Background & Aims: Rheumatoid arthritis (RA) is complicated by cytokine-driven alterations in protein and energy metabolism and consequent muscle wasting (cachexia). The aim of this randomised controlled trial was to investigate the efficacy of a mixture of β-hydroxy-β-methylbutyrate, glutamine and arginine (HMB/GLN/ARG) as nutritional treatment for rheumatoid cachexia. Methods: Forty RA patients supplemented their diet with either HMB/GLN/ARG or a nitrogen (7.19 g/day) and calorie (180 kcal/day) balanced mixture of alanine, glutamic acid, glycine, and serine (placebo) for 12 weeks. Body composition and other outcomes were assessed at baseline and follow-up, and analysed by mixed ANOVA. Results: Dietary supplementation with HMB/GLN/ARG was not superior to placebo in the treatment of rheumatoid cachexia (group × time interactions P > 0.05 for all outcomes). Both amino acid mixtures significantly increased (main effect of time) fat-free mass (727±1186 g, P < 0.01), total body protein (719±1703 g, P = 0.02), arms (112±183 g, P < 0.01) and legs (283±534 g, P < 0.01) lean mass, and some measures of physical function. No significant adverse event occurred during the study, but patients in the HMB/GLN/ARG group reported fewer gastrointestinal complaints compared to placebo. Conclusions: Dietary supplementation with HMB/GLN/ARG is better tolerated but not more effective in reversing cachexia in RA patients compared to the mixture of other non-essential amino acids used as placebo. Further controlled studies are necessary to confirm the beneficial anabolic and functional effects of increased nitrogen intake in this population. © 2005 Elsevier Ltd. All rights reserved.

Marcora, S., Lemmey, A., Maddison, P. (2005). Dietary treatment of rheumatoid cachexia with β-hydroxy-β-methylbutyrate, glutamine and arginine: A randomised controlled trial. CLINICAL NUTRITION, 24(3), 442-454 [10.1016/j.clnu.2005.01.006].

Dietary treatment of rheumatoid cachexia with β-hydroxy-β-methylbutyrate, glutamine and arginine: A randomised controlled trial

Marcora, S.;
2005

Abstract

Background & Aims: Rheumatoid arthritis (RA) is complicated by cytokine-driven alterations in protein and energy metabolism and consequent muscle wasting (cachexia). The aim of this randomised controlled trial was to investigate the efficacy of a mixture of β-hydroxy-β-methylbutyrate, glutamine and arginine (HMB/GLN/ARG) as nutritional treatment for rheumatoid cachexia. Methods: Forty RA patients supplemented their diet with either HMB/GLN/ARG or a nitrogen (7.19 g/day) and calorie (180 kcal/day) balanced mixture of alanine, glutamic acid, glycine, and serine (placebo) for 12 weeks. Body composition and other outcomes were assessed at baseline and follow-up, and analysed by mixed ANOVA. Results: Dietary supplementation with HMB/GLN/ARG was not superior to placebo in the treatment of rheumatoid cachexia (group × time interactions P > 0.05 for all outcomes). Both amino acid mixtures significantly increased (main effect of time) fat-free mass (727±1186 g, P < 0.01), total body protein (719±1703 g, P = 0.02), arms (112±183 g, P < 0.01) and legs (283±534 g, P < 0.01) lean mass, and some measures of physical function. No significant adverse event occurred during the study, but patients in the HMB/GLN/ARG group reported fewer gastrointestinal complaints compared to placebo. Conclusions: Dietary supplementation with HMB/GLN/ARG is better tolerated but not more effective in reversing cachexia in RA patients compared to the mixture of other non-essential amino acids used as placebo. Further controlled studies are necessary to confirm the beneficial anabolic and functional effects of increased nitrogen intake in this population. © 2005 Elsevier Ltd. All rights reserved.
2005
Marcora, S., Lemmey, A., Maddison, P. (2005). Dietary treatment of rheumatoid cachexia with β-hydroxy-β-methylbutyrate, glutamine and arginine: A randomised controlled trial. CLINICAL NUTRITION, 24(3), 442-454 [10.1016/j.clnu.2005.01.006].
Marcora, S.; Lemmey, A.; Maddison, P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/745996
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