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首页> 外文期刊>Calcified tissue international. >No effect of rosuvastatin in the zoledronate-induced acute-phase response.
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No effect of rosuvastatin in the zoledronate-induced acute-phase response.

机译:瑞舒伐他汀在唑来膦酸盐诱导的急性期反应中无作用。

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摘要

The acute-phase response (APR) is frequently observed in patients treated with intravenous (iv) zoledronate (ZOL). We investigated whether a short course of rosuvastatin (ROSU) could attenuate the ZOL--induced APR through blocking the mevalonate pathway at a proximal level. Twenty-eight osteoporotic postmenopausal women with no prior bisphosphonate use (mean age 65.3 +/- 1.9 years) were subjected to ZOL iv infusion. Patients were randomly assigned into either a ROSU+ group (n = 12), which received ROSU 10 mg/day starting 5 days before the infusion of ZOL for a total period of 11 days, or a ROSU- group (n = 16), which did not receive ROSU. The visual analog pain scale (VAS) for musculoskeletal symptoms and body temperature was used to define clinically APR. In addition, white blood cell (WBC) count, leukocytic subpopulations, and C-reactive protein (CRP) were obtained before and 48 h following the infusion. Seven (58.3%) patients in the ROSU+ group and 13 (81.3%) in the ROSU- group experienced APR (P = not significant). No difference was found in fever and VAS measurements. CRP and granulocytes increased significantly in both groups; WBC count increased, while lymphocytes and eosinophils decreased significantly only in the ROSU- group. In a post hoc analysis of only patients with an APR, all laboratory parameters exhibited a similar significant change solely within the ROSU- group. In conclusion, our data suggest that a short course of ROS at this dose cannot prevent the ZOL-induced APR among osteoporotic women. Milder changes in acute-phase laboratory parameters in ROSU+ patients suggest that studies with higher doses may be warranted.
机译:在接受静脉注射(iv)唑来膦酸盐(ZOL)治疗的患者中经常观察到急性期反应(APR)。我们研究了短程的瑞舒伐他汀(ROSU)是否可以通过在近端水平阻断甲羟戊酸途径来减弱ZOL诱导的APR。未曾使用过双膦酸盐的28名绝经后绝经后骨质疏松妇女(平均年龄65.3 +/- 1.9岁)接受了ZOL iv输注。将患者随机分为ROSU +组(n = 12)和ROSU-组(n = 16),ROSU +组(n = 12)在输注ZOL前5天开始接受ROSU,每天10 mg,共11天。没有收到ROSU。用于肌肉骨骼症状和体温的视觉模拟疼痛量表(VAS)用于定义临床APR。另外,在输注之前和输注48小时后获得白细胞(WBC)计数,白细胞亚群和C反应蛋白(CRP)。 ROSU +组中有7名(58.3%)患者和ROSU-组中有13名(81.3%)患者发生了APR(P =不显着)。在发烧和VAS测量中未发现差异。两组的CRP和粒细胞显着增加;仅在ROSU-组中,白细胞计数增加,而淋巴细胞和嗜酸性粒细胞显着减少。在仅对APR患者进行事后分析中,仅在ROSU-组内,所有实验室参数均表现出相似的显着变化。总之,我们的数据表明,在此剂量下短时间的ROS不能预防ZOL诱导的骨质疏松妇女的APR。 ROSU +患者急性期实验室参数出现轻度变化,提示可能需要进行更高剂量的研究。

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