Endogenous carbon monoxide production correlates weakly with severity of acute illness

被引:20
作者
Scharte, M [1 ]
von Ostrowski, TA [1 ]
Daudel, E [1 ]
Freise, H [1 ]
Van Aken, H [1 ]
Bone, HG [1 ]
机构
[1] Univ Klinikum Munster, Klin & Poliklin Anasthesiol & Operat Intensivmed, Munster, Germany
关键词
carbon monoxide; endogenous production; critical illness; haeme oxygenase-1; multiple organ failure; inflammation;
D O I
10.1017/S0265021505002012
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background and objective: The enzyme haeme oxygenase(-1) is highly inducible by oxidative agents. Its product carbon monoxide is thought to exert anti-inflammatory properties. We recently showed, that critically ill patients produce higher amounts of carbon monoxide compared to healthy controls. In the present study we compare endogenous carbon monoxide production with the severity of illness of intensive care unit patients. Methods: Exhaled carbon monoxide concentration was measured in 95 mechanically ventilated, critically ill patients (mean age +/- SD, 59.5 +/- 15.7) on a carbon monoxide monitor. Measurements were taken every hour for 24 h in each patient. Data were analysed using Mann-Whitney rank sum test. Correlation analysis was performed with the Spearman's rank order correlation. Results: Carbon monoxide production correlated weakly with the multiple organ dysfunction score (R = 0.27; P = 0.009). Patients suffering from cardiac disease (median 22.5, interquartile range 16.2-27.4 mu L kg(-1) h(-1), vs. median 18.2, interquartile range 14.2-21.8 mu L kg(-1) h(-1), P = 0.008) and critically ill patients undergoing dialysis (median 25.0, interquartile range 21.4-30.2 mu L kg(-1) h(-1), vs. median 19.4, interquartile range 14.7-23.3 mu L kg(-1) h(-1), P = 0.004) produced significantly higher amounts of carbon monoxide compared to critically ill controls. Conclusion: The findings suggest that endogenous carbon monoxide production might reflect the severity of acute organ dysfunction.
引用
收藏
页码:117 / 122
页数:6
相关论文
共 36 条
[31]   Different faces of the heme-heme oxygenase system in inflammation [J].
Wagener, FADTG ;
Volk, HD ;
Willis, D ;
Abraham, NG ;
Soares, MP ;
Adema, GJ ;
Figdor, CG .
PHARMACOLOGICAL REVIEWS, 2003, 55 (03) :551-571
[32]   Heme is a potent inducer of inflammation in mice and is counteracted by heme oxygenase [J].
Wagener, FADTG ;
Eggert, A ;
Boerman, OC ;
Oyen, WJG ;
Verhofstad, A ;
Abraham, NG ;
Adema, G ;
van Kooyk, Y ;
de Witte, T ;
Figdor, CG .
BLOOD, 2001, 98 (06) :1802-1811
[33]   Increased carbon monoxide in exhaled air of subjects with upper respiratory tract infections [J].
Yamaya, M ;
Sekizawa, K ;
Ishizuka, S ;
Monma, M ;
Mizuta, K ;
Sasaki, H .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (01) :311-314
[34]   Increased carbon monoxide in exhaled air of asthmatic patients [J].
Zayasu, K ;
Sekizawa, K ;
Okinaga, S ;
Yamaya, M ;
Ohrui, T ;
Sasaki, H .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (04) :1140-1143
[35]   Increased endogenous carbon monoxide production in severe sepsis [J].
Zegdi, R ;
Perrin, D ;
Burdin, M ;
Boiteau, R ;
Tenaillon, A .
INTENSIVE CARE MEDICINE, 2002, 28 (06) :793-796
[36]   Carbon monoxide modulates Fas/Fas ligand, caspases, and Bcl-2 family proteins via the p38α mitogen-activated protein kinase pathway during ischemia-reperfusion lung injury [J].
Zhang, XC ;
Shan, PY ;
Alam, J ;
Davis, RJ ;
Flavell, RA ;
Lee, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :22061-22070