Literature DB >> 16868064

Cortisol response to critical illness: effect of intensive insulin therapy.

Ilse Vanhorebeek1, Robin P Peeters, Sarah Vander Perre, Ivo Jans, Pieter J Wouters, Kristin Skogstrand, Troels K Hansen, Roger Bouillon, Greet Van den Berghe.   

Abstract

CONTEXT: Both excessive and insufficient activation of the hypothalamic-pituitary-adrenal axis in response to critical illness is associated with increased mortality.
OBJECTIVE: The objective of the study was to study the effect of intensive insulin therapy, recently shown to reduce mortality and morbidity of critically ill patients, on the cortisol response to critical illness.
DESIGN: This was a preplanned subanalysis of a large randomized, controlled study measuring serum total cortisol, cortisol-binding globulin, and albumin and calculating free cortisol levels.
SETTING: The study was conducted at a university hospital surgical intensive care unit. PATIENTS: Four hundred fifty-one critically ill patients dependent on intensive care for more than 5 d and 45 control subjects matched for gender, age, height, and weight participated in this study. INTERVENTION: The intervention was strict blood glucose control to normoglycemia with insulin.
RESULTS: Total and calculated free cortisol levels were equally elevated upon admission in both patient groups and thereafter were lower in intensive insulin-treated patients. Lower cortisol levels statistically related to the outcome benefit of intensive insulin therapy. Cortisol-binding globulin levels and structure were affected by critical illness but not insulin therapy, and neither were albumin levels. Administration of hydrocortisone in so-called replacement dose resulted in severalfold higher total and free cortisol levels, indicating that reevaluation of the doses used is warranted.
CONCLUSIONS: Lower serum cortisol levels in critically ill patients receiving intensive insulin therapy statistically related to improved outcome with this intervention. The lower cortisol levels were not related to altered cortisol-binding capacity.

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Year:  2006        PMID: 16868064     DOI: 10.1210/jc.2005-2089

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  14 in total

1.  Association of hyperglycemia, glucocorticoids, and insulin use with morbidity and mortality in the pediatric intensive care unit.

Authors:  Kupper A Wintergerst; Michael B Foster; Janice E Sullivan; Charles R Woods
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2.  Insulin therapy in the intensive care unit should be targeted to maintain blood glucose between 4.4 mmol/l and 6.1 mmol/l.

Authors:  G Van den Berghe
Journal:  Diabetologia       Date:  2007-11-27       Impact factor: 10.122

3.  Tissue-specific difference in the molecular mechanisms for the development of acute insulin resistance after injury.

Authors:  Li Li; LaWanda H Thompson; Ling Zhao; Joseph L Messina
Journal:  Endocrinology       Date:  2008-09-18       Impact factor: 4.736

4.  Reduced nocturnal ACTH-driven cortisol secretion during critical illness.

Authors:  Eva Boonen; Philippe Meersseman; Hilke Vervenne; Geert Meyfroidt; Fabian Guïza; Pieter J Wouters; Johannes D Veldhuis; Greet Van den Berghe
Journal:  Am J Physiol Endocrinol Metab       Date:  2014-02-25       Impact factor: 4.310

Review 5.  Does the type and severity of brain injury predict hypothalamo-pituitary dysfunction? Does post-traumatic hypopituitarism predict worse outcome?

Authors:  M Klose; U Feldt-Rasmussen
Journal:  Pituitary       Date:  2008       Impact factor: 4.107

Review 6.  Critical Care Management of Stress-Induced Hyperglycemia.

Authors:  Ilse Vanhorebeek; Jan Gunst; Greet Van den Berghe
Journal:  Curr Diab Rep       Date:  2018-02-26       Impact factor: 4.810

Review 7.  Adrenal function and dysfunction in critically ill patients.

Authors:  Arno Téblick; Bram Peeters; Lies Langouche; Greet Van den Berghe
Journal:  Nat Rev Endocrinol       Date:  2019-07       Impact factor: 43.330

8.  Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.

Authors:  Mads V Hollegaard; Jakob Grove; Jonas Grauholm; Eskil Kreiner-Møller; Klaus Bønnelykke; Mette Nørgaard; Thomas L Benfield; Bent Nørgaard-Pedersen; Preben B Mortensen; Ole Mors; Henrik T Sørensen; Zitta B Harboe; Anders D Børglum; Ditte Demontis; Torben F Ørntoft; Hans Bisgaard; David M Hougaard
Journal:  BMC Genet       Date:  2011-07-04       Impact factor: 2.797

9.  Reduced cortisol metabolism during critical illness.

Authors:  Eva Boonen; Hilke Vervenne; Philippe Meersseman; Ruth Andrew; Leen Mortier; Peter E Declercq; Yoo-Mee Vanwijngaerden; Isabel Spriet; Pieter J Wouters; Sarah Vander Perre; Lies Langouche; Ilse Vanhorebeek; Brian R Walker; Greet Van den Berghe
Journal:  N Engl J Med       Date:  2013-03-19       Impact factor: 91.245

10.  ACTH and cortisol responses to CRH in acute, subacute, and prolonged critical illness: a randomized, double-blind, placebo-controlled, crossover cohort study.

Authors:  Bram Peeters; Philippe Meersseman; Sarah Vander Perre; Pieter J Wouters; Yves Debaveye; Lies Langouche; Greet Van den Berghe
Journal:  Intensive Care Med       Date:  2018-10-29       Impact factor: 17.440

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