Effect of recombinant human growth hormone in the treatment of visceral fat accumulation in HIV infection

被引:77
作者
Engelson, ES
Glesby, MJ
Mendez, D
Albu, JB
Wang, J
Heymsfield, SB
Kotler, DP
机构
[1] Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Div Gastroenterol, New York, NY 10025 USA
[2] Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Div Endocrinol & Metab,Obes Res Ctr, New York, NY 10025 USA
[3] Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Body Composit Unit,Dept Med, New York, NY 10025 USA
[4] Commun Res Initiat AIDS, New York, NY USA
关键词
HIV; growth hormone; lipodystrophy; clinical trials; body composition; glucose tolerance; lipids; quality of life;
D O I
10.1097/01.QAI.0000020501.93209.1C
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HIV-associated lipodystrophy often includes excess accumulation of visceral fat. Recombinant human growth hormone (rhGH) is a potential treatment for the excess visceral fat. Prospective, open-label trials of 24 weeks of rhGH 6 mg/d and 24 weeks of 4 mg every other day were conducted with an intervening washout period of 12 weeks. Thirty HIV-positive participants (26 men and 4 women) with visceral adiposity were enrolled. The main outcome measure was change in visceral adipose tissue (VAT) on whole-body magnetic resonance imaging scan. Changes in whole-body subcutaneous adipose tissue and skeletal muscle, glucose metabolism, serum lipids, and quality of life were also assessed. Despite stable body weight, VAT decreased in evaluable subjects an average of 42% with rhGH 6 mg/d (n = 24; p < .001) and 15% with 4 mg every other day (n = 10; p < .01) after 12 weeks, with trends toward further decreases after an additional 12 weeks at each dose. Subcutaneous adipose tissue also decreased, but proportionately less and not significantly on the lower dose. Skeletal muscle increased. Body composition rebounded to or near baseline after the washout period. Effects on lipids were inconsistent. Total cholesterol levels fell on the higher dose only, whereas high-density lipoprotein cholesterol levels increased on the lower dose only, and there was no effect on triglyceride levels. Joint pain was the most common adverse event, and was reflected in subjective quality of life measurements as an increase in bodily pain. Insulin sensitivity fell, and 4 participants developed diabetes. Other adverse events included cancer of unknown relationship to treatment in 3 participants. Levels of distress decreased after 24 weeks on the higher dose. In conclusion, rhGH effectively reduces the excess visceral adipose tissue often associated with HIV fat redistribution/lipodystrophy. However, frequent adverse effects warrant controlled studies and careful patient monitoring, especially regarding glucose tolerance.
引用
收藏
页码:379 / 391
页数:13
相关论文
共 51 条
[1]  
[Anonymous], 1997, ANAL INCOMPLETE MULT, DOI DOI 10.1201/9781439821862
[2]  
[Anonymous], 2000, DIABETES CARE S1, V23, pS20
[3]   Evaluating changes in health status in HIV-infected patients:: Medical Outcomes Study-HIV and Multidimensional Quality of Life-HIV quality of life questionnaires [J].
Badia, X ;
Podzamczer, D ;
Casado, A ;
López-Lavid, C ;
García, M .
AIDS, 2000, 14 (10) :1439-1447
[4]  
BJORNTORP P, 1988, DIABETES METAB REV, V4, P615, DOI 10.1002/dmr.5610040607
[5]  
Bjorntorp P, 1996, INT J OBESITY, V20, P291
[6]   METABOLIC IMPLICATIONS OF BODY-FAT DISTRIBUTION [J].
BJORNTORP, P .
DIABETES CARE, 1991, 14 (12) :1132-1143
[7]   Effects of growth hormone treatment on visceral adipose tissue [J].
Brummer, RJM .
GROWTH HORMONE & IGF RESEARCH, 1998, 8 :19-23
[8]   A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors [J].
Carr, A ;
Samaras, K ;
Burton, S ;
Law, M ;
Freund, J ;
Chisholm, DJ ;
Cooper, DA .
AIDS, 1998, 12 (07) :F51-F58
[9]   Pathogenesis of the insulin resistance syndrome (Syndrome X) [J].
Chisholm, DJ ;
Campbell, LV ;
Kraegen, EW .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1997, 24 (9-10) :782-784
[10]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497