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过氧化体增殖物激活型受体α/γ激动剂对代谢综合征患者高敏C反应蛋白和基质金属蛋白酶9的影响 被引量:1

The Effect of Peroxisome Proliferator Activated Receptor-α/γ Agonist Intervention on Serum Concentration of High Sensitive C-reactive Protein and Matrix Metalloproteinase-9 in Patients with Metabolic Syndrome
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摘要 目的了解过氧化体增殖物型激活受体α/γ激动剂单用与联用对代谢综合征患者高敏C反应蛋白和基质金属蛋白酶9的影响。方法 256例代谢综合征患者随机分为基础治疗组、非诺贝特组、吡格列酮组、非诺贝特+吡格列酮组。所有患者进行生活方式干预及应用相应药物。在控制血压的基础上,基础治疗组加服安慰剂;非诺贝特组加服非诺贝特0.2 g,每日1次,睡前服;吡格列酮组加服吡格列酮15 mg,每日1次;非诺贝特+吡格列酮组按相同剂量加服上述2种药物。共干预24周。干预前后测定所有患者高敏C反应蛋白和基质金属蛋白酶9的浓度。结果干预前后各组的血清高敏C反应蛋白分别为:非诺贝特组6.32±1.65 mg/L和3.52±1.98 mg/L,吡格列酮组5.85±1.59 mg/L和3.33±1.16 mg/L,非诺贝特+吡格列酮组6.49±1.34 mg/L和2.47±0.91 mg/L;干预前后各组的基质金属蛋白酶9的浓度分别为:非诺贝特组179.3±54.9μg和L/144.9±30.8μg/L,吡格列酮组188.7±62.4μg/L和146.9±27.8μg/L,非诺贝特+吡格列酮组177.5±58.7μg/L和128.8±34.8μg/L。结论单用非诺贝特或吡格列酮干预均可降低代谢综合征患者高敏C反应蛋白和基质金属蛋白酶9浓度,联用较单用降低更明显。 Aim To explore the effect of peroxisome proliferator activated receptors-α/γ(PPAR-α/γ) agonist intervention alone or in combination on serum concentration of high sensitive C-reactive protein(hs-CRP) and matrix metalloproteinase-9(MMP-9) in patients with metabolic syndrome. Methods 256 patients with metabolic syndrom were randomly assigned into basic treatment group,fenofibrate group,pioglitazone group,and fenofibrate+pioglitazone group.All patients received lifestyle interventions and medications to control blood pressure.Additionally,patients in the B group received placebo.Patients in the fenofibrate group received fenofibrate 0.2 g once a day at night.Patients in the pioglitazone group received pioglitazone 15 mg once a day.Patients in the fenofibrate+pioglitazone group received both fenofibrate and pioglitazone as described above.The intervention lasted for 24 weeks.All patients' serum concentration of hs-CRP and MMP-9 were checked pre and post intervention. Results Patients' serum concentration of hs-CRP pre and post intervention in each group were 6.32±1.65 mg/L and 3.52±1.98 mg/L in the fenofibrate group,5.85±1.59 mg/L and 3.33±1.16 mg/L in the pioglitazone group,and 6.49±1.34 mg/L and 2.47±0.91 mg/L in the fenofibrate +pioglitazone group respectively.Patients' serum concentration of MMP-9 pre and post intervention in each group were 179.3±54.9 μg/L and 144.9±30.8 μg/L in the fenofibrate group,188.7±62.4 μg/L and 146.9±27.8 μg/L in the pioglitazone group,and 177.5±58.7 μg/L and 128.8±34.8 μg/L in the fenofibrate+pioglitazone group respectively.Conclusions Fenofibrate or pioglitazone intervention alone can reduce serum concentration of hs-CRP and MMP-9 in patients with metabolic syndrome.A combined use of fenofibrate and pioglitazone was more effective than single intervention with fenofibrate or pioglitazone.
出处 《中国动脉硬化杂志》 CAS CSCD 北大核心 2011年第12期1011-1014,共4页 Chinese Journal of Arteriosclerosis
关键词 代谢综合征 过氧化体增殖物激活型受体α/γ激动剂 高敏C反应蛋白 基质金属蛋白酶9 Metabolic Syndrome Peroxisome Proliferator Activated Receptors-α/γ Agonists High Sensitive C-reactive Protein Matrix Metalloproteinase-9
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参考文献8

  • 1Festa AD, Agostino R Jr, Howard G, et al. Chronic sub- clinical inflammation as part of the insulin resistance syn- drome : The insulin resistance atherosclerosis study (IRAS) [J]. Circulation, 2000, 102 (1):42-47.
  • 2Hanefeld M, Marx N, Pfutzner A, et al. Anti-inflammatory effects of pioglitazone and/or simvastatin in high cardiovas- cular risk patients with elevated high sensitivity C-reactive protein: the PIOSTAT study [ J ]. J Am Coil Cardiol, 2007, 49 (3) : 290-297.
  • 3Keech A, Simes RJ, Barter P, et al. Effects of long term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus ( the FIELD study) : Random- ized controlled trial [ J ]. Lancet, 2005, 366 (9500) : 1 849-861.
  • 4Mazzone T, Meyer PM, Feinsein SB, et al. Effect of piogl- itazone compared with glimepiride on carotid intima-media thickness in type 2 diabetes: a randomized trial [ J ]. JA- MA, 2006, 296(21): 2 572-581.
  • 5郑甲林,杨丽霞,王先梅,严睿,刘力,齐峰,任丽.64层螺旋CT联合高敏C反应蛋白及基质金属蛋白酶9检测急性冠脉综合征患者易损斑块的相关研究[J].中国实用内科杂志,2009,29(11):1021-1023. 被引量:6
  • 6Endres M. Statins. Potential new indieations in inflammato- ry conditions [ J ]. Atheroscler Suppl, 2006, 7 ( 1 ) : 31-35.
  • 7Yoshimoto T, Naruse M, Shizume H, et al. Vaseulo-pro- tective effects of insulin sensitizing agent pioglitazone in neointimal thickening and hypertensive vascular hypertro- phy[J]. Atherosclerosis, 1999, 145 (2): 333-340.
  • 8Martens FM, Visseren FL, Lemay J, et al. Metabolic and additional vascular effects of thiazolidinediones [ J ]. Drugs, 2002, 62 (10) : 1 463-480.

二级参考文献5

  • 1Hausleiter J, Meyer T,Hadamitzky M, et al. Non-invasive coronary computed tomographic angiography for patients with suspected coronary artery disease: the Coronary Angiography by Computed Tomography with the Use of a Submillimeter resolution(CACTUS) [ J ]. Eur Heart J, 2007,28 ( 24 ) :3034 - 3041.
  • 2Choi B J, Kang DK, Tahk S J, et al. Comparison of 64-slice multiderector computed tomography with spectral analysis of intravascular ultrasound backscatter signals for characterizations of noncalcified coronary .arterial plaques[ J]. Am J Cardiol,2008,102( 8 ) :988 - 993.
  • 3Rasouli ML, Shavelle DM, French WJ, et al. Assessment of coronary plaque morphology by contrast-enhanced computed tomographic angiography : comparison with intravascular ultrasound [ J ]. Coron Artery Dis, 2006,17 ( 4 ) :359 - 364.
  • 4Kopp AF, Schroeder S, Baumbach A, et al. Noninvasive characterization of coronary lesion morphology and composition by multislice CT: first results in comparison with intracoronary ultrasound [ J]. Eur Radiol,2001,11 (9) :1607 - 1511.
  • 5Schroeder S, Kuettner A, Wojak T, et al. Non-invasive evaluation of atherosclerosis with contrast enhanced 16 slice spiral computed tomography:results of ex vivo investigation [ J ]. Heart, 2004,90 (12) : 1471 - 1475.

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