A placebo-controlled, dose-ranging study of a growth hormone releasing factor in HIV-infected patients with abdominal fat accumulation

被引:57
作者
Falutz, J
Allas, S
Kotler, D
Thompson, M
Koutkia, P
Albu, J
Trottier, B
Routy, JP
Cote, P
Abribat, T
Grinspoon, S
机构
[1] Massachusetts Gen Hosp, Program Nutr Metab, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Boston, MA USA
[3] Clin Med Actuel, Montreal, PQ, Canada
[4] Clin Med Quartier Latin, Montreal, PQ, Canada
[5] Royal Victoria Hosp, Div Hematol, Montreal, PQ, Canada
[6] Royal Victoria Hosp, Immunodeficiency Serv, Montreal, PQ, Canada
[7] Theratechnologies, St Laurent, PQ, Canada
[8] ARCA, Atlanta, GA USA
[9] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[10] St Lukes Roosevelt Hosp, Div Gastroenterol, New York, NY 10025 USA
[11] St Lukes Roosevelt Hosp, Div Endocrinol, New York, NY 10025 USA
[12] McGill Univ, Ctr Hlth, Montreal Gen Hosp, Immunodeficiency Treatment Ctr, Montreal, PQ, Canada
关键词
HIV; growth hormone releasing hormone; abdominal fat accumulation; lipodystrophy;
D O I
10.1097/01.aids.0000180099.35146.30
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To investigate the effects of TH9507, a novel growth hormone releasing factor, on abdominal fat accumulation, metabolic and safety parameters in HIV-infected patients with central fat accumulation. Design and methods: Randomized, double-blind, placebo-controlled trial enrolling 61 HIV-infected patients with increased waist circumference and waist-to-hip ratio. Participants were randomized to placebo or 1 or 2 mg TH9507 subcutaneously, once daily for 12 weeks. The primary outcome was change in abdominal fat, assessed by dual energy X-ray absorptiometry and cross-sectional computerized tomography scan. Secondary endpoints included change in insulin-like growth factor-l (IGF-l), metabolic, quality of life, and safety parameters. Results: TH9507 resulted in dose-related physiological increases in IGF-l (P < 0.01 for 1 mg (+48%) and 2 mg (+65%) versus placebo). Trunk fat decreased in the 2 mg group versus placebo (0.8, -4.6 and -9.2%; placebo, 1 and 2 mg, respectively, P = 0.014 for 2 mg versus placebo), without significant change in limb fat. Visceral fat (VAT) decreased most in the 2 mg group (-5.4, -3.6 and -15.7%; placebo, 1 and 2 mg, respectively) but this change was not significant versus placebo. Subcutaneous fat (SAT) was preserved and did not change between or within groups. Lean body mass and the ratio of VAT to SAT improved significantly in both treatment groups versus placebo. Triglyceride and the cholesterol to high-density lipoprotein ratio decreased significantly in the 2 mg group versus placebo. Treatment was generally well tolerated without changes in glucose. Conclusions: TH9507 reduced truncal fat, improved the lipid profile and did not increase glucose levels in HIV-infected patients with central fat accumulation. TH9507 may be a beneficial treatment strategy in this population, but longer-term studies with more patients are needed to determine effects on VAT, treatment durability, and safety. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1279 / 1287
页数:9
相关论文
共 31 条
[1]  
ABRIBAT T, 2001, END SOC 84 ANN M 200
[2]  
ALEXANDRE B, 2003, EFFECTS GENDER IGF 1, P2
[3]   Impact of lipodystrophy on the quality of life of HIV-1-infected patients [J].
Blanch, J ;
Rousaud, A ;
Martínez, E ;
De Lazzari, E ;
Peri, JM ;
Milinkovic, A ;
Perez-Cuevas, TB ;
Blanco, TL ;
Gatell, JM .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2002, 31 (04) :404-407
[4]   Reduced bone mineral density in human immunodeficiency virus-infected patients and its association with increased central adiposity and postload hyperglycemia [J].
Brown, TT ;
Ruppe, MD ;
Kassner, R ;
Kumar, P ;
Kehoe, T ;
Dobs, AS ;
Timpone, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (03) :1200-1206
[5]   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
[6]  
CLEMMONS D, 2003, SAFETY ASSESSMENT ME
[7]   Improved cardiovascular risk factors and cardiac performance after 12 months of growth hormone (GH) replacement in young adult patients with GH deficiency [J].
Colao, A ;
Di Somma, C ;
Cuocolo, A ;
Spinelli, L ;
Tedesco, N ;
Pivonello, R ;
Bonaduce, D ;
Salvatore, M ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (05) :1874-1881
[8]   Effect of recombinant human growth hormone in the treatment of visceral fat accumulation in HIV infection [J].
Engelson, ES ;
Glesby, MJ ;
Mendez, D ;
Albu, JB ;
Wang, J ;
Heymsfield, SB ;
Kotler, DP .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2002, 30 (04) :379-391
[9]   Combination antiretroviral therapy and the risk of myocardial infarction [J].
Friis-Moller, N ;
Sabin, CA ;
Weber, R ;
Monforte, AD ;
El-Sadr, WM ;
Reiss, P ;
Thiébaut, R ;
Morfeldt, L ;
De Wit, S ;
Pradier, C ;
Calvo, G ;
Law, MG ;
Kirk, O ;
Phillips, AN ;
Lundgren, JD ;
Lundgren, JD ;
Weber, R ;
Monteforte, AD ;
Bartsch, G ;
Reiss, P ;
Dabis, F ;
Morfeldt, L ;
De Wit, S ;
Pradier, C ;
Calvo, G ;
Law, MG ;
Kirk, O ;
Phillips, AN ;
Houyez, F ;
Loeliger, E ;
Tressler, R ;
Weller, I ;
Friis-Moller, N ;
Sabin, CA ;
Sjol, A ;
Lundgren, JD ;
Sawitz, A ;
Rickenbach, M ;
Pezzotti, P ;
Krum, E ;
Meester, R ;
Lavignolle, V ;
Sundström, A ;
Poll, B ;
Fontas, E ;
Torres, F ;
Petoumenos, K ;
Kjær, J ;
Hammer, S ;
Neaton, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (21) :1993-2003
[10]  
GRUNFELD C, 2002, 14 INT AIDS C BARC S, P81