Arlt Wiebke, Hammer Fabian, Sanning Petra, Butcher Stephen K, Lord Janet M, Allolio Bruno, Annane Djillali, Stewart Paul M
Medical Research Council Senior Clinical Fellow, Division of Medical Sciences, University of Birmingham, Institute of Biomedical Research, Room 233, Birmingham B15 2TT, United Kingdom.
J Clin Endocrinol Metab. 2006 Jul;91(7):2548-54. doi: 10.1210/jc.2005-2258. Epub 2006 Apr 11.
Dehydroepiandrosterone (DHEA) replacement in sepsis has been advocated because of the sepsis-associated decrease in serum DHEA sulfate (DHEAS). However, experimental sepsis in rodents leads to down-regulation of DHEA sulfotransferase, which inactivates DHEA to DHEAS, theoretically resulting in higher DHEA levels.
The objective of the study was to test whether serum DHEA and DHEAS are dissociated in septic shock and to determine their association with circulating cortisol in the context of severity of disease and mortality.
DESIGN, SETTING, AND PARTICIPANTS: This was a cross-sectional study consisting of 181 patients with septic shock, 31 patients with acute trauma, and 60 healthy controls.
Serum cortisol, DHEA, and DHEAS were measured before and 60 min after ACTH stimulation.
Serum cortisol was increased and DHEAS was decreased in both septic shock and trauma patients (all P < 0.001). However, compared with healthy controls, DHEA was significantly increased in sepsis but decreased after trauma (all P < 0.001). In sepsis, neither cortisol nor DHEA increased significantly after ACTH. Most severely ill patients had higher cortisol (P = 0.069) and lower DHEA (P = 0.076) and a significantly higher cortisol to DHEA ratio (P = 0.004). Similarly, the cortisol to DHEA ratio was significantly increased in nonsurvivors of septic shock (P = 0.026), whereas survivors did not differ from controls (P = 0.322).
The observed dissociation of DHEA and DHEAS in septic shock contradicts the previous concept of sepsis-associated DHEA deficiency. Increased DHEA levels may maintain the balance between glucocorticoid- and DHEA-mediated immune and vascular effects. However, most severe disease and mortality is associated with an increased cortisol to DHEA ratio, which may represent a novel prognostic marker in septic shock.
由于脓毒症相关的血清硫酸脱氢表雄酮(DHEAS)水平降低,有人主张在脓毒症中补充脱氢表雄酮(DHEA)。然而,啮齿动物的实验性脓毒症会导致DHEA硫酸转移酶下调,该酶可使DHEA失活转化为DHEAS,理论上会导致DHEA水平升高。
本研究的目的是检测脓毒性休克患者血清DHEA和DHEAS是否解离,并在疾病严重程度和死亡率的背景下确定它们与循环皮质醇的关系。
设计、地点和参与者:这是一项横断面研究,包括181例脓毒性休克患者、31例急性创伤患者和60名健康对照者。
在促肾上腺皮质激素(ACTH)刺激前和刺激后60分钟测量血清皮质醇、DHEA和DHEAS。
脓毒性休克患者和创伤患者的血清皮质醇均升高,DHEAS均降低(所有P<0.001)。然而,与健康对照者相比,脓毒症患者的DHEA显著升高,而创伤患者的DHEA降低(所有P<0.001)。在脓毒症中,ACTH刺激后皮质醇和DHEA均未显著升高。病情最严重的患者皮质醇水平较高(P=0.069),DHEA水平较低(P=0.076),皮质醇与DHEA的比值显著更高(P=0.004)。同样,脓毒性休克非幸存者的皮质醇与DHEA比值显著升高(P=0.026),而幸存者与对照者无差异(P=0.322)。
在脓毒性休克中观察到的DHEA和DHEAS解离与先前关于脓毒症相关DHEA缺乏的概念相矛盾。DHEA水平升高可能维持糖皮质激素和DHEA介导的免疫及血管效应之间的平衡。然而,最严重的疾病和死亡率与皮质醇与DHEA比值升高有关,这可能是脓毒性休克的一种新的预后标志物。