Considering hyperglycemia and thrombolysis in the Stroke Hyperglycemia Insulin Network Effort (SHINE) trial

Ann N Y Acad Sci. 2012 Sep;1268(1):72-8. doi: 10.1111/j.1749-6632.2012.06731.x.

Abstract

Hyperglycemia is associated with enhanced cortical toxicity and larger infarct volumes following focal cerebral ischemia. Initial blood glucose in acute ischemic stroke patients may also contribute to a differential response to thrombolysis (i.e., administration of tissue plasminogen activator (t-PA)) and affect risk of symptomatic intracerebral hemorrhage (sICH). The Stroke Hyperglycemia Insulin Network Effort (SHINE) study is a phase III single-blinded, randomized control trial comparing an intensive level of glucose control with standard of care glucose control in hyperglycemic stroke patients. In stratifying randomization by treatment with intravenous t-PA, the SHINE trial offers a unique opportunity to evaluate an association between euglycemic control and outcomes from stroke thrombolysis in a prospective, comparative study. We hypothesize that normalization of blood glucose in the acute stroke setting may reduce risk of thrombolysis-induced sICH. With enrollment recently underway, the stratified results from the SHINE trial could substantially influence future treatment decisions for hyperglycemic stroke patients.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Brain Ischemia / blood*
  • Brain Ischemia / complications
  • Brain Ischemia / drug therapy
  • Cerebral Hemorrhage / etiology
  • Cerebral Hemorrhage / prevention & control
  • Diabetes Complications / blood
  • Diabetes Complications / drug therapy
  • Disease Models, Animal
  • Fibrinolytic Agents / therapeutic use
  • Humans
  • Hyperglycemia / drug therapy
  • Hyperglycemia / etiology
  • Hyperglycemia / prevention & control*
  • Infusions, Intravenous
  • Insulin / therapeutic use*
  • NADP / metabolism
  • NADPH Oxidases / metabolism
  • Obesity / complications
  • Recombinant Proteins / therapeutic use
  • Single-Blind Method
  • Superoxides / metabolism
  • Thrombolytic Therapy*
  • Tissue Plasminogen Activator / therapeutic use

Substances

  • Fibrinolytic Agents
  • Insulin
  • Recombinant Proteins
  • Superoxides
  • NADP
  • NADPH Oxidases
  • Tissue Plasminogen Activator