Hyperglycemia exacerbates muscle protein catabolism in burn-injured patients

Objective The purpose of this study was to assess if hyperglycemia influences energy expenditure or the extent of muscle protein catabolism in severely burned adults. Design Retrospective study. Setting Burn intensive care unit at a university hospital. Patients Adults with burns on ≥40% of their body surface area. Interventions Simultaneous measurement of indirect calorimetry and leg net balance of phenylalanine (as an index of muscle protein catabolism). Patients were stratified by plasma glucose values at the time of metabolic measurements (i.e., normal, glucose at ≤130 mg/dL; mild hyperglycemia, glucose at 130–200 mg/dL; severe hyperglycemia, glucose at >200 mg/dL). Measurements and Main Results Normal (n = 9; plasma glucose, 109 ± 13 mg/dL [mean ± sd]), mildly hyperglycemic (n = 13l plasma glucose, 156 ± 17 mg/dL), and severely hyperglycemic subjects (n = 7, glucose 231 ± 32 mg/dL) were similar in age, body weight, extent of burn area, and daily caloric intake. Severe hyperglycemia was associated with significantly higher arterial concentrations of phenylalanine (normal, 0.079 ± 0.027 &mgr;mol/L; severe hyperglycemia, 0.116 ± 0.028;p < .05) and a significantly greater net efflux of phenylalanine from the leg (normal, −0.067 ± 0.072 &mgr;mol·min−1·100 mL−1 leg volume; severe hyperglycemia, −0.151 ± 0.080 &mgr;mol·min−1·100 mL−1 leg volume;p < .05). Resting energy expenditure and respiratory quotient were similar between patient groups. Conclusions These findings demonstrate an association between hyperglycemia and an increased rate of muscle protein catabolism in severely burned patients. This suggests a possible link between resistance of muscle to the action of insulin for both glucose clearance and muscle protein catabolism.

[1]  D. F. Rochester,et al.  Respiratory muscle strength and maximal voluntary ventilation in undernourished patients. , 2015, The American review of respiratory disease.

[2]  D. Chinkes,et al.  Association of hyperglycemia with increased mortality after severe burn injury. , 2001, The Journal of trauma.

[3]  D. Herndon,et al.  The Effects of Hyperglycemia on Skin Graft Survival in the Burn Patient , 2000, Annals of plastic surgery.

[4]  D. Chinkes,et al.  Determinants of Skeletal Muscle Catabolism After Severe Burn , 2000, Annals of surgery.

[5]  R. Wolfe,et al.  Testosterone injection stimulates net protein synthesis but not tissue amino acid transport. , 1998, The American journal of physiology.

[6]  D. Barritault,et al.  Platelet releasate treatment improves skin healing in diabetic rats through endogenous growth factor secretion. , 1998, Cellular and molecular biology.

[7]  S. Lowry,et al.  Nutritional modulation of immunity and the inflammatory response. , 1998, Nutrition.

[8]  A. Barbul,et al.  Lymphocyte function in wound healing and following injury , 1998, The British journal of surgery.

[9]  V. Praloran,et al.  Thrombocytopenia in the sepsis syndrome: role of hemophagocytosis and macrophage colony-stimulating factor. , 1997, The American journal of medicine.

[10]  T. Hendriks,et al.  Complete prevention of impaired anastomotic healing in diabetic rats requires preoperative blood glucose control , 1996, The British journal of surgery.

[11]  M. Schwartz,et al.  Diabetes Complications--Why Is Glucose Potentially Toxic? , 1996, Science.

[12]  D. Rogers,et al.  The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus , 1994 .

[13]  R. Tattersall,et al.  The effects of 3-hydroxybutyrate and glucose on human T cell responses to Candida albicans. , 1993, FEMS immunology and medical microbiology.

[14]  J O Hill,et al.  Acute hyperglycemia enhances proteolysis in normal man. , 1993, The American journal of physiology.

[15]  S. Genuth,et al.  The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. , 1993, The New England journal of medicine.

[16]  D. Matthews Radioactive and Stable Isotope Tracers in Biomedicine: Principles and Practice of Kinetic Analysis , 1993 .

[17]  S. McClave,et al.  Differentiating subtypes (hypoalbuminemic vs marasmic) of protein-calorie malnutrition: incidence and clinical significance in a university hospital setting. , 1992, JPEN. Journal of parenteral and enteral nutrition.

[18]  G. Biolo,et al.  Harry M. Vars Research Award. A new model to determine in vivo the relationship between amino acid transmembrane transport and protein kinetics in muscle. , 1992, JPEN. Journal of parenteral and enteral nutrition.

[19]  R. Wolfe,et al.  Differentiation between septic and postburn insulin resistance. , 1989, Metabolism: clinical and experimental.

[20]  R. Wolfe,et al.  Role of insulin and glucose oxidation in mediating the protein catabolism of burns and sepsis. , 1989, The American journal of physiology.

[21]  R. Andrassy,et al.  Short-term hyperglycemia depresses immunity through nonenzymatic glycosylation of circulating immunoglobulin. , 1989, The Journal of trauma.

[22]  R. Wolfe,et al.  Dynamics of the protein metabolic response to burn injury. , 1988, Metabolism: clinical and experimental.

[23]  R. Wolfe,et al.  Role of insulin and glucagon in the response of glucose and alanine kinetics in burn-injured patients. , 1986, The Journal of clinical investigation.

[24]  J. McMurry,et al.  Wound healing with diabetes mellitus. Better glucose control for better wound healing in diabetes. , 1984, The Surgical clinics of North America.

[25]  R. Wolfe,et al.  Glucose metabolism in severely burned patients. , 1979, Metabolism: clinical and experimental.

[26]  A. Mason,et al.  Influence of the Burn Wound on Local and Systemic Responses to Injury , 1977, Annals of surgery.

[27]  L. Jorfeldt,et al.  Leg blood flow during exercise in man. , 1971, Clinical science.

[28]  E. Jéquier,et al.  Assessment of energy expenditure and fuel utilization in man. , 1987, Annual review of nutrition.

[29]  C. J. van Oss,et al.  Influence of intermittent hyperglycemic glucose levels on the phagocytosis of microorganisms by human granulocytes in vitro. , 1978, Immunological communications.