Update on clinical trials of growth factors and anabolic steroids in cachexia and wasting1234

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This article and others that focused on the clinical features, mechanisms, and epidemiology of skeletal muscle loss and wasting in chronic diseases, which include chronic kidney disease, cancer, and AIDS, were presented at a symposium entitled “Cachexia and Wasting: Recent Breakthroughs in Understanding and Opportunities for Intervention,“ held at Experimental Biology 2009. The clinical and anabolic efficacy of specific growth factors and anabolic steroids (eg, growth hormone, testosterone, megestrol acetate) in malnutrition and other catabolic states has been the subject of considerable research during the past several decades. Research on the effects of these agents in cachexia or wasting conditions, characterized by progressive loss of skeletal muscle and adipose tissue, focused on patients with AIDS in the early 1990s, when the devastating effects of the loss of body weight, lean body mass, and adipose tissue were recognized as contributors to these patients’ mortality. These same agents have also been studied as methods to attenuate the catabolic responses observed in cancer-induced cachexia and in wasting induced by chronic obstructive pulmonary disease, congestive heart failure, renal failure, and other conditions. This article provides an updated review of recent clinical trials that specifically examined the potential therapeutic roles of growth hormone, testosterone, oxandrolone, and megestrol acetate and emerging data on the orexigenic peptide ghrelin, in human cachexia and wasting.

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1

From the Department of Radiation Oncology (NPG), the Department of Medicine (GH and TRZ), the Center for ClinicalMolecular Nutrition (NPG, GH, and TRZ), and Emory University Hospital Nutrition and Metabolic Support Service (GH and TRZ), Emory University School of Medicine Atlanta GA.

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Presented at the symposium “Cachexia and Wasting: Recent Breakthroughs in Understanding and Opportunities for Intervention,” held at Experimental Biology 2009, New Orleans, LA, 18 April, 2009.

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Supported by National Institutes of Health grants K24 RR023356 and UL1 RR025008 (TRZ).

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Address correspondence to TR Ziegler, Atlanta Clinical and Translational Science Institute, Room GG-23, Emory University Hospital, 1364 Clifton Road, Atlanta GA, 30322. E-mail: [email protected].