Context: Corticosteroid-binding globulin (CBG) and albumin transport circulating cortisol. Cleavage of high-affinity CBG (haCBG) by neutrophil elastase at inflammatory sites causes cortisol release into tissues, facilitating immunomodulatory effects. Objective: To determine whether depletion of haCBG is related to mortality in septic shock. Design: A single-center prospective observational cohort study of patients recruited with critical illness or septic shock, using serum samples collected at 0, 8, 24, 48 and 72 hours. Serum total and haCBG, and total and free cortisol were assayed directly. Glucocorticoid treatment was an exclusion criterion. Mortality was assessed at 28 days from Intensive Care Unit admission. Results: Thirty septic shock (SS) and 42 nonseptic critical illness (CI) patients provided 195 serum samples. SS/CI patients had lower total CBG, haCBG and low-affinity CBG (laCBG) than controls. Total CBG and haCBG were significantly lower in septic shock patients who died than in those that survived (P < 0.009, P = 0.021, respectively). Total and free cortisol were higher in septic than nonseptic individuals. Free/total cortisol fractions were higher in those with low haCBG as observed in septic shock. However, cortisol levels were not associated with mortality. Albumin levels fell in sepsis but were not related to mortality. Conclusions: Low circulating haCBG concentrations are associated with mortality in septic shock. These results are consistent with an important physiological role for haCBG in cortisol tissue delivery in septic shock.

Additional Metadata
Keywords CBG, corticosteroid-binding globulin, cortisol, mortality, septic shock
Persistent URL dx.doi.org/10.1111/cen.13844, hdl.handle.net/1765/110551
Journal Clinical Endocrinology
Citation
Meyer, E.J. (Emily J.), Nenke, M.A. (Marni A.), Rankin, W. (Wayne), Lewis, J.G, Konings, E.E.M, Slager, M.A, … Torpy, D.J. (David J.). (2018). Total and high-affinity corticosteroid-binding globulin depletion in septic shock is associated with mortality. Clinical Endocrinology. doi:10.1111/cen.13844