Association between preoperative plasma sRAGE levels and recovery from cardiac surgery
Author(s)
Creagh-Brown, Benedict C
Quinlan, Gregory J
Hector, Lauren R
Evans, Timothy W
Burke-Gaffney, Anne
Type
Journal Article
Abstract
Background. The receptor for advanced glycation end products (RAGE) is an inflammation-perpetuating receptor, and soluble
RAGE (sRAGE) is a marker of cellular RAGE expression. This study investigated whether raised plasma levels prior to surgery of
sRAGE or S100A8/A9 (a RAGE ligand) were associated with longer duration of hospital care in patients undergoing cardiac surgery
necessitating cardiopulmonary bypass. Methods. Patients (𝑛 = 130) undergoing elective cardiac surgery were enrolled prospectively.
Plasma sRAGE and S100A8/A9 concentrations were measured before and 2 h after surgery. Results. Preoperative plasma sRAGE
increased significantly (𝑃 < 0.0001) from 1.06 ng/mL (IQR, 0.72–1.76) to 1.93 ng/mL (IQR, 1.14–2.63) 2 h postoperatively. Plasma
S100A8/9 was also significantly (𝑃 < 0.0001) higher 2 h postoperatively (2.37 𝜇g/mL, IQR, 1.81–3.05) compared to pre-operative
levels (0.41 𝜇g/mL, IQR, 0.2–0.65). Preoperative sRAGE, but not S100A8/A9, was positively and significantly correlated with
duration of critical illness (𝑟 = 0.3, 𝑃 = 0.0007) and length of hospital stay (LOS; 𝑟 = 0.31, 𝑃 < 0.0005). Multivariate binary
logistic regression showed preoperative sRAGE to be, statistically, an independent predictor of greater than median duration of
critical illness (odds ratio 16.6, 𝑃 = 0.014) and to be, statistically, the strongest independent predictor of hospital LOS. Conclusion.
Higher preoperative plasma sRAGE levels were associated with prolonged duration of care in adults undergoing cardiac surgery
requiring cardiopulmonary bypass.
RAGE (sRAGE) is a marker of cellular RAGE expression. This study investigated whether raised plasma levels prior to surgery of
sRAGE or S100A8/A9 (a RAGE ligand) were associated with longer duration of hospital care in patients undergoing cardiac surgery
necessitating cardiopulmonary bypass. Methods. Patients (𝑛 = 130) undergoing elective cardiac surgery were enrolled prospectively.
Plasma sRAGE and S100A8/A9 concentrations were measured before and 2 h after surgery. Results. Preoperative plasma sRAGE
increased significantly (𝑃 < 0.0001) from 1.06 ng/mL (IQR, 0.72–1.76) to 1.93 ng/mL (IQR, 1.14–2.63) 2 h postoperatively. Plasma
S100A8/9 was also significantly (𝑃 < 0.0001) higher 2 h postoperatively (2.37 𝜇g/mL, IQR, 1.81–3.05) compared to pre-operative
levels (0.41 𝜇g/mL, IQR, 0.2–0.65). Preoperative sRAGE, but not S100A8/A9, was positively and significantly correlated with
duration of critical illness (𝑟 = 0.3, 𝑃 = 0.0007) and length of hospital stay (LOS; 𝑟 = 0.31, 𝑃 < 0.0005). Multivariate binary
logistic regression showed preoperative sRAGE to be, statistically, an independent predictor of greater than median duration of
critical illness (odds ratio 16.6, 𝑃 = 0.014) and to be, statistically, the strongest independent predictor of hospital LOS. Conclusion.
Higher preoperative plasma sRAGE levels were associated with prolonged duration of care in adults undergoing cardiac surgery
requiring cardiopulmonary bypass.
Date Issued
2013-09-05
Date Acceptance
2013-08-01
Citation
Mediators of Inflammation, 2013, 2013, pp.1-7
ISSN
0962-9351
Publisher
Hindawi Publishing Corporation
Start Page
1
End Page
7
Journal / Book Title
Mediators of Inflammation
Volume
2013
Copyright Statement
© 2013 Benedict C. Creagh-Brown et al. This is an open access article distributed under the Creative Commons
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is
properly cited.
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is
properly cited.
License URL
Sponsor
Dunhill Medical Trust
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000324425500001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
R421E/1114
Subjects
Science & Technology
Life Sciences & Biomedicine
Cell Biology
Immunology
GLYCATION END-PRODUCTS
INTENSIVE-CARE-UNIT
INFLAMMATORY RESPONSE
RISK-FACTORS
RECEPTOR
S100A9
STAY
ACTIVATION
INFECTION
BYPASS
Publication Status
Published
Article Number
ARTN 496031
Date Publish Online
2013-09-05