TY - JOUR
T1 - Serum levels of osteopontin are increased in SIRS and sepsis
AU - VASCHETTO, Rosanna
AU - Nicola, S
AU - Olivieri, C
AU - Boggio, E
AU - Piccolella, F
AU - Mesturini, R
AU - Damnotti, F
AU - Colombo, D
AU - Navalesi, P
AU - DELLA CORTE, Francesco
AU - DIANZANI, Umberto
AU - CHIOCCHETTI, Annalisa
N1 - Funding Information:
Acknowledgments This work was partially supported by Telethon grant E1170 (Rome), AIRC (Milan), PRIN Project (MIUR, Rome), Compagnia di San Paolo (Turin), Regione Piemonte (Ricerca Sanitaria Finalizzata Project and Ricerca Sanitaria Applicata-CIPE Project), FISM 2005/R/10 (Genoa), Ricerca Corrente Ministeriale (Rome), Fondazione CARIPLO (Milan).
PY - 2008
Y1 - 2008
N2 - Objective: In sepsis, dysregulation of the immune response leads to rapid multiorgan failure and death. Accurate and timely diagnosis is lifesaving and should discriminate sepsis from the systemic inflammatory response syndrome (SIRS) caused by non-infectious agents. Osteopontin acts as an extracellular matrix component or a soluble cytokine in inflamed tissues. Its exact role in immune response and sepsis remains to be elucidated. Therefore, we investigated the role of osteopontin in SIRS and sepsis. Design: Prospective, observational study. Setting: Intensive care unit of a university hospital. Patients and participants: Fifty-six patients with SIRS or sepsis and 56 healthy subjects were enrolled. Interventions: We analyzed the serum levels of osteopontin and TH1- TH2 cytokines and investigated the role of osteopontin on interleukin 6 secretion by monocytes. Measurements and main results: Serum osteopontin levels were strikingly higher in patients than in controls and in sepsis than in SIRS, and decreased during the resolution of both the disorders. Receiver operating characteristic curves showed that osteopontin levels have discriminative power between SIRS and sepsis with an area under the curve of 0.796. Osteopontin levels directly correlated with those of interleukin 6 and in vitro, recombinant osteopontin increased interleukin 6 secretion by monocytes in both the absence and presence of high doses of lipopolysaccharide. Conclusion: These data suggest that osteopontin might be a mediator involved in the pathogenesis of SIRS and sepsis, possibly by supporting interleukin 6 secretion.
AB - Objective: In sepsis, dysregulation of the immune response leads to rapid multiorgan failure and death. Accurate and timely diagnosis is lifesaving and should discriminate sepsis from the systemic inflammatory response syndrome (SIRS) caused by non-infectious agents. Osteopontin acts as an extracellular matrix component or a soluble cytokine in inflamed tissues. Its exact role in immune response and sepsis remains to be elucidated. Therefore, we investigated the role of osteopontin in SIRS and sepsis. Design: Prospective, observational study. Setting: Intensive care unit of a university hospital. Patients and participants: Fifty-six patients with SIRS or sepsis and 56 healthy subjects were enrolled. Interventions: We analyzed the serum levels of osteopontin and TH1- TH2 cytokines and investigated the role of osteopontin on interleukin 6 secretion by monocytes. Measurements and main results: Serum osteopontin levels were strikingly higher in patients than in controls and in sepsis than in SIRS, and decreased during the resolution of both the disorders. Receiver operating characteristic curves showed that osteopontin levels have discriminative power between SIRS and sepsis with an area under the curve of 0.796. Osteopontin levels directly correlated with those of interleukin 6 and in vitro, recombinant osteopontin increased interleukin 6 secretion by monocytes in both the absence and presence of high doses of lipopolysaccharide. Conclusion: These data suggest that osteopontin might be a mediator involved in the pathogenesis of SIRS and sepsis, possibly by supporting interleukin 6 secretion.
UR - https://iris.uniupo.it/handle/11579/29270
U2 - 10.1007/s00134-008-1268-4
DO - 10.1007/s00134-008-1268-4
M3 - Article
SN - 0342-4642
VL - 34
SP - 2176
EP - 2184
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 12
ER -