Glutamine: role in critical illness and ongoing clinical trials

被引:85
作者
Wischmeyer, Paul E. [1 ,2 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Anesthesiol, Aurora, CO 80045 USA
[2] Nutr Support Serv, Aurora, CO 80045 USA
关键词
head injury; heat shock protein; insulin resistance; molecular mechanism; mortality; nutritional pharmacology;
D O I
10.1097/MOG.0b013e3282f4db94
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review This review will assess recent clinical and mechanistic data examining glutamine's ability to reduce morbidity and mortality in critical illness. Recent findings Updated metaanalysis data reveal a significant benefit of glutamine supplementation on mortality, length of stay, and infectious morbidity in critical illness. Recent data support glutamine's use in critically ill patients requiring parenteral nutrition and new data reveal safety and efficacy in head-injured patients. Further, new findings on glutamine's beneficial effect on insulin resistance in critical illness will be reviewed. Recent laboratory data have clarified a number of key mechanistic pathways by which glutamine may improve outcome in critical illness. Summary Severe glutamine deficiencies occur rapidly in critical illness. The magnitude of glutamine deficiency is correlated with ICU mortality. Further, metaanalysis reveals glutamine reduces morbidity and mortality in critical illness. It is likely that our new understanding of the molecular pathways by which glutamine acts will lead to insight on how best to utilize glutamine as a nutritional therapy. Presently, randomized, multicenter clinical trials utilizing glutamine as both nutritional replacement and pharmacologic intervention, independent of nutritional needs, are ongoing.
引用
收藏
页码:190 / 197
页数:8
相关论文
共 53 条
[1]  
ANDREWS PJ, 2007, TRIALS, V2007, P8
[2]   Parenterally administered dipeptide alanyl-glutamine prevents worsening of insulin sensitivity in multiple-trauma patients [J].
Bakalar, B ;
Duska, F ;
Pachl, J ;
Fric, M ;
Otahal, M ;
Pazout, J ;
Andel, M .
CRITICAL CARE MEDICINE, 2006, 34 (02) :381-386
[3]   Intravenous glutamine supplementation to head trauma patients leaves cerebral glutamate concentration unaffected [J].
Berg, A. ;
Bellander, B. M. ;
Wanecek, M. ;
Gamrin, L. ;
Elving, Ase ;
Rooyackers, O. ;
Ungerstedt, U. ;
Wernerman, J. .
INTENSIVE CARE MEDICINE, 2006, 32 (11) :1741-1746
[4]   Glutamine, gene expression, and cell function [J].
Curi, Rui ;
Newsholme, Philip ;
Procopio, Joaquim ;
Lagranha, Claudia ;
Gorjao, Renata ;
Pithon-Curi, Tania Cristina .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2007, 12 :344-357
[5]   Intestinal permeability and systemic infections in critically ill patients: Effect of glutamine [J].
De-Souza, DA ;
Greene, LJ .
CRITICAL CARE MEDICINE, 2005, 33 (05) :1125-1135
[6]   L-alanyl-L-glutamine dipeptide-supplemented total parenteral nutrition reduces infectious complications and glucose intolerance in critically ill patients:: The French controlled, randomized, double-blind, multicenter study [J].
Déchelotte, P ;
Hasselmann, M ;
Cynober, L ;
Allaouchiche, B ;
Coëffier, M ;
Hecketsweiler, B ;
Merle, V ;
Mazerolles, M ;
Samba, D ;
Guillou, YM ;
Petit, J ;
Mansoor, O ;
Colas, G ;
Cohendy, R ;
Barnoud, D ;
Czernichow, P ;
Bleichner, G .
CRITICAL CARE MEDICINE, 2006, 34 (03) :598-604
[7]   Rapid increase in hospitalization and mortality rates for severe sepsis in the United States: A trend analysis from 1993 to 2003 [J].
Dombrovskiy, Viktor Y. ;
Martin, Andrew A. ;
Sunderram, Jagadeeshan ;
Paz, Harold L. .
CRITICAL CARE MEDICINE, 2007, 35 (05) :1244-1250
[8]   Glutamine inhibits cytokine-induced apoptosis in human colonic epithelial cells via the pyrimidine pathway [J].
Evans, ME ;
Jones, DP ;
Ziegler, TR .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (03) :G388-G396
[9]   Cytopathic hypoxia - Is oxygen use impaired in sepsis as a result of an acquired intrinsic derangement in cellular respiration? [J].
Fink, MP .
CRITICAL CARE CLINICS, 2002, 18 (01) :165-+
[10]   A descriptive study of skeletal muscle metabolism in critically ill patients: Free amino acids, energy-rich phosphates, protein, nucleic acids, fat, water, and electrolytes [J].
Gamrin, L ;
Essen, P ;
Forsberg, AM ;
Hultman, E ;
Wernerman, J .
CRITICAL CARE MEDICINE, 1996, 24 (04) :575-583