Growth hormone effects on hypertrophic scar formation: a randomized controlled trial of 62 burned children

被引:16
作者
De Oliveira, GV
Sanford, AP
Murphy, KD
De Oliveira, HM
Wilkins, JP
Wu, XW
Hawkins, HK
Kitten, G
Chinkes, DL
Barrow, RE
Herndon, DN
机构
[1] Shriners Hosp Children, Galveston, TX 77550 USA
[2] Univ Texas, Med Branch, Dept Surg, Galveston, TX 77550 USA
[3] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77550 USA
[4] Univ Texas, Med Branch, Dept Dermatol, Galveston, TX 77550 USA
[5] Univ Fed Minas Gerais, Dept Morphol, Belo Horizonte, MG, Brazil
关键词
D O I
10.1111/j.1067-1927.2004.012407.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The hypercatabolism after massive pediatric burns has been effectively treated with recombinant human growth hormone, an anabolic agent that stimulates protein synthesis and abrogates growth arrest. While experimental studies have shown increased potential for fibrosis induced by growth hormone therapy, adverse effects on human scars have not been investigated. Our aim was to evaluate hypertrophic scar formation in 62 patients randomized to receive injections of 0.05 mg/kg/day of recombinant human growth hormone or placebo, from discharge until 1 year after burn. Scar scales were used to evaluate scar-severity at discharge, 6, 9, 12, and 18-24 months after burn, by three observers blinded to treatment. Computer-assisted planimetry allowed quantification of percentage of hypertrophic scar formation. Types I and III collagens were localized and quantified in scars and normal skin of patients from both groups, using immunohistochemistry with confocal laser microscopy analysis. Insulin-like growth factor-1 blood levels helped assess compliance. Statistical analysis showed that scar hypertrophy significantly increased from 6 to 12 months after injury in both groups, while decreasing at 18-24 months postburn. Types I and III collagens were statistically increased in the reticular layer of scars from both groups when compared to paired normal skin. Insulin-like growth factor-1 was significantly increased in the recombinant human growth factor-treated group. No differences were seen when recombinant human growth factor and control groups were compared using the scar scales, planimetry, or immunohistochemistry. We concluded that recombinant human growth hormone therapy did not adversely affect scar formation and should not contraindicate the administration of recombinant human growth hormone as a therapeutic approach to severely burned children.
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收藏
页码:404 / 411
页数:8
相关论文
共 33 条
[11]   ROLE OF GROWTH-HORMONE IN THE DEVELOPMENT OF EXPERIMENTAL RENAL SCARRING [J].
ELNAHAS, AM ;
BASSETT, AH ;
COPE, GH ;
LECARPENTIER, JE .
KIDNEY INTERNATIONAL, 1991, 40 (01) :29-34
[12]  
Hansbrough John F., 1995, Journal of Burn Care and Rehabilitation, V16, P335, DOI 10.1097/00004630-199505000-00023
[13]   CONFOCAL LASER-SCANNING MICROSCOPY (CLSM) FOR THE STUDY OF COLLAGEN SPONGE MICROSTRUCTURE [J].
HANTHAMRONGWIT, M ;
GRANT, MH ;
WILKINSON, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1994, 28 (02) :213-216
[14]   The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease [J].
Hattersley, AT ;
Tooke, JE .
LANCET, 1999, 353 (9166) :1789-1792
[15]   CHANGES IN TYPE OF COLLAGEN DURING THE DEVELOPMENT OF HUMAN POST-BURN HYPERTROPHIC SCARS [J].
HAYAKAWA, T ;
HASHIMOTO, Y ;
MYOKEI, Y ;
AOYAMA, H ;
IZAWA, Y .
CLINICA CHIMICA ACTA, 1979, 93 (01) :119-125
[16]   EFFECTS OF RECOMBINANT HUMAN GROWTH-HORMONE ON DONOR-SITE HEALING IN SEVERELY BURNED CHILDREN [J].
HERNDON, DN ;
BARROW, RE ;
KUNKEL, KR ;
BROEMELING, L ;
RUTAN, RL .
ANNALS OF SURGERY, 1990, 212 (04) :424-431
[17]   CHARACTERIZATION OF GROWTH-HORMONE ENHANCED DONOR SITE HEALING IN PATIENTS WITH LARGE CUTANEOUS BURNS [J].
HERNDON, DN ;
HAWKINS, HK ;
NGUYEN, TT ;
PIERRE, E ;
COX, R ;
BARROW, RE .
ANNALS OF SURGERY, 1995, 221 (06) :649-659
[18]  
IRELAND G, 2003, ADVANTAGES CONFOCAL
[19]  
KNOX J, 1995, J TRAUMA, V39, P526
[20]  
Laguens RP, 1998, JPN HEART J, V39, P809