Clinical Focus ›› 2021, Vol. 36 ›› Issue (9): 778-781.doi: 10.3969/j.issn.1004-583X.2021.09.002
Previous Articles Next Articles
Guo Jiamin1,2, Zhang Guangming1(), Yang Jing1, Gu Guoqiang1, Lu Rui1, Xing Hanghang1, Cui Wei1
Received:
2020-11-16
Online:
2021-09-20
Published:
2021-10-05
Contact:
Zhang Guangming
E-mail:zhangguangming76@sina.com
CLC Number:
Guo Jiamin, Zhang Guangming, Yang Jing, Gu Guoqiang, Lu Rui, Xing Hanghang, Cui Wei. Effects of ticagrelor and clopidogrel on vascular endothelial function of patients with coronary heart disease[J]. Clinical Focus, 2021, 36(9): 778-781.
Add to citation manager EndNote|Ris|BibTeX
URL: https://huicui.hebmu.edu.cn/EN/10.3969/j.issn.1004-583X.2021.09.002
项目 | 替格瑞洛组(n=40) | 氯吡格雷组(n=40) | Z/χ2值 | P值 |
---|---|---|---|---|
男[例(%)] | 27(67.5) | 32(80.0) | 1.614 | 0.204 |
年龄(岁) | 60.0(53.5,65.0) | 58.0(49.0,67.0) | -0.058 | 0.954 |
体重指数(kg/m2) | 26.0(24.1,27.7) | 26.7(23.1,27.8) | -0.433 | 0.665 |
吸烟史[例(%)] | 15(37.50) | 15(37.50) | 0.000 | 0.000 |
高血压[例(%)] | 26(65.00) | 20(50.00) | 1.841 | 0.175 |
糖尿病[例(%)] | 13(32.50) | 7(17.50) | 2.400 | 0.121 |
高脂血症[例(%)] | 10(25.00) | 15(37.50) | 1.455 | 0.228 |
卒中史[例(%)] | 2(5.00) | 4(10.00) | 0.721 | 0.396 |
hs-CRP(mg/L) | 1.5(0.9,3.9) | 1.5(0.9,3.9) | -0.645 | 0.519 |
UA(mmol/L) | 293.0(266.0,366.5) | 309.0(255.0,403.0) | -0.221 | 0.825 |
Cr(μmol/L) | 66.0(58.8,75.6) | 70.0(63.3,80.0) | -1.530 | 0.126 |
TG(mmol/L) | 3.6(3.2,4.3) | 4.0(3.7,4.5) | -1.954 | 0.051 |
LDL-C(mmol/L) | 2.2(1.8,3.1) | 2.7(2.2,2.9) | -1.720 | 0.085 |
FBG(mmol/L) | 5.2(4.6,6.5) | 5.2(4.7,5.8) | -0.092 | 0.927 |
TnI(ng/ml) | <0.01(<0.01,0.2) | <0.01(<0.01,0.1) | -1.740 | 0.082 |
BNP(pg/ml) | 40.4(10.7,128.3) | 25.5(13.8,75.8) | -1.202 | 0.229 |
LVEF(%) | 62.0(61.3,63.7) | 62.0(60.8,63.3) | -0.779 | 0.436 |
单支病变[例(%)] | 15(37.50) | 13(32.50) | 0.000 | 0.000 |
双支病变[例(%)] | 15(37.50) | 12(30.00) | 0.000 | 0.000 |
三支病变[例(%)] | 10(25.00) | 15(37.50) | 1.476 | 0.478 |
ACEI/ARB[例(%)] | 4(10.00) | 6(15.00) | 0.457 | 0.499 |
β受体阻滞剂[例(%)] | 12(30.00) | 16(40.00) | 0.879 | 0.348 |
钙离子拮抗剂[例(%)] | 11(27.50) | 14(35.00) | 0.524 | 0.469 |
项目 | 替格瑞洛组(n=40) | 氯吡格雷组(n=40) | Z/χ2值 | P值 |
---|---|---|---|---|
男[例(%)] | 27(67.5) | 32(80.0) | 1.614 | 0.204 |
年龄(岁) | 60.0(53.5,65.0) | 58.0(49.0,67.0) | -0.058 | 0.954 |
体重指数(kg/m2) | 26.0(24.1,27.7) | 26.7(23.1,27.8) | -0.433 | 0.665 |
吸烟史[例(%)] | 15(37.50) | 15(37.50) | 0.000 | 0.000 |
高血压[例(%)] | 26(65.00) | 20(50.00) | 1.841 | 0.175 |
糖尿病[例(%)] | 13(32.50) | 7(17.50) | 2.400 | 0.121 |
高脂血症[例(%)] | 10(25.00) | 15(37.50) | 1.455 | 0.228 |
卒中史[例(%)] | 2(5.00) | 4(10.00) | 0.721 | 0.396 |
hs-CRP(mg/L) | 1.5(0.9,3.9) | 1.5(0.9,3.9) | -0.645 | 0.519 |
UA(mmol/L) | 293.0(266.0,366.5) | 309.0(255.0,403.0) | -0.221 | 0.825 |
Cr(μmol/L) | 66.0(58.8,75.6) | 70.0(63.3,80.0) | -1.530 | 0.126 |
TG(mmol/L) | 3.6(3.2,4.3) | 4.0(3.7,4.5) | -1.954 | 0.051 |
LDL-C(mmol/L) | 2.2(1.8,3.1) | 2.7(2.2,2.9) | -1.720 | 0.085 |
FBG(mmol/L) | 5.2(4.6,6.5) | 5.2(4.7,5.8) | -0.092 | 0.927 |
TnI(ng/ml) | <0.01(<0.01,0.2) | <0.01(<0.01,0.1) | -1.740 | 0.082 |
BNP(pg/ml) | 40.4(10.7,128.3) | 25.5(13.8,75.8) | -1.202 | 0.229 |
LVEF(%) | 62.0(61.3,63.7) | 62.0(60.8,63.3) | -0.779 | 0.436 |
单支病变[例(%)] | 15(37.50) | 13(32.50) | 0.000 | 0.000 |
双支病变[例(%)] | 15(37.50) | 12(30.00) | 0.000 | 0.000 |
三支病变[例(%)] | 10(25.00) | 15(37.50) | 1.476 | 0.478 |
ACEI/ARB[例(%)] | 4(10.00) | 6(15.00) | 0.457 | 0.499 |
β受体阻滞剂[例(%)] | 12(30.00) | 16(40.00) | 0.879 | 0.348 |
钙离子拮抗剂[例(%)] | 11(27.50) | 14(35.00) | 0.524 | 0.469 |
组别 | 例数 | NO(μmol/L) | ET-1(pg/ml) | ||
---|---|---|---|---|---|
治疗前 | 治疗后 | 治疗前 | 治疗后 | ||
替格瑞洛组 | 40 | 2.89(2.57,4.39) | 5.39(4.63,8.41)* | 211.17(188.23,265.59) | 187.52(168.95,239.01)* |
氯吡格雷组 | 40 | 2.96(2.45,4.49) | 4.14(3.24,5.37)* | 257.32(186.24,413.89) | 243.76(184.17,398.78)* |
Z值 | -0.144 | -3.536 | -1.099 | -2.408 | |
P值 | 0.885 | <0.001 | 0.272 | 0.016 |
组别 | 例数 | NO(μmol/L) | ET-1(pg/ml) | ||
---|---|---|---|---|---|
治疗前 | 治疗后 | 治疗前 | 治疗后 | ||
替格瑞洛组 | 40 | 2.89(2.57,4.39) | 5.39(4.63,8.41)* | 211.17(188.23,265.59) | 187.52(168.95,239.01)* |
氯吡格雷组 | 40 | 2.96(2.45,4.49) | 4.14(3.24,5.37)* | 257.32(186.24,413.89) | 243.76(184.17,398.78)* |
Z值 | -0.144 | -3.536 | -1.099 | -2.408 | |
P值 | 0.885 | <0.001 | 0.272 | 0.016 |
[1] |
Gimbrone MA Jr. Vascular endothelium: Nature's blood-compatible container[J]. Ann N Y Acad Sci, 1987, 516:5-11.
doi: 10.1111/nyas.1987.516.issue-1 URL |
[2] |
Houston M. The role of noninvasive cardiovascular testing, applied clinical nutrition and nutritional supplements in the prevention and treatment of coronary heart disease[J]. Ther Adv Cardiovasc Dis, 2018, 12(3):85-108.
doi: 10.1177/1753944717743920 pmid: 29316855 |
[3] | 芦娜, 王宏宇. 内皮功能障碍的生物标志物[J]. 心血管病学进展, 2010, (5):666-669. |
[4] |
Campo G, Vieceli Dalla Sega F, Pavasini R, et al. Biological effects of ticagrelor over clopidogrel in patients with stable coronary artery disease and chronic obstructive pulmonary disease[J]. Thromb Haemost, 2017, 117(6):1208-1216.
doi: 10.1160/TH16-12-0973 URL |
[5] |
Alemayehu M, Kim RB, Lavi R, et al. Effect of ticagrelor versus clopidogrel on vascular reactivity[J]. J Am Coll Cardiol, 2017, 69(17):2246-2248.
doi: S0735-1097(17)35973-9 pmid: 28449783 |
[6] |
Heitzer T, Rudolph V, Schwedhelm E, et al. Clopidogrel improves systemic endothelial nitric oxide bioavailability in patients with coronary artery disease: evidence for antioxidant and antiinflammatory effects[J]. Arterioscler Thromb Vasc Biol, 2006, 26(7):1648-1652.
pmid: 16675725 |
[7] |
Warnholtz A, Ostad MA, Velich N, et al. A single loading dose of clopidogrel causes dose-dependent improvement of endothelial dysfunction in patients with stable coronary artery disease: Results of a double-blind, randomized study[J]. Atherosclerosis, 2008, 196(2):689-695.
pmid: 17214996 |
[8] | 中国医师协会急诊医师分会, 国家卫健委能力建设与继续教育中心急诊学专家委员会, 中国医疗保健国际交流促进会急诊急救分会. 急性冠脉综合征急诊快速诊疗指南(2019)[J]. 临床急诊杂志, 2019, 20(4):253-262. |
[9] |
Bonetti PO, Lerman LO, Lerman A. Endothelial dysfunction: A marker of atherosclerotic risk[J]. Arterioscler Thromb Vasc Biol, 2003, 23(2):168-175.
pmid: 12588755 |
[10] | Davignon J, Ganz P. Role of endothelial dysfunction in atherosclerosis[J]. Circulation, 2004, 109(23 Suppl 1): III27-32. |
[11] |
Vita JA, Keaney JF Jr. Endothelial function: A barometer for cardiovascular risk[J]. Circulation, 2002, 106(6):640-642.
doi: 10.1161/01.CIR.0000028581.07992.56 URL |
[12] |
Jakubowski A, Chlopicki S, Olszanecki R, et al. Endothelial action of thienopyridines and thienopyrimidinones in the isolated guinea pig heart[J]. Prostaglandins Leukot Essent Fatty Acids, 2005, 72(2):139-145.
doi: 10.1016/j.plefa.2004.10.011 URL |
[13] |
Graff J, Harder S, Wahl O, et al. Anti-inflammatory effects of clopidogrel intake in renal transplant patients: Effects on platelet-leukocyte interactions, platelet CD40 ligand expression, and proinflammatory biomarkers[J]. Clin Pharmacol Ther, 2005, 78(5):468-476.
doi: 10.1016/j.clpt.2005.08.002 URL |
[14] |
Jeong HS, Hong SJ, Cho SA, et al. Comparison of ticagrelor versus prasugrel for inflammation, vascular function, and circulating endothelial progenitor cells in diabetic patients with non-ST-segment elevation acute coronary syndrome requiring coronary stenting: A prospective, randomized, crossover trial[J]. JACC Cardiovasc Interv, 2017, 10(16):1646-1658.
doi: 10.1016/j.jcin.2017.05.064 URL |
[15] |
Kim HK, Jeong MH, Lim KS, et al. Effects of ticagrelor on neointimal hyperplasia and endothelial function, compared with clopidogrel and prasugrel, in a porcine coronary stent restenosis model[J]. Int J Cardiol, 2017, 240(8):326-331.
doi: 10.1016/j.ijcard.2017.04.108 URL |
[16] |
Armstrong D, Summers C, Ewart L, et al. Characterization of the adenosine pharmacology of ticagrelor reveals therapeutically relevant inhibition of equilibrative nucleoside transporter 1[J]. J Cardiovasc Pharmacol Ther, 2014, 19(2):209-219.
doi: 10.1177/1074248413511693 URL |
[17] |
Fredholm BB. Adenosine. An endogenous distress signal, modulates tissue damage and repair[J]. Cell Death Differ, 2007, 14(7):1315-1323.
pmid: 17396131 |
[18] |
Wang X, Han X, Li M, et al. Ticagrelor protects against Ang II-induced endothelial dysfunction by alleviating endoplasmic reticulum stress[J]. Microvasc Res, 2018, 119(9):98-104.
doi: 10.1016/j.mvr.2018.05.006 URL |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||