Novack Victor, Eisinger Miruna, Frenkel Amit, Terblanche Marius, Adhikari Neill K J, Douvdevani Amos, Amichay Doron, Almog Yaniv
Department of Medicine, Faculty of Health Sciences, Soroka University Medical Center, Ben Gurion University of the Negev, Beersheba, Israel.
Intensive Care Med. 2009 Jul;35(7):1255-60. doi: 10.1007/s00134-009-1429-0. Epub 2009 Feb 11.
To determine if statin therapy reduces the incidence of severe sepsis and the levels of inflammatory cytokines in patients with acute bacterial infection.
Double-blind placebo controlled randomized clinical trial.
Department of medicine and medical intensive care unit in a tertiary university medical center.
A total of 83 patients with suspected or documented bacterial infection were enrolled. We randomly assigned 42 patients to receive 40 mg of simvastatin orally, followed by 20 mg of simvastatin, and 41 to receive matching placebo.
The study was prematurely terminated due to slow recruitment rate. Here we report the analysis of the secondary outcome: change in cytokines levels at 72 h. Both groups were evenly matched in terms of co-morbidity and severity of illness on admission. Four of the 83 patients enrolled developed severe sepsis, two in each group. No difference was observed in other clinical variables and there were no mortalities. Cytokine levels were randomly assessed in 40 patients (20 in each group). Both TNF-alpha and IL-6 levels were significantly reduced in the simvastatin group (p = 0.02 and p = 0.02, respectively), while no such difference was observed in the placebo group (p = 0.35 and 0.39, respectively).
Statin therapy may be associated with a reduction in the levels of inflammatory cytokines in patients with acute bacterial infections. Large controlled trials will determine if this reduction will translate into a clinical benefit.
确定他汀类药物治疗是否能降低急性细菌感染患者严重脓毒症的发生率及炎症细胞因子水平。
双盲安慰剂对照随机临床试验。
一所三级大学医学中心的内科及医学重症监护病房。
共纳入83例疑似或确诊细菌感染的患者。我们将42例患者随机分配至口服40mg辛伐他汀组,随后服用20mg辛伐他汀,41例患者服用匹配的安慰剂。
由于入组率低,该研究提前终止。在此我们报告次要结局分析:72小时时细胞因子水平的变化。两组在入院时的合并症及疾病严重程度方面均衡匹配。83例入组患者中有4例发生严重脓毒症,每组各2例。在其他临床变量方面未观察到差异,且无死亡病例。对40例患者(每组20例)随机评估细胞因子水平。辛伐他汀组的肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)水平均显著降低(分别为p = 0.02和p = 0.02),而安慰剂组未观察到此类差异(分别为p = 0.35和0.39)。
他汀类药物治疗可能与急性细菌感染患者炎症细胞因子水平降低有关。大型对照试验将确定这种降低是否会转化为临床益处。