Metabolism - Clinical and Experimental
Volume 57, Issue 5 , Pages 669-671, May 2008

Intensive blood glucose control in acute and prolonged critical illness: endogenous secretion contributes more to plasma insulin than exogenous insulin infusion

  • František Duška

      Affiliations

    • Department of Anesthesia and Critical Care Medicine, The Third Faculty of Medicine, Charles University, 11000 Prague, Czech Republic, EU
    • Corresponding Author InformationCorresponding author.
  • ,
  • Michal Anděl

      Affiliations

    • Department of Internal Medicine II, The Third Faculty of Medicine, Charles University, 11000 Prague, Czech Republic, EU

Received 20 June 2007; accepted 17 January 2008.

Abstract 

We investigated the contribution of impaired insulin secretion (observed as dynamics of C-peptide) and insulin resistance (measured by euglycemic clamps) to glucose dysregulation in 20 critically ill patients after severe trauma during feeding and intensive glucose control with intravenous insulin. Between the fourth and seventh day when insulin sensitivity is lowest, insulin secretion is highest and supranormal despite tight control of blood glucose by exogenous insulin. Afterward, plasma C-peptide decreases together with an improvement in insulin sensitivity. Multiple regression analysis revealed that plasma insulin is determined more by endogenous secretion than insulin infusion, even during the acute phase when exogenous insulin requirements are high.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0026-0495(08)00034-6

doi:10.1016/j.metabol.2008.01.001

Metabolism - Clinical and Experimental
Volume 57, Issue 5 , Pages 669-671, May 2008