de Kruif Martijn D, Lemaire Lucienne C, Giebelen Ida A, Struck Joachim, Morgenthaler Nils G, Papassotiriou Jana, Elliott Peter J, van der Poll Tom
Center for Experimental and Molecular Medicine, Room G2-132, Academic Medical Center, Meibergdreef 9, 1105 Amsterdam, AZ, The Netherlands.
Intensive Care Med. 2008 Mar;34(3):518-22. doi: 10.1007/s00134-007-0955-x. Epub 2007 Dec 14.
Sepsis intervention studies need better patient stratification methods, and one way to realize this is the introduction of stable biomarkers. A set of recently developed novel biomarkers, based upon precursor-fragments of short-lived hormones, was previously shown to be increased during sepsis. However, it is not known whether these biomarkers are influenced by sepsis intervention strategies. Therefore we investigated the markers in a model of human endotoxemia intervened by increasing doses of prednisolone.
Prospective, open-label study in a specialized clinical research unit of a university hospital.
Thirty-two healthy male volunteers.
Subjects received prednisolone orally at doses of 0, 3, 10 or 30 mg (n=8 per group) at 2 h before intravenous injection of Escherichia coli lipopolysaccharide (LPS) (4 ng/kg). Blood samples were drawn during 24 h after LPS injection.
LPS injection caused an increase in levels of midregional pro-adrenomedullin (MR-proADM), midregional pro-atrial natriuretic peptide (MR-proANP), C-terminal pro-arginine-vasopressin (CT-proAVP) and procalcitonin (PCT). Prednisolone caused a dose dependent inhibition of MR-proADM, MR-proANP and CT-proAVP levels.
These results show that a set of novel, highly stable sepsis biomarkers was increased during human endotoxemia and was dose-dependently inhibited by corticosteroid pre-treatment.
脓毒症干预研究需要更好的患者分层方法,实现这一目标的一种方式是引入稳定的生物标志物。先前已证明,一组基于短效激素前体片段的新开发的生物标志物在脓毒症期间会升高。然而,尚不清楚这些生物标志物是否受脓毒症干预策略的影响。因此,我们在通过增加泼尼松龙剂量进行干预的人类内毒素血症模型中研究了这些标志物。
在一家大学医院的专业临床研究单位进行的前瞻性、开放标签研究。
32名健康男性志愿者。
在静脉注射大肠杆菌脂多糖(LPS)(4 ng/kg)前2小时,受试者分别口服0、3、10或30 mg泼尼松龙(每组n = 8)。在注射LPS后的24小时内采集血样。
注射LPS导致中段肾上腺髓质素原(MR-proADM)、中段心钠素原(MR-proANP)、C末端精氨酸加压素原(CT-proAVP)和降钙素原(PCT)水平升高。泼尼松龙对MR-proADM、MR-proANP和CT-proAVP水平有剂量依赖性抑制作用。
这些结果表明,一组新型、高度稳定的脓毒症生物标志物在人类内毒素血症期间升高,并受到皮质类固醇预处理的剂量依赖性抑制。