Title of article :
The Serum Changes of Neuron-Specific Enolase and Intercellular Adhesion
Molecule-1 in Patients With Diffuse Axonal Injury Following Progesterone
Administration: A Randomized Clinical Trial
Author/Authors :
Shahrokhi، Nader نويسنده , , Soltani، Zahra نويسنده Brain and Spinal Injury Research Center (BASIR), Tehran University of Medical Sciences, Tehran, IR Iran , , Khaksari، Mohammad نويسنده , , Karamouzian، Saeid نويسنده Department of Neurosurgery, Kerman University of Medical
Sciences, Kerman, IR Iran , , Mofid، Behshad نويسنده Department of Neurosurgery, Kerman University of Medical
Sciences, Kerman, IR Iran , , Asadikaram، Gholamreza نويسنده ,
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2016
Abstract :
Improvement of neurologic outcome in progesterone-administered
patients with diffuse axonal injury (DAI) has been found in a recent
study. Also, there has been interest in the importance of serum
parameters as predictors of outcome in traumatic brain injury. The aim
of this study was to examine the effect of progesterone administration
on serum levels of neuron-specific enolase (NSE), and intercellular
adhesion molecule-1 (ICAM-1) in clinical DAI. In this study, the serum
levels of ICAM-1 and NSE of 32 male DAI patients (18 - 60 years of age,
a Glasgow coma scale of 12 or less, and admitted within 4 hours after
injury) who were randomized for a controlled phase II trial of
progesterone were analyzed. The analysis was performed between the
control and progesterone groups at admission time, and 24 hours and six
days after DAI, respectively. A reduction in the serum level of ICAM-1
was noticed in the progesterone group 24 hours after the injury (P
< 0.05). There was no significant difference in the serum level
of NSE between the study groups during evaluation. At 24 hours after the
injury, the level of ICAM-1 in the control group was higher than that at
admission time (P < 0.05). The lowest level of NSE in the two
groups was seen six days after DAI (P < 0.01). In summary,
progesterone administration reduced serum ICAM-1, and whereby may
attenuate blood brain barrier disruption, the latter needs further
investigation for confirmation.
Journal title :
Archives of Trauma Research
Journal title :
Archives of Trauma Research