Hyperglycemia and antibody titres against heat shock protein 27 in traumatic brain injury patients on parenteral nutrition
Authors
Abstract:
Objective(s):Hyperglycemia worsens the neuronal death induced by cerebral ischemia. Previous studies demonstrated that diabetic hyperglycemia suppressed the expression of heat shock protein 70 and 60 (HSP70 and 60) in the liver. IgG antibody titres against heat shock protein 27 (anti HSP27) were measured to determine whether hyperglycemia exacerbates ischemic brain damage by suppressing the expression of heat shock protein 27 (HSP27) in the brain. Materials and Methods: A randomized controlled study of traumatic brain injury ICU patients treated either by intensive insulin treatment (IIT) or by conventional glucose control (CGC) was conducted. Patients received at least 50% of their estimated daily energy requirements parenterally. Serum anti HSP27 antibody concentration was assessed at baseline, day 7 and day 14. Results: Twenty-six out of 29 patients (n=13 in each group) completed the study. At baseline, there were no differences between the two groups. On day 14, there was a significant reduction in anti HSP27 titre concentration in the IIT compared to the GCG group (0.47±0.27 mg/dl vs 0.60±0.15 mg/dl, P=0.03). Conclusion: In this study, intensive control of traumatic brain injury patients on parenteral nutrition reduced anti HSP27 titre, possibly suggesting a reduction in stress.
similar resources
hyperglycemia and antibody titres against heat shock protein 27 in traumatic brain injury patients on parenteral nutrition
objective(s):hyperglycemia worsens the neuronal death induced by cerebral ischemia. previous studies demonstrated that diabetic hyperglycemia suppressed the expression of heat shock protein 70 and 60 (hsp70 and 60) in the liver. igg antibody titres against heat shock protein 27 (anti hsp27) were measured to determine whether hyperglycemia exacerbates ischemic brain damage by suppressing the exp...
full textO 27: Traumatic Brain Injury and Inflammation
Traumatic brain injury (TBI) is a significant public health concern in our country, because of placing in top three most common causes of death and substantial direct and indirect costs to society. The incidence of TBI in our country is 1.7 times of international incidence. Traumatic brain injury induced by primary and secondary mechanisms that give rise to death and neurologic morbidity in pat...
full textTraumatic brain injury and hyperglycemia
We read with great interest the recent study by Shi et al [1] published in the Oncotarget. The management of modifiable risk factors in traumatic brain injury victims has a main role in the patients outcome and a inappropriate treatment is followed by a worse prognosis. Knowledge about the mechanism of hyperglycemia, comorbidities, potential causes, effects and associated factors can improve th...
full textShock Protein 27 Mutant Protects Against Ischemia/Reperfusion Injury in a Transgenic Overexpression of Wild-Type Heat Shock Protein 27 and a Nonphosphorylatable Heat
John M. Hollander, Jody L. Martin, Darrell D. Belke, Brian T. Scott, Eric Swanson, Vignesh Mouse Model Shock Protein 27 Mutant Protects Against Ischemia/Reperfusion Injury in a Transgenic Overexpression of Wild-Type Heat Shock Protein 27 and a Nonphosphorylatable Heat Print ISSN: 0009-7322. Online ISSN: 1524-4539 Copyright © 2004 American Heart Association, Inc. All rights reserved. is publishe...
full texto 27: traumatic brain injury and inflammation
traumatic brain injury (tbi) is a significant public health concern in our country, because of placing in top three most common causes of death and substantial direct and indirect costs to society. the incidence of tbi in our country is 1.7 times of international incidence. traumatic brain injury induced by primary and secondary mechanisms that give rise to death and neurologic morbidity in pat...
full textMy Resources
Journal title
volume 17 issue 2
pages 119- 122
publication date 2014-02-01
By following a journal you will be notified via email when a new issue of this journal is published.
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023