Effect of recombinant human growth hormone and insulin-like growth factor-1 administration on IGF-1 and IGF-binding protein-3 levels in brain injury

被引:8
|
作者
Rockich, KT
Hatton, JC
Kryscio, RJ
Young, BA
Blouin, RA
机构
[1] Univ Kentucky, Coll Pharm, Div Pharmaceut Sci, Lexington, KY 40536 USA
[2] Univ Kentucky, Coll Pharm, Div Pharm Practice & Sci, Lexington, KY 40536 USA
[3] Univ Kentucky, Coll Pharm, Div Stat, Lexington, KY 40536 USA
[4] Univ Kentucky, Coll Pharm, Div Neurosurg, Lexington, KY 40536 USA
[5] Univ Kentucky, Albert B Chandler Med Ctr, Lexington, KY 40536 USA
来源
PHARMACOTHERAPY | 1999年 / 19卷 / 12期
关键词
D O I
10.1592/phco.19.18.1432.30891
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study Objective. To assess the effect of recombinant human growth hormone (rhGH) on the insulin-like growth factor-1 (IGF-1) plasma concentration versus time profile during continuous infusion of recombinant human (rh)IGF-1 to patients with traumatic brain injury (TBI). Setting, University of Kentucky Chandler Medical Center. Patients. Twenty-three patients with TBI (aged 18-59 yrs) with Glascow Coma Scale scores of 4-10. Intervention. Patients were randomized to receive rhIGF-1 0.01 mg/kg/hour and daily subcutaneous doses of rhGH 0.05 mg/kg/day or saline for 14 days. Measurements and Main Results. Plasma concentrations of IGF-1 and IGF-binding protein (BP)-3 were quantified by radioimmunoassay. Patients receiving rhIGF-1/rhGH reached a peak IGF-1 concentration (1199.3 +/- 84.0 mu g/L) at 72 hours and maintained it throughout the study. Levels of IGF-1 in the control group did not change significantly above baseline throughout the study. Concentrations of IGFBP-3 were significantly higher after 48 hours in the treated group (5.1 +/- 0.4 mg/L) than in controls (2.9 +/- 0.5 mg/L) and continued until the end of the study (p<0.05). Conclusion. Infusion of rhIGF-1 in conjunction with rhGH effectively achieved, and maintained supraphysiologic IGF-1 plasma concentrations throughout the dosing period in patients with TBI. It. appears that rhGH alters the IGF-1 plasma concentration versus time profile during continuous administration. Although speculative, changes in protein binding of IGF-1 are the most likely mechanism.
引用
收藏
页码:1432 / 1436
页数:5
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