Several studies have shown beneficial effects of recombinant human growth hormone (r-hGH) in reducing visceral adipose tissue (VAT) in HIV-1-infected patients with lipodystrophy.
MethodsPatients were randomized to r-hGH 4 mg daily (group A) or three times per week (group B) over 12 weeks, followed by a 2 mg daily maintenance dose for 12 weeks. Magnetic resonance imaging (MRI) scans were performed to assess body composition.
ResultsA total of 26 subjects were included in the study. VAT was reduced overall by 35.1 cm 2 (29.5%) at week 12 and by 49 cm 2 (39.9%) at week 24, respectively, compared with baseline (Po0.001 for both comparisons). By week 12, VAT was reduced by 27 and 29% (A vs B; P 5 0.47) while facial fat was reduced by 3.3 and 2.6 cm 2 in groups A and B, respectively (P 5 0.96). Over 24 weeks, VAT was reduced by 42 and 38% (P 5 0.35) and facial fat by 3.2 and 2.4 cm 2 in groups A and B, respectively (P 5 0.91), compared with baseline. There was a greater increase in high-density lipoprotein (HDL) in group A than in group B (4.9 vs 2.4 mg/dL in week 12 and 7.1 vs À 0.4 mg/dL in week 24; P 5 0.03). Fasting insulin levels increased, whereas glucose and insulin measured in oral glucose tolerance tests remained unchanged. Drug-related side effects were transient and reversible, but more common in group A (67%) than in group B (29%).
ConclusionsThis study confirms reports that r-hGH effectively reduces VAT, with a relatively small reduction of facial and limb fat.Keywords: growth hormone, lipodystrophy, magnetic resonance imaging, visceral adipose tissue, visceral adiposity
IntroductionIn recent years, HIV-associated lipodystrophy syndrome has become a major challenge in the treatment of HIV disease. This syndrome involves intra-abdominal (visceral) adiposity, development of antero-and dorsocervical fat pads (buffalo hump), breast enlargement and symmetric lipomatosis as signs of fat accumulation, and loss of subcutaneous fat from the face, limbs, trunk and buttocks [1][2][3][4][5]. All of these changes can occur alone or in combination. To date, the exact pathogenesis of the broad spectrum of these common, disfiguring body shape changes, which can occur at any stage of treated HIV 397 infection, is not completely understood. Visceral adiposity, one of the hallmarks of HIV-associated lipodystrophy syndrome, is a known independent risk factor for insulin resistance and cardiovascular complications [6][7][8] and is therefore a major concern as a potential long-term complication of highly active antiretroviral therapy (HAART). Recent studies suggest an increase of cardiovascular and cerebrovascular events associated with the duration of HAART, although some results are contradictory [9][10][11][12][13][14][15][16]. Several studies using various antiretroviral treatment strategies failed to completely resolve or prevent HIV-associated lipodystrophy. Furthermore, expensive and time-consuming three-dimensional imaging techniques such as computed tomography or magnetic resonance imaging (MRI) are needed to disting...