Bridging the Gap: Conference Record [Abstract book, International Conference on AIDS (12th: 1998: Geneva, Switzerland)]

12th World AIDS Conference Abstracts 42254-42339 841 42335 The effects of oxandrolone (OX) plus resistance exercise (RE) on Unitrogen Balance (N BAL), body composition and strength in men with AIDS wasting syndrome (AWS) Alison Strawford, T. Barbieri2, M. Van Loan2, E.J. Parks3, J. King2, N. Barton4, M.K. Hellerstein2. Nutritional Sciences, Morgan Hall, UC Berkeley, Berkeley, CA 94720; 2 Western Human Nutrition Research Center, San Francisco, CA; 3Nutritional Sciences, UC Berkeley Berkeley, CA; 4 Biotechnology General Corp., New Jersey NJ, USA Background: LBM loss is related to time of death in HIV/AIDS and restoration of LBM may improve survival. Methods: We compared OX (20 mg/day) plus RE to placebo (P) plus RE in men with AWS (n = 23, 92 ~ 3% usual weight, age 41 + 8 yrs, serum total testosterone (T) 556 ~ 298 ng/dL mean ~ S.D) in an 8 wk placebo-controlled randomized study. To assure uniform T levels during the study, all subjects received T at replacement doses (100 mg IM/wk). 13/23 subjects were receiving protease inhibitors (weight stable >3 months). 10-day in-patient N Bal studies were performed at baseline and after 4 weeks of treatment. Controlled RE was carried out 3 times/wk under supervision. Follow up measurements of body composition by DEXA, strength by 1-repetition max (1 RM) and dynamometer were carried out at 8 wks. Results: (1) N retention increased significantly from baseline in both groups (+3.8 ~ 1.8 g/day P/RE, +5.6 ~ 2.1 g/day OX/RE, p < 0.05 between groups) representing a gain of 0.9 ~ 0.4 Kg LBM/wk for P/RE and 1.3 ~ 0.5 Kg/wk for OX/RE. (2) Weight and LBM increased significantly from baseline in both groups (weight 4.2 ~ 2.8 Kg, LBM 3.8 + 2.9 Kg (P/RE group); weight 6.7 ~ 2.0 Kg, LBM 6.9 1 1.7 Kg (OX/RE group); p < 0.05 vs baseline and between groups (see figure). (3) Strength improved in both groups (1 RM chest press 18 ~ 8% vs 34 ~ 6%, leg press 28: 4% vs 38 ~ 8%, in P/RE and OX/RE groups respectively, data mean ~ S.E.). Strength by dynamometry also improved and was significantly greater in OX/RE than P/RE (see figure). (4) Viral load (baseline 45,900 ~ 27,500, mean ~ S.E.) did not change significantly. (5) LBM gain continued over the 12 weeks of open-label therapy (1.0 4 2.5 Kg LBM for whole group).: IjP/RI 0 OX/iRl 42337 Zinc deficiency profoundly increases risk for HIV-1 related mortality Marianna Baum, G. Shor-Posner, S. Lai, H. Lai, E. Perez, J.B. Page. University of Miami, Room 1006, 1400 NW 10th Ave, Miami, FL, USA Objective: Zinc is thought to promote activity of the HIV-1 virus. This trace element is, however, essential for maintaining a healthy immune system. As zinc deficiency is prevalent in HIV/AIDS, the aim of this study was to evaluate zinc status, disease progression and HIV-1 related mortality Design: A longitudinal study was conducted over 3.5 years in 118 HIV-1 seropositive men and women who abuse drugs. Methods: Zinc intake was examined in relation to plasma zinc levels, CD4 cell count and HIV-related mortality. A multivariate Cox model, adjusted for age, sex, race and CD4 cell count over time was used to analyze the longitudinal data. Results: Eighty-six percent of the HIV-1 infected drug users consumed dietary intake below the recommended dietary allowance and 56% of the group had plasma zinc levels considered deficient (<0.75 t<g/ml). Plasma zinc levels were positively associated (p = 0.005) with CD4 cell count, and overtly low plasma zinc was associated (p = 0.002) with advanced disease (CD4 <200 cells/mm3). While plasma zinc has been previously described as a marker of disease progression, those with higher intake of zinc over time, exhibited significantly higher levels of plasma zinc (p < 0.0001). In addition, low dietary zinc intake (below the median of 9.34 mg/day) was significantly associated with a dramatic risk for mortality (RH = 36.97, p < 0.03). Conclusions: The significant association between dietary and plasma zinc, and poor survival in HIV-1 infection indicates that adequate amounts of dietary zinc are needed to slow disease progression. Zinc therapy in HIV+ individuals who have overtly low plasma zinc levels needs to be investigated. 42338 Nutritional status and health-related quality of life in patients infected with HIV Lawrence Kim, M. Keiserman, J. Maimares Schmidt, J. Tuveson, J. Koch. Univ. Calif San Francisco, 1001 Potrero Avenue 3D, San Francisco, CA 94110, USA Background: Weight loss is an independent predictor of mortality among patients infected with HIV. However, whether overall weight loss or specific loss of fat mass or body cell mass impact individual dimensions of health-related quality of life (QOL) has not been studied. Methods: All patients referred for evaluation to the Gastroenterology-HIV-Nutrition clinic were asked to complete the Rand SF-36 Health Survey questionnaire (a standardized QOL measurement). Body weight and height were measured. Bioelectrical impedance analysis (BIA) was performed to determine fat mass (%FAT) and body cell mass (%BCM) as a percentage of total body mass. Results: 69 patients completed questionnaires and BIA measurements (65 male, mean age 39, median CD4 cell count 166/mm3). In univariate analyses, %BCM was associated with QOL subscales pertaining to physical functioning and general health. In contrast, no significant associations were found between weight as percentage of usual body weight (%UBW) or %FAT and any subscales. No association was seen for %BCM and QOL subscales pertaining to emotional well-being, energy, and social functioning. I M~, =E. * t 21, oS -111 Conclusions: Both OX/RE and P/RE resulted in a robust anabolic effect, without adverse side effects or increases in VL. OX/RE showed a significantly greater improvement in nitrogen retention, LBM accrual and strength than the P/RE group. Studies of other treatment combinations and earlier intervention prior to the onset of AWS will be of interest. 42336 Glutamine/antioxidant supplementation promotes gain in body cell mass in HIV patients with weight loss Judith Shabert1, Charmaine Winslow2, J.K. Shabert', J. Lacey3, D.W. Wilmore1. 1Brigham And Women's Hospital 75 Francis Street, Boston, MA; 2Nutrition Specialty Center, Bocaraton, FL; 3Simmons College, Boston, Ma, USA Loss of body cell mass (BCM), the active functioning tissue of the body, commonly occurs in patients with HIV infection; the extent of wasting is related to the length of survival. In order to evaluate the role of the amino acid L-glutamine (GLN) and antioxidants on AIDS-associated wasting, we studied 26 individuals with weight loss _-10% of ideal. Subjects were randomized to receive GLN/antioxidants 40 g/d (Cambridge Nutraceuticals, Boston, MA) in divided doses or glycine (40 g/d) as placebo for 12 weeks. Throughout the study, the subjects were seen weekly by a nutritionist and bioelectrical impedance analysis, [(BIA), RJL Systems, Clinton MI)], body weight and nutrition counseling were performed. Twenty one subjects (average age 39 yr, 19 M, 2 F) completed the study. Five patients were excluded for the following: death (1 control), major change in antiretroviral drugs (1 control), terminated for personal reasons (2 control, 1 GLN). The values for the two groups are shown below (mean ~ SD) SF36 Subscale Physical Functioning Role Limits due to Physical Health General Health % UBW Coeff p 13.5 0.60 21.0 0.53 24.7 0.20 % FAT Coeff p 0.27 0.53 0.15 0.80 0.14 0.65 % BCM Coeff p 0.90 0.003 0.79 0.05 0.47 0.03 Control pre post Weight (kg) 71.6 + 11.2 71.9+ 11.2 Body cell mass (kg) 28.4 i 6.0 28.8 1 6.1 Total body water (1) 43.3 ~ 8.0 43.5 ~ 7.8 Intracellular water (1) 25.9 i 5.4 26.5 1 5.4 Extracellular water (1) 17.3 4 2.9 17.0 + 2.8 P. 0.002 and P - 0.02 GLN/Antioxidant pre post 68.3 + 8.3 70.6 1 8.9 26.9 4 4.5 28.6 ~ 4.6 42.3 ~ 5.0 43.8 + 5.7* 25.6 ~ 4.7 27.3 ~ 5.0" 16.7 1.3 16.4 ~ 1.8 All significant univariate associations between %BCM and QOL subscales remained significant after adjustment for age, sex, and CD4 count. The association between %BCM and QOL subscales was also independent of %FAT in multivariate analysis (p < 0.10). Conclusion: Physical aspects of health-related quality of life among patients with HIV are strongly associated with percentage body cell mass. In contrast, body weight and estimates of fat percentage do not predict quality of life. Body composition analysis is a better indicator of functional status in patients with HIV than body weight. Interventions that improve body cell mass should be assessed for corresponding improvements in physical function and quality of life. 142339 Protein intake is associated with body cell mass in weight-stable HIV+ men with CD4 < 200 cells/mm3: CPCRA 038 S. Bruce Williams', G. Collins2, N. Muurahainen3, G. Bartsch2, C. Gibert4, S.S. Raghavan5, D. Wheeler6. Comm. Prog. for Clin. Research on AIDS, 12211 Lomas Blvd. NE; Albuquerque, NM; 2Minneapolis, MN; 3Philadelphia, PA, 4 Washington, DC; 5New York, NY; 6Annandale, VA, USA Objective: To determine the associations of body cell mass (BCM), total body fat (TBF), and extracellular mass (ECM) with macronutrient intake among HIV+ men in the United States with CD4 count <200 cells/mm3 and documented stable weight. Methods: Measurements of BCM, TBF, and ECM by bioelectrical impedance analysis and macronutrient intake by 24 hour food recall were made at baseline GLN/antioxidant nutrient supplement can increase body weight, body cell mass and intracellular water when compared to placebo controls. The specific tissues which account for the increase in BCM by GLN/antioxidant supplementation have yet to be defined but this approach provides a highly cost-effective therapy for the rehabilitation of HIV patients with weight loss.

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Title
Bridging the Gap: Conference Record [Abstract book, International Conference on AIDS (12th: 1998: Geneva, Switzerland)]
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International AIDS Society
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Page 841
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1998
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"Bridging the Gap: Conference Record [Abstract book, International Conference on AIDS (12th: 1998: Geneva, Switzerland)]." In the digital collection Jon Cohen AIDS Research Collection. https://name.umdl.umich.edu/5571095.0140.073. University of Michigan Library Digital Collections. Accessed May 10, 2025.
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