Document 1033 DOCN M94A1033 TI Effects of enteral nutrition supplements on HIV disease. DT 9412 AU Cope FO; Hellerstein M; University of California, San Francisco. SO Int Conf AIDS. 1994 Aug 7-12;10(2):224 (abstract no. PB0910). Unique Identifier : AIDSLINE ICA10/94371542 AB A doubleblind, prospective, randomized trial evaluated the effects of enteral nutrition supplementation on nutrient intake, body composition, GI symptoms, nutritional status and AIDS specific surrogate markers in subjects with AIDS or HIV-associated weight loss (13.2 +/- 4.2% body wt). A whole protein (WP) and a peptide-based (PB) formula were administered over 1 yr with evaluations at 6 weeks, 6 months and 12 months. Subjects ingested up to two 8 oz cans/day. Both formulas were well-tolerated and there were no adverse effects on GI function or related symptoms. Evaluation of food and formula intake at 6 months revealed an increased intake of calories and protein in both groups. This occurred through supplement intake (500-600 kcal/day and 17-28g protein/day) which resulted in some decrease in spontaneous food intake (196-382 kcal/day and 5.6-14.45 protein/day). The net increase was approximately 400 kcal/day. REE was elevated compared to normals (110% predicted) at baseline & did not change during supplementation. The response of fat free mass (FFM) at 6 wks was significantly correlated (r2 = -0.42, p < 0.01) with baseline hepatic fat synthesis (an index of cytokine presence and metabolic dysregulation). A majority of patients maintained their entrance body weight as only 20% experienced reductions of 2.2 kg or greater. When considering all data from the 1 yr followup, the risk of a > or = 50% drop from baseline in the CD4 count was 7.4 times greater in the WP than the PB group (p < 0.01). In conclusion, total intake of nutrients increased even after reduction of voluntary food intake was considered. This increased macro and micro nutrient intake resulted in apparent weight maintenance without untoward GI symptom or function. Specific dietary management with the PB formula may provide added clinical benefit based on the CD4 analyses. DE Acquired Immunodeficiency Syndrome/COMPLICATIONS/*THERAPY Cachexia/ETIOLOGY/*THERAPY Caloric Intake/DRUG EFFECTS Double-Blind Method *Enteral Nutrition Human Nutritional Status/DRUG EFFECTS Prospective Studies CLINICAL TRIAL MEETING ABSTRACT RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).