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https://hdl.handle.net/20.500.14279/1179
Title: | Association of proinflammatory molecules with apoptotic markers and survival in critically ill multiple organ dysfunction patients | Authors: | Papathanassoglou, Elizabeth Moynihan, Jan Dafni, Ourania Mantzoros, Christos S. Ackerman, Michael John |
Major Field of Science: | Medical and Health Sciences | Field Category: | Health Sciences | Keywords: | MODS;Apoptosis;Fas;Cytokines;Nitric oxide;Cortisol;Interleukin-6;Tumor necrosis factor-α | Issue Date: | 1-Oct-2003 | Source: | Biological Research for Nursing, 2003, vol. 5, no. 2, pp. 129-141 | Volume: | 5 | Issue: | 2 | Start page: | 129 | End page: | 141 | Journal: | Biological Research for Nursing | Abstract: | Recent evidence supports the involvement of apoptosis in multiple organ dysfunction (MODS). The authors examined the hypothesis that nitric oxide (NO), interleukin (IL)-6, tumor necrosis factor (TNF)-α, and cortisol correlate with Fas and Fas ligand (FasL) expression on peripheral blood mononuclear cells and that Fas and FasL, therefore, mediate their association with MODS severity. Thirty-five critically ill adult MODS patients were followed for up to 14 days and were compared to non-MODS matched controls. Fas, FasL, nitrate, cortisol, and IL-6 were elevated in MODS patients (P < 0.05). Nitrate and cortisol correlated with Fas expression (P < 0.05). All factors studied, except for TNF-α, correlated with MODS severity (P< 0.05); however, by multivariate analyses, Fas and FasL were independently associated with severity and survival (P < 0.05). The inflammatory molecules studied may mediate the association of apoptotic constituents with MODS severity and survival only in part. | URI: | https://hdl.handle.net/20.500.14279/1179 | ISSN: | 15524175 | DOI: | 10.1177/1099800403257189 | Rights: | © Sage Publications | Type: | Article | Affiliation : | National and Kapodistrian University of Athens University of Rochester Harvard University |
Publication Type: | Peer Reviewed |
Appears in Collections: | Άρθρα/Articles |
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