapeutic effect, the number of readmission and drug reactions were observed. Results: Compared with pre-treatment, the thickness of EAT in the treatment group was significantly decreased (P < 0.01), and there was no significant change in the control group. After treatment, the scores of LAD, LVDd, HbA1c, NT-proBNP and quality of life in the two groups were significantly decreased, and 6 MWT and LVEF were significantly increased (P < 0.01). Except LAD, there were significant differences in other indexes between the two groups, the treatment group was better than the control group (P < 0.05 or 0.01). The effective rate of the treatment group was better than that of the control group (P < 0.01), but there was no significant difference in the total effective rate between the two groups (P > 0.05). The number of readmission in the treatment group was significantly lower than that in the control group (P < 0.05), and the incidence of adverse reactions was similar in the two groups (P > 0.05). Conclusion: Adding Dapagliflozin to T2DM patients with CHF can improve heart function, improve the quality of life, reduce the number of readmission, and can use safely. One of the mechanisms may be related to reducing the thickness of EAT.
文章引用:叶炳华, 杨淑芳, 唐宝康, 戚文群, 史爱梅, 李伯堂. 达格列净对2型糖尿病伴慢性心力衰竭患者的疗效及心外膜脂肪厚度影响[J]. 亚洲心脑血管病例研究, 2022, 10(1): 1-7. https://doi.org/10.12677/ACRVM.2022.101001

参考文献

[1] Zinman, B., Wanner, C., Lachin, J.M., et al. (2015) Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. The New England Journal of Medicine, 373, 2117-2128. [Google Scholar] [CrossRef
[2] Bhatt, D.L., Verma, S. and Braunwald, E. (2019) The DAPA-HF Trial: A Momentous Victory in the War against Heart Failure. Cell Metabolism, 30, 847-849. [Google Scholar] [CrossRef] [PubMed]
[3] Neal, B., Perkovic, V., Mahaffey, K.W., et al. (2017) Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes. The New England Journal of Medicine, 377, 644-657. [Google Scholar] [CrossRef
[4] Wiviott, S.D., Raz, I., Bonaca, M.P., et al. (2019) Dapagliflozin and Cardiovascular Outcomes in Type 2 Diabetes. The New England Journal of Medicine, 380, 347-357. [Google Scholar] [CrossRef
[5] 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.
[6] 中华医学会糖尿病学分会. 中国2型糖尿病防治指南(2017年版) [J]. 中华糖尿病杂志, 2018, 10(1): 4-67.
[7] 中华医学会超声医学分会超声心电图学组. 中国成年人超声心动图检查测量指南[J]. 中华超声影像学杂志, 2016, 25(8): 645-666.
[8] Heerspink, H.J., Perkins, B.A., Fitchett, D.H., et al. (2016) Sodium Glucose Cotransporter 2 Inhibitors in the Treatment of Diabetes Mellitus: Cardiovascular and Kidney Effects, Potential Mechanisms, and Clinical Applications. Circulation, 134, 752-772. [Google Scholar] [CrossRef
[9] Uthman, L., Baartscheer, A., Bleijlevens, B., et al. (2018) Class Effects of SGLT2 Inhibitors in Mouse Cardiomyocytes and Hearts: Inhibition of Na+/H+ Exchanger, Lowering of Cytosolic Na+ and Vasodilation. Diabetologia, 61, 722-726. [Google Scholar] [CrossRef] [PubMed]
[10] McMurray, J.J.V., DeMets, D.L., Inzucchi, S.E., et al. (2019) A Trial to Evaluate the Effect of the Sodium Glucose Cotransporter 2 Inhibitor Dapagliflozin on Morbidity and Mortality in Patients with Heart Failure and Reduced Left Ventricular Ejection Fraction (DAPA-HF). European Journal of Heart Failure, 21, 665-675. [Google Scholar] [CrossRef] [PubMed]
[11] Lan, N.S.R., Fegan, P.G., Yeap, B.B., et al. (2019) The Effects of Sodium-Glucose Cotransporter 2 Inhibitors on Left Ventricular Function: Current Evidence and Future Directions. ESC Heart Failure, 6, 927-935. [Google Scholar] [CrossRef] [PubMed]
[12] Packer, M., Greene, S.J., Fiuzat, M., et al. (2019) Heart Failure Endpoints in Cardiovascular Outcome Trials of SGLT2 Inhibitors in Patients with Type 2 Diabetes: A Critical Evaluation of Clinical and Regulatory Issues. Circulation, 140, 2108-2118. [Google Scholar] [CrossRef
[13] Mazurek, T., Zhang, L., Zalewski, A., et al. (2003) Human Epicardial Adipose Tissue Is a Source of Inflammatory Mediators. Circulation, 108, 2460-2466. [Google Scholar] [CrossRef
[14] Blumensatt, M., Fahlbusch, P., Hilgers, R., et al. (2017) Secretory Products from Epicardial Adipose Tissue from Patients with Type 2 Diabetes Impair Mitochondrial β-Oxidation in Cardiomyocytes via Activation of the Cardiac Renin-Angiotensin System and Induction of miR-208a. Basic Research in Cardiology, 112, 2. [Google Scholar] [CrossRef] [PubMed]
[15] Chechi, K., Voisine, P., Mathieu, P., et al. (2017) Functional Characterization of the Ucp1-Associated Oxidative Phenotype of Human Epicardial Adipose Tissue. Scientific Reports, 7, Article No. 5566. [Google Scholar] [CrossRef] [PubMed]
[16] Sugita, Y., Ito, K., Sakurai, S., et al. (2020) Epicardial Adipose Tissue Is Tightly Associated with Exercise Intolerance in Patients with Type 2 Diabetes Mellitus with Asymptomatic Left Ventricular Structural and Functional Abnormalities. Journal of Diabetic Complications, 34, Article ID: 107552. [Google Scholar] [CrossRef] [PubMed]
[17] Christensen, R.H., Hansen, C.S., von Scholten, B.J., et al. (2019) Epicardial and Pericardial Adipose Tissues Are Associated with Reduced Diastolic and Systolic Function in Type 2 Diabetes. Diabetes, Obesity and Metabolism, 21, 2006-2011. [Google Scholar] [CrossRef] [PubMed]
[18] Shah, R.V. anderson, A., Ding, J., et al. (2017) Pericardial, But Not Hepatic, Fat by Computed Tomography Is Associated with Cardiovascular Outcomes and Structure: The Multi-Ethnic Study of Atherosclerosis (MESA). JACC: Cardiovascular Imaging, 10, 1016-1027. [Google Scholar] [CrossRef] [PubMed]
[19] Levelt, E., Pavlides, M., Banerjee, R., et al. (2016) Ectopic and Visceral Fat Deposition in Lean and Obese Patients with Type 2 Diabetes. Journal of the American College of Cardiology, 68, 53-63. [Google Scholar] [CrossRef] [PubMed]
[20] Drapkina, O.M. and Zyatenkova, E.V. (2016) Evaluation of Cardiovascular Remodeling and Epicardial Fat Thickness in Patients with Chronic Heart Failure and Metabolic Syndrome. Terapevticheskii Arkhiv, 88, 64-70. [Google Scholar] [CrossRef] [PubMed]
[21] 蒋凌云, 颜晓东, 韦洁明. 初诊2型糖尿病患者内脏脂肪含量与心功能的相关性研究[J]. 中华糖尿病杂志, 2020, 12(4): 236-240.
[22] 刘福成, 单光华, 边宁, 等. 稳定性冠心病患者心外膜脂肪组织与N端脑利钠肽前体水平的相关性研究[J]. 中国病理生理杂志, 2015, 17(9): 1617-1620.
[23] Sato, T., Aizawa, Y., Yuasa, S., et al. (2018) The Effect of Dapagliflozin Treatment on Epicardial Adipose Tissue Volume. Cardiovascular Diabetology, 17, 6. [Google Scholar] [CrossRef] [PubMed]
[24] Yagi, S., Hirata, Y., Ise, T., et al. (2017) Canagliflozin Reduces Epicardial Fat in Patients with Type 2 Diabetes Mellitus. Diabetology & Metabolic Syndrome, 9, 78. [Google Scholar] [CrossRef] [PubMed]