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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >The effect of early treatment by cerivastatin on the serum level of C-reactive protein, interleukin-6, and interleukin-8 in the patients with unstable angina and non-Q-wave myocardial infarction
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The effect of early treatment by cerivastatin on the serum level of C-reactive protein, interleukin-6, and interleukin-8 in the patients with unstable angina and non-Q-wave myocardial infarction

机译:西瓦伐他汀早期治疗对不稳定型心绞痛和非Q波心肌梗死患者血清C反应蛋白,白细胞介素6和白细胞介素8的影响

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摘要

The aim of our study was to evaluate whether a single dose of cerivastatin at the time of admission of patients with unstable angina pectoris (USP) or non-Q-wave myocardial infarction (NQMI) can influence the serum level of C-reactive protein (CRP), intrleukin-6 (IL-6) and intrleukin-8 (IL-8) 24 h later. Forty-four patients with rest chest pain and subendocardial ischemia on ECG were randomized to receive cerivastatin 0.3 mg at the time of admission (group C+) to standard therapy or to remain just on standard therapy (group C-). Blood samples for determination of troponin I (TI), CRP, IL-6 and IL-8 were collected at admission (entry level) and 24 h later (final level). Patients with non-physiological baseline levels of TI, as well as patients with progression to Q wave MI were excluded. All baseline, clinical and demographic data and final values of TI were comparable in the two groups. In patients treated with cerivastatin (group C+, n = 13) we observed decrease in the CRP level (-6.73 ± 3.93 mg/L); on the other hand, in group C- (n = 17) the CRP level increased (+ 7.92 ± 2.77 mg/L, p = 0.004). Similar differences were observed also in IL-6: in group C+ the level was significantly reduced as compared with the increase in group C-(-0.76 ± 0.52 vs. 4.58 ± 1.49 ng/L, p = 0.005). The level of IL-8 was not affected. Our results suggest that early treatment with cerivastatin can decrease the serum level of CRP and IL-6 patients with UAP/NQMI; this might positively influence their prognosis. Nevertheless, further studies are needed to support this hypothesis.
机译:我们研究的目的是评估不稳定型心绞痛(USP)或非Q波心肌梗死(NQMI)患者入院时单剂量西立伐他汀是否会影响C反应蛋白的血清水平( CRP),白介素6(IL-6)和白介素8(IL-8)在24小时后。在入院时(C +组),有44例因心电图休息胸痛和心内膜下局部缺血的患者被随机分配接受0.3 mg西立伐他汀(标准治疗)或仅接受标准治疗(C-组)。在入院(进入水平)和24小时后(最终水平)收集用于测定肌钙蛋白I(TI),CRP,IL-6和IL-8的血样。 TI的非生理基线水平的患者以及进展为Q波MI的患者均被排除在外。两组的所有基线,临床和人口统计学数据以及TI的最终值均相当。在接受西立伐他汀治疗的患者中(C +组,n = 13),我们观察到CRP水平降低(-6.73±3.93 mg / L);另一方面,在C-组(n = 17)中,CRP水平升高(+ 7.92±2.77 mg / L,p = 0.004)。在IL-6中也观察到类似的差异:与C-组相比,C +组的水平明显降低(-0.76±0.52 vs. 4.58±1.49 ng / L,p = 0.005)。 IL-8的水平不受影响。我们的结果表明,早期使用西立伐他汀可以降低UAP / NQMI患者的CRP和IL-6血清水平;这可能会对他们的预后产生积极影响。然而,需要进一步的研究来支持这一假设。

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