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Plasma soluble e-selectin in necrotising enterocolitis

Plasma soluble e-selectin in necrotising enterocolitis
Plasma soluble e-selectin in necrotising enterocolitis
Aim: E-selectin is an important mediator of leukocyte-endothelial adhesion. It is expressed on activated endothelium, and shed into the circulation in its soluble form. In babies with necrotising enterocolitis (NEC), increased intestinal expression of E-selectin has been associated with multiple organ failure and an adverse outcome. The aim of this study was to determine whether increased circulating soluble E-selectin (sE-selectin) was associated with a worse prognosis.

Methods: With ethical approval, plasma samples from 20 infants with Bell stage II and III NEC were analysed. Both pre- and postoperative samples were available in 6 infants. The severity of illness was assessed using a sequential organ failure assessment score (SOFA) specifically designed for use in NEC. Plasma concentration of sE-selectin was determined by ELISA. Data, which were not normally distributed, were compared by Spearman's rank correlation coefficient and Wilcoxon signed rank test.

Results: Plasma sE-selectin was strongly negatively correlated with corrected gestational age at the time of sampling (r?=???0.425, p?=?0.006). There was no association between plasma sE-selectin and outcome (death or survival to discharge), severity of intestinal disease (focal, multifocal or pan-intestinal), or SOFA score. Surgery for suspected perforation, however, caused a significant elevation in sE-selectin levels (p?=?0.031).

Conclusions: Plasma sE-selectin, a described marker of endothelial activation, is increased following surgery for NEC. However, prematurity appears to be the cause of an increase in sE-selectin level, confounding the potential use of sE-selectin levels as a predictor of severity of illness in NEC.
necrotising enterocolitis, adhesion molecules, e?selectin, inflammation
0939-7248
419-422
Khoo, A.K.
3f4e12e5-05eb-4c3b-909f-179e99d7785b
Hall, N.J.
6919e8af-3890-42c1-98a7-c110791957cf
Alexander, N.
c72a655d-88d9-4d7d-9e99-402076248b5d
Evennett, N.J.
68ddc886-e351-489f-b19b-04ccfc3a193d
Pierro, A.
cef08d1c-bb0b-42ba-85ce-32d9a85c04a8
Eaton, S.
77a21196-4388-442f-9306-3a013b8b1259
Khoo, A.K.
3f4e12e5-05eb-4c3b-909f-179e99d7785b
Hall, N.J.
6919e8af-3890-42c1-98a7-c110791957cf
Alexander, N.
c72a655d-88d9-4d7d-9e99-402076248b5d
Evennett, N.J.
68ddc886-e351-489f-b19b-04ccfc3a193d
Pierro, A.
cef08d1c-bb0b-42ba-85ce-32d9a85c04a8
Eaton, S.
77a21196-4388-442f-9306-3a013b8b1259

Khoo, A.K., Hall, N.J., Alexander, N., Evennett, N.J., Pierro, A. and Eaton, S. (2008) Plasma soluble e-selectin in necrotising enterocolitis. European Journal of Pediatric Surgery, 18 (6), 419-422. (doi:10.1055/s-2008-1038908). (PMID:19012233)

Record type: Article

Abstract

Aim: E-selectin is an important mediator of leukocyte-endothelial adhesion. It is expressed on activated endothelium, and shed into the circulation in its soluble form. In babies with necrotising enterocolitis (NEC), increased intestinal expression of E-selectin has been associated with multiple organ failure and an adverse outcome. The aim of this study was to determine whether increased circulating soluble E-selectin (sE-selectin) was associated with a worse prognosis.

Methods: With ethical approval, plasma samples from 20 infants with Bell stage II and III NEC were analysed. Both pre- and postoperative samples were available in 6 infants. The severity of illness was assessed using a sequential organ failure assessment score (SOFA) specifically designed for use in NEC. Plasma concentration of sE-selectin was determined by ELISA. Data, which were not normally distributed, were compared by Spearman's rank correlation coefficient and Wilcoxon signed rank test.

Results: Plasma sE-selectin was strongly negatively correlated with corrected gestational age at the time of sampling (r?=???0.425, p?=?0.006). There was no association between plasma sE-selectin and outcome (death or survival to discharge), severity of intestinal disease (focal, multifocal or pan-intestinal), or SOFA score. Surgery for suspected perforation, however, caused a significant elevation in sE-selectin levels (p?=?0.031).

Conclusions: Plasma sE-selectin, a described marker of endothelial activation, is increased following surgery for NEC. However, prematurity appears to be the cause of an increase in sE-selectin level, confounding the potential use of sE-selectin levels as a predictor of severity of illness in NEC.

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More information

Published date: December 2008
Keywords: necrotising enterocolitis, adhesion molecules, e?selectin, inflammation
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 378470
URI: http://eprints.soton.ac.uk/id/eprint/378470
ISSN: 0939-7248
PURE UUID: 4f0becb1-c26b-4467-8ce7-b83ac63ac8ef
ORCID for N.J. Hall: ORCID iD orcid.org/0000-0001-8570-9374

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Date deposited: 07 Jul 2015 16:24
Last modified: 15 Mar 2024 03:38

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Contributors

Author: A.K. Khoo
Author: N.J. Hall ORCID iD
Author: N. Alexander
Author: N.J. Evennett
Author: A. Pierro
Author: S. Eaton

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