Practicalities of selenium supplementation in critically ill patients

被引:36
作者
Angstwurm, Matthias W. A. [1 ]
Gaertner, Roland [1 ]
机构
[1] Med Klin, Intens Care Unit, D-80336 Munich, Germany
关键词
adjuvant sepsis therapy; selenium supplementation; selenoenzymes;
D O I
10.1097/01.mco.0000222105.30795.7f
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review To review the reason for and clinical effects of selenium supplementation in critically ill patients. Recent findings Selenium-dependent enzymes and selenoprotein P regulate immune and endothelial cell function. Obviously not the anorganic compounds of selenium but the activity of selenium-dependent enzymes is the most important factor modulating the immune system and the clinical outcome of patients. Despite low selenium levels in severely ill patients and low glutathione peroxidase activity associated with the extent of multiorgan dysfunction, only a few trials have investigated the effect of selenium supplementation on clinical outcome. A metaanalysis did not reveal a statistically significant survival rate with selenium supplementation, but suggested a dose-dependent trend. The recently completed multicentre trial on high-dose selenium supplementation in septic patients also did not reveal a significant overall reduction in mortality. Summary The available evidence suggests that selenoproteins play an important role in the immunomodulation of critically ill patients and a sodium selenite supplementation upregulates these selenoenzymes. The intervention trials with sodium selenite performed to date are small and therefore only a tendency in reduction of morbidity and mortality could be demonstrated. Larger trials are necessary to show the supposed benefits and risks of selenite supplementation in critically ill patients.
引用
收藏
页码:233 / 238
页数:6
相关论文
共 83 条
[11]   Copper, selenium, zinc, and thiamine balances during continuous venovenous hemodiafiltration in critically ill patients [J].
Berger, MM ;
Shenkin, A ;
Revelly, JP ;
Roberts, E ;
Cayeux, MC ;
Baines, M ;
Chioléro, RL .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2004, 80 (02) :410-416
[12]   SELENIUM LOSSES IN 10 BURNED PATIENTS [J].
BERGER, MM ;
CAVADINI, C ;
BART, A ;
BLONDEL, A ;
BARTHOLDI, I ;
VANDERVALE, A ;
KRUPP, S ;
CHIOLERO, R ;
FREEMAN, J ;
DIRREN, H .
CLINICAL NUTRITION, 1992, 11 (02) :75-82
[13]   Insights into the hierarchy of selenium incorporation [J].
Berry, MJ .
NATURE GENETICS, 2005, 37 (11) :1162-1163
[14]   Time course of oxidative stress after major burns [J].
Bertin-Maghit, M ;
Goudable, J ;
Dalmas, E ;
Steghens, JP ;
Bouchard, C ;
Gueugniaud, PY ;
Petit, P ;
Delafosse, B .
INTENSIVE CARE MEDICINE, 2000, 26 (06) :800-803
[15]  
Broome CS, 2004, AM J CLIN NUTR, V80, P154
[16]   MOLECULAR-BIOLOGY OF SELENIUM WITH IMPLICATIONS FOR ITS METABOLISM [J].
BURK, RF .
FASEB JOURNAL, 1991, 5 (09) :2274-2279
[17]   Selenoprotein P associates with endothelial cells in rat tissues [J].
Burk, RF ;
Hill, KE ;
Boeglin, ME ;
Ebner, FF ;
Chittum, HS .
HISTOCHEMISTRY AND CELL BIOLOGY, 1997, 108 (01) :11-15
[18]   Specific excision of the selenocysteine tRNA[Ser]Sec (Trsp) gene in mouse liver demonstrates an essential role of selenoproteins in liver function [J].
Carlson, BA ;
Novoselov, SV ;
Kumaraswamy, E ;
Lee, BJ ;
Anver, MR ;
Gladyshev, VN ;
Hatfield, DL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (09) :8011-8017
[19]   Genetic variation in selenoprotein S influences inflammatory response [J].
Curran, JE ;
Jowett, JBM ;
Elliott, KS ;
Gao, Y ;
Gluschenko, K ;
Wang, JM ;
Azim, DMA ;
Cai, GW ;
Mahaney, MC ;
Comuzzie, AG ;
Dyer, TD ;
Walder, KR ;
Zimmet, P ;
MacCluer, JW ;
Collier, GR ;
Kissebah, AH ;
Blangero, J .
NATURE GENETICS, 2005, 37 (11) :1234-1241
[20]  
DAHER R, 1992, J TRACE ELEM ELECT H, V6, P189