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Systemic matrix metalloproteinase‐8 and tissue inhibitor of metalloproteinases‐1 levels in severe sepsis‐associated coagulopathy
Author(s) -
SIVULA M.,
HÄSTBACKA J.,
KUITUNEN A.,
LASSILA R.,
TERVAHARTIALA T.,
SORSA T.,
PETTILÄ V.
Publication year - 2015
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1111/aas.12423
Subject(s) - medicine , coagulopathy , disseminated intravascular coagulation , sepsis , gastroenterology , matrix metalloproteinase , pathogenesis , coagulation , prospective cohort study , matrix metalloproteinase 9 , coagulation testing , immunology
Background Matrix metalloproteinase‐8 ( MMP ‐8) and tissue inhibitor of metalloproteinases‐1 ( TIMP ‐1) have recently been suggested to be involved in coagulation process. Our objectives were to observe systemic MMP ‐8 and TIMP ‐1 levels in patients with severe sepsis with or without disseminated intravascular coagulation ( DIC ) and to study their relationship with coagulation markers over time. Methods Our prospective pilot study included 22 patients with severe sepsis, nine (41%) of whom had overt DIC . We analysed MMP ‐8 and TIMP ‐1 serum concentrations by time‐resolved immunofluorometric and enzyme‐linked immunosorbent assays, respectively, on days 1, 2, 4 and 7 after the intensive care unit admission. Traditional coagulation tests were taken at the same time points. The results were compared between patients with and without DIC . Blood samples from 10 healthy volunteers were used to demonstrate normal levels. Results Both patient groups had elevated levels of MMP ‐8 and TIMP ‐1 as compared with healthy controls. TIMP ‐1 concentration was almost twofold in DIC patients compared with those without DIC on the first 2 days. MMP ‐8 was elevated only on day 2. TIMP ‐1 correlated positively with the severity of coagulation disturbance and with disease severity scores. MMP ‐8 correlated negatively only with platelet count. Conclusion In this first human study, we could show that TIMP ‐1 is elevated in the early phase of sepsis‐induced overt DIC , and it correlates both with degree of coagulopathy and disease severity. These findings suggest that TIMP ‐1 may play a role in the pathogenesis of DIC in septic patients.