<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(5)</volume><submitter>Hastbacka J</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Matrix metalloproteinases (MMPs) -8 and -9 are released from neutrophils in acute inflammation and may contribute to permeability changes in burn injury. In retrospective studies on sepsis, levels of MMP-8, MMP-9, and tissue inhibitor of metalloproteinase-1 (TIMP-1) differed from those of healthy controls, and TIMP-1 showed an association with outcome. Our objective was to investigate the relationship between these proteins and disease severity and outcome in burn patients.&lt;h4>Methods&lt;/h4>In this prospective, observational, two-center study, we collected plasma samples from admission to day 21 post-burn, and burn blister fluid samples on admission. We compared MMP-8, -9, and TIMP-1 levels between TBSA&lt;20% (N = 19) and TBSA>20% (N = 30) injured patients and healthy controls, and between 90-day survivors and non-survivors. MMP-8, -9, and TIMP-1 levels at 24-48 hours from injury, their maximal levels, and their time-adjusted means were compared between groups. Correlations with clinical parameters and the extent of burn were analyzed. MMP-8, -9, and TIMP-1 levels in burn blister fluids were also studied.&lt;h4>Results&lt;/h4>Plasma MMP-8 and -9 were higher in patients than in healthy controls (P&lt;0.001 and P = 0.016), but only MMP-8 differed between the TBSA&lt;20% and TBSA>20% groups. MMP-8 and -9 were not associated with clinical severity or outcome measures. TIMP-1 differed significantly between patients and controls (P&lt;0.001) and between TBSA&lt;20% and TBSA>20% groups (P&lt;0.002). TIMP-1 was associated with 90-day mortality and correlated with the extent of injury and clinical measures of disease severity. TIMP-1 may serve as a new biomarker in outcome prognostication of burn patients.</pubmed_abstract><journal>PloS one</journal><pagination>e0125918</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4422709</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Matrix metalloproteinases -8 and -9 and tissue inhibitor of metalloproteinase-1 in burn patients. A prospective observational study.</pubmed_title><pmcid>PMC4422709</pmcid><pubmed_authors>Hastbacka J</pubmed_authors><pubmed_authors>Huss F</pubmed_authors><pubmed_authors>Hult M</pubmed_authors><pubmed_authors>Vuola J</pubmed_authors><pubmed_authors>Sorsa T</pubmed_authors><pubmed_authors>Freden F</pubmed_authors><pubmed_authors>Wilkman E</pubmed_authors><pubmed_authors>Bergquist M</pubmed_authors><pubmed_authors>Tervahartiala T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Matrix metalloproteinases -8 and -9 and tissue inhibitor of metalloproteinase-1 in burn patients. A prospective observational study.</name><description>&lt;h4>Introduction&lt;/h4>Matrix metalloproteinases (MMPs) -8 and -9 are released from neutrophils in acute inflammation and may contribute to permeability changes in burn injury. In retrospective studies on sepsis, levels of MMP-8, MMP-9, and tissue inhibitor of metalloproteinase-1 (TIMP-1) differed from those of healthy controls, and TIMP-1 showed an association with outcome. Our objective was to investigate the relationship between these proteins and disease severity and outcome in burn patients.&lt;h4>Methods&lt;/h4>In this prospective, observational, two-center study, we collected plasma samples from admission to day 21 post-burn, and burn blister fluid samples on admission. We compared MMP-8, -9, and TIMP-1 levels between TBSA&lt;20% (N = 19) and TBSA>20% (N = 30) injured patients and healthy controls, and between 90-day survivors and non-survivors. MMP-8, -9, and TIMP-1 levels at 24-48 hours from injury, their maximal levels, and their time-adjusted means were compared between groups. Correlations with clinical parameters and the extent of burn were analyzed. MMP-8, -9, and TIMP-1 levels in burn blister fluids were also studied.&lt;h4>Results&lt;/h4>Plasma MMP-8 and -9 were higher in patients than in healthy controls (P&lt;0.001 and P = 0.016), but only MMP-8 differed between the TBSA&lt;20% and TBSA>20% groups. MMP-8 and -9 were not associated with clinical severity or outcome measures. TIMP-1 differed significantly between patients and controls (P&lt;0.001) and between TBSA&lt;20% and TBSA>20% groups (P&lt;0.002). TIMP-1 was associated with 90-day mortality and correlated with the extent of injury and clinical measures of disease severity. TIMP-1 may serve as a new biomarker in outcome prognostication of burn patients.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2021-02-20T15:21:16Z</modification><creation>2019-03-26T23:32:33Z</creation></dates><accession>S-EPMC4422709</accession><cross_references><pubmed>25945788</pubmed><doi>10.1371/journal.pone.0125918</doi></cross_references></HashMap>