Clinical Focus ›› 2021, Vol. 36 ›› Issue (8): 713-718.doi: 10.3969/j.issn.1004-583X.2021.08.008
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Yin Xiaokang1, Zhang Jiping2, Zhu Yugang3, Shen Hongxia3, Wang Defeng3()
Received:
2021-04-06
Online:
2021-08-20
Published:
2021-08-30
Contact:
Wang Defeng
E-mail:wdf991217@126.com
CLC Number:
Yin Xiaokang, Zhang Jiping, Zhu Yugang, Shen Hongxia, Wang Defeng. Effect of empagliflozin on ventricular remodeling in patients with type 2 diabetes mellitus and coronary heart disease[J]. Clinical Focus, 2021, 36(8): 713-718.
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URL: https://huicui.hebmu.edu.cn/EN/10.3969/j.issn.1004-583X.2021.08.008
组别 | 例数 | 性别(例) | 年龄 (岁) | 体质量指数 (kg/m2) | 病程 (年) | |
---|---|---|---|---|---|---|
男 | 女 | |||||
试验组 | 64 | 36 | 28 | 48±12.48 | 24.97±3.57 | 8.56±7.03 |
对照组 | 64 | 34 | 30 | 50±11.75 | 25.16±3.92 | 8.92±7.64 |
统计值 | χ2=0.032 | t=0.285 | t=0.179 | t=0.862 | ||
P值 | 0.859 | 0.776 | 0.858 | 0.390 |
组别 | 例数 | 性别(例) | 年龄 (岁) | 体质量指数 (kg/m2) | 病程 (年) | |
---|---|---|---|---|---|---|
男 | 女 | |||||
试验组 | 64 | 36 | 28 | 48±12.48 | 24.97±3.57 | 8.56±7.03 |
对照组 | 64 | 34 | 30 | 50±11.75 | 25.16±3.92 | 8.92±7.64 |
统计值 | χ2=0.032 | t=0.285 | t=0.179 | t=0.862 | ||
P值 | 0.859 | 0.776 | 0.858 | 0.390 |
组别 | 例数 | BNP(pg/ml) | 肌钙蛋白I(μg/L) | CK-MB(U/L) | |||
---|---|---|---|---|---|---|---|
治疗前 | 治疗后 | 治疗前 | 治疗后 | 治疗前 | 治疗后 | ||
对照组 | 64 | 105.41±10.13 | 101.32±11.32 | 0.14±0.12 | 0.12±0.06 | 14.65±5.46 | 14.16±4.63 |
试验组 | 64 | 108.74±12.94 | 102.25±10.62 | 0.13±0.15 | 0.11±0.04 | 14.37±5.35 | 13.82±4.12 |
t值 | 0.599 | 1.246 | 0.698 | 1.641 | 0.156 | 1.848 | |
P值 | 0.550 | 0.215 | 0.486 | 0.103 | 0.876 | 0.067 |
组别 | 例数 | BNP(pg/ml) | 肌钙蛋白I(μg/L) | CK-MB(U/L) | |||
---|---|---|---|---|---|---|---|
治疗前 | 治疗后 | 治疗前 | 治疗后 | 治疗前 | 治疗后 | ||
对照组 | 64 | 105.41±10.13 | 101.32±11.32 | 0.14±0.12 | 0.12±0.06 | 14.65±5.46 | 14.16±4.63 |
试验组 | 64 | 108.74±12.94 | 102.25±10.62 | 0.13±0.15 | 0.11±0.04 | 14.37±5.35 | 13.82±4.12 |
t值 | 0.599 | 1.246 | 0.698 | 1.641 | 0.156 | 1.848 | |
P值 | 0.550 | 0.215 | 0.486 | 0.103 | 0.876 | 0.067 |
组别 | 例数 | LVEDV(ml) | LVESV(ml) | LVEF(%) | LVFS(%) | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | 64 | 123.54±12.69 | 114.68±13.78* | 64.75±5.65 | 55.82±6.37* | 62.73±5.64 | 63.25±4.32 | 25.35±1. 51 | 27.18±1.83* | |||||||
试验组 | 64 | 121.37±15.13 | 108.94±12.95*# | 62.86±6.49 | 52.19±5.64*# | 63.35±5.48 | 64.76±3.86 | 25.84±1.65 | 28.79±1.28*# | |||||||
t值 | 1.025 | 4.169 | 0.661 | 5.327 | 0.854 | 1.635 | 1.265 | 4.386 | ||||||||
P值 | 0.307 | 0.000 | 0.510 | 0.000 | 0.395 | 0.105 | 0.208 | 0.000 | ||||||||
组别 | 例数 | LVEDD(mm) | LVESD(mm) | IVS(mm) | LVPW(mm) | |||||||||||
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 | 64 | 62.64±3.42 | 57.93±2.12* | 51.29±4.35 | 48.13±3.58* | 14.82±0.58 | 12.32±0.43* | 14.39±0.46 | 14.03±0.84* | |||||||
试验组 | 64 | 63.53±5.37 | 56.71±4.94*# | 52.37±4.71 | 46.83±3.12*# | 13.68±0.41 | 10.97±0.75*# | 13.97±0.76 | 12.56±0.68*# | |||||||
t值 | 0.258 | 6.137 | 0.324 | 5.789 | 0.166 | 7.374 | 0.812 | 7.842 | ||||||||
P值 | 0.798 | 0.000 | 0.746 | 0.000 | 8.868 | 0.000 | 0.418 | 0.000 |
组别 | 例数 | LVEDV(ml) | LVESV(ml) | LVEF(%) | LVFS(%) | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | 64 | 123.54±12.69 | 114.68±13.78* | 64.75±5.65 | 55.82±6.37* | 62.73±5.64 | 63.25±4.32 | 25.35±1. 51 | 27.18±1.83* | |||||||
试验组 | 64 | 121.37±15.13 | 108.94±12.95*# | 62.86±6.49 | 52.19±5.64*# | 63.35±5.48 | 64.76±3.86 | 25.84±1.65 | 28.79±1.28*# | |||||||
t值 | 1.025 | 4.169 | 0.661 | 5.327 | 0.854 | 1.635 | 1.265 | 4.386 | ||||||||
P值 | 0.307 | 0.000 | 0.510 | 0.000 | 0.395 | 0.105 | 0.208 | 0.000 | ||||||||
组别 | 例数 | LVEDD(mm) | LVESD(mm) | IVS(mm) | LVPW(mm) | |||||||||||
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 | 64 | 62.64±3.42 | 57.93±2.12* | 51.29±4.35 | 48.13±3.58* | 14.82±0.58 | 12.32±0.43* | 14.39±0.46 | 14.03±0.84* | |||||||
试验组 | 64 | 63.53±5.37 | 56.71±4.94*# | 52.37±4.71 | 46.83±3.12*# | 13.68±0.41 | 10.97±0.75*# | 13.97±0.76 | 12.56±0.68*# | |||||||
t值 | 0.258 | 6.137 | 0.324 | 5.789 | 0.166 | 7.374 | 0.812 | 7.842 | ||||||||
P值 | 0.798 | 0.000 | 0.746 | 0.000 | 8.868 | 0.000 | 0.418 | 0.000 |
[1] | 杨文英. 中国糖尿病的流行特点及变化趋势[J]. 中国科学:生命科学, 2018, 48(8):812-819. |
[2] |
Samukawa Y, Haneda M, Seino Y, et al. Pharmacokinetics and pharmacodynamics of luseogliflozin, a selective SGLT2 inhibitor, in Japanese patients with type 2 diabetes with mild to severe renal impairment[J]. Clin Pharmacol Drug Dev, 2018, 7(8):820-828.
doi: 10.1002/cpdd.v7.8 URL |
[3] | 中华医学会心血管病学分会介入心脏病学组, 等. 稳定性冠心病诊断与治疗指南[J]. 中华心血管病杂志, 2018, 46(9):680-694 |
[4] |
Lee TM, Chang NC, Lin SZ. 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, 104:298-310.
doi: 10.1016/j.freeradbiomed.2017.01.035 URL |
[5] |
Lin B, Koibuchi N, Hasegawa Y, et al. Glycemic control with empagliflozin, a novel selective SGLT2 inhibitor, ameliorates cardiovascular injury and cognitive dysfunction in obese and type 2 diabetic mice[J]. Cardiovasc Diabetol, 2014, 13:148.
doi: 10.1186/s12933-014-0148-1 URL |
[6] |
Kang S, Verma S, Hassanabad AF, et al. Direct effects of empagliflozin on extracellular matrix remodelling in human cardiac myofibroblasts:novel translational clues to explain EMPA-REG OUTCOME results[J]. Can J Cardiol, 2020, 36(4):543-553.
doi: 10.1016/j.cjca.2019.08.033 URL |
[7] |
Santos-Gallego CG, Requena-Ibanez JA, San Antonio R, et al. Empagliflozin ameliorates adverse left ventricular remodeling in nondiabetic heart failure by enhancing myocardial energetics[J]. J Am Coll Cardiol, 2019, 73(15):1931-1944.
doi: S0735-1097(19)33689-7 pmid: 30999996 |
[8] |
Hallow KM, Helmlinger G, Greasley PJ, et al. Why do SGLT2 inhibitors reduce heart failure hospitalization?A differential volume regulation hypojournal[J]. Diabetes Obes Metab, 2018, 20(3):479-87.
doi: 10.1111/dom.13126 pmid: 29024278 |
[9] |
Horie I, Abiru N, Hongo R, et al. Increased sugar intake as a form of compensatory hyperphagia in patients with type 2 diabetes under dapagliflozin treatment[J]. Diabetes Res Clin Pract, 2018, 135:178-184.
doi: 10.1016/j.diabres.2017.11.016 URL |
[10] |
Garvey WT, Van Gaal L, Leiter LA, et al. Effects of canagliflozin versus glimepiride on adipokines and inflammatory biomarkers in type 2 diabetes[J]. Metabolism, 2018, 85:32-37.
doi: 10.1016/j.metabol.2018.02.002 URL |
[11] |
Hussein AM, Eid EA, Taha M, et al. Comparative study of the effects of GLP1 analog and SGLT2 inhibitor against diabetic cardiomyopathy in type 2 diabetic rats:possible underlying mechanisms[J]. Biomedicines, 2020, 8(3):43.
doi: 10.3390/biomedicines8030043 URL |
[12] |
Lambers Heerspink HJ, de Zeeuw D, et al. Dapagliflozin a glucose-regulating drug with diuretic properties in subjects with type 2 diabetes[J]. Diabetes Obes Metab, 2013, 15(9):853-862.
doi: 10.1111/dom.12127 pmid: 23668478 |
[13] |
Ji L, Ma J, Li H, et al. Dapagliflozin as monotherapy in drug-naive Asian patients with type 2 diabetes mellitus: A randomized, blinded, prospective phase Ⅲ study[J]. Clin Ther, 2014, 36(1):84-100.
doi: 10.1016/j.clinthera.2013.11.002 URL |
[14] |
Zinman B, Wanner C, Lachin JM, et al. Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes[J]. N Engl J Med, 2015, 373:2117-2128.
doi: 10.1056/NEJMoa1504720 URL |
[15] | 穆炳霞, 吴洁. 螺内酯对慢性心衰患者心室重构及心功能的影响[J]. 中国社区医师(医学专业半月刊), 2009, 11(10):20. |
[16] | 李兆, 程功. 钠-葡萄糖共转运蛋白2抑制剂对心室重构的影响[J]. 中国全科医学, 2021, 24(3):267-271 |
[17] |
Singh JSS, Mordi IR, Vickneson K, et al. Dapagliflozin versus placebo on left ventricular remodeling in patients with diabetes and heart failure:the REFORM trial[J]. Diabetes Care, 2020, 43(6):1356-1359.
doi: 10.2337/dc19-2187 URL |
[18] | 包丽雯, 李勇. SGLT2抑制剂恩格列净心血管保护作用及研究——EMPA-HEART Cardiolink 6研究简评[J]. 中国糖尿病杂志, 2019, 27(7):557-560. |
[19] | 邵清淼. SGLT-2抑制剂恩格列净对2型糖尿病大鼠心室重构及线粒体功能的干预研究[D]. 天津:天津医科大学, 2019. |
[20] | 李晨光. 恩格列净对糖尿病心肌氧化应激和纤维化的机制研究[D]. 天津:天津医科大学, 2019. |
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