l-Selectin shows time and gender dependency in association with MODS
Background: Recent investigations have demonstrated gender related immunologic alterations after trauma. These complications arise due to polymorphonuclear granulocytes (PMN) interacting with endothelium via l-selectin. Therefore, the purpose of this study was to investigate gender related differenc...
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Veröffentlicht in: | Injury 2004-11, Vol.35 (11), p.1087-1095 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background: Recent investigations have demonstrated gender related immunologic alterations after trauma. These complications arise due to polymorphonuclear granulocytes (PMN) interacting with endothelium via
l-selectin. Therefore, the purpose of this study was to investigate gender related differences in the expression of
l-selectin in relation to posttraumatic multiple organ dysfunction syndrome (MODS).
Methods: Multiply injured patients were prospectively entered in the study. MODS was determined using the Denver score. The concentration of
l-selectin on the surface of PMN was determined using flow cytometry during a 14 days’ period.
Results: 48 patients were included in the study. The kinetics of
l-selectin were different comparing male and female patients. Male patients with MODS initially showed a rapid decrease of surface
l-selectin from 80 to 20
ng/ml. A return to admission levels was related to MODS. Male patients without MODS displayed elevated
l-selectin levels up to 140
ng/ml. Female patients, however, all showed an initial rapid decrease of
l-selectin to 20
ng/ml. Women who developed posttraumatic MODS had significantly increased levels up to 110
ng/ml before development of MODS developed.
Conclusions: We feel that a gender related dimorphism in the initial
l-selectin expression following trauma exists and is associated with MODS. These findings indicate new therapeutic means for the treatment of MODS. Therapies should be timely and gender dependently coordinated. |
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ISSN: | 0020-1383 1879-0267 |
DOI: | 10.1016/j.injury.2004.03.014 |