PMID- 31764620 OWN - NLM STAT- MEDLINE DCOM- 20210514 LR - 20210514 IS - 1540-0514 (Electronic) IS - 1073-2322 (Linking) VI - 54 IP - 1 DP - 2020 Jul TI - Tenascin C Plasma Levels in Critically Ill Patients with or Without Sepsis: A Multicenter Observational Study. PG - 62-69 LID - 10.1097/SHK.0000000000001481 [doi] AB - Tenascin C (TNC) is an extracellular matrix protein able to modulate the immune response. Knowledge regarding its role during sepsis and general critical illness is still limited. We here assessed the temporal dynamics of plasma TNC during sepsis and nonseptic critical illness, its capacity to predict patient outcome, and its specificity toward infection. TNC plasma concentrations were measured in 895 consecutive sepsis patients on ICU admission, day 2 and 4 thereafter, and, in a subset, before ICU discharge. To assess TNC diagnostic value, we compared patients with abdominal sepsis (N = 143) to noninfectious abdominal surgery controls (N = 98), and patients with severe community-acquired pneumonia (CAP, N = 227) to patients whose CAP diagnosis was retrospectively refuted (no-CAP controls, N = 70). Plasma TNC levels were persistently elevated in sepsis patients compared with healthy volunteers throughout the ICU stay. TNC levels varied by the site of infection and increased with the number of organs failing. Association of TNC levels with 30-day mortality could be wholly attributed to differences in disease severity. Noninfectious ICU patients also showed elevated TNC levels, albeit with different temporal dynamics. Although admission TNC was higher in CAP than in no-CAP patients, it performed poorly in distinguishing the 2 groups.TNC plasma levels are persistently elevated during sepsis and nonseptic critical illness. In sepsis patients, they are reflective of disease severity more than independent predictors of mortality. Despite higher levels in patients with infection compared with noninfectious controls, TNC does not perform sufficiently to be used as a standalone biomarker discriminating sepsis from noninfectious critical illness. FAU - Meijer, Mariska T AU - Meijer MT AD - Center for Experimental and Molecular Medicine, Amsterdam University Medical Centers, Academic Medical Center, University of Amsterdam. AD - Amsterdam Institute for Infection and Immunity, Amsterdam University Medical Centers, Amsterdam. FAU - Uhel, Fabrice AU - Uhel F AD - Center for Experimental and Molecular Medicine, Amsterdam University Medical Centers, Academic Medical Center, University of Amsterdam. AD - Amsterdam Institute for Infection and Immunity, Amsterdam University Medical Centers, Amsterdam. FAU - Cremer, Olaf L AU - Cremer OL AD - Department of Intensive Care Medicine, University Medical Center Utrecht, Utrecht. FAU - Schultz, Marcus J AU - Schultz MJ AD - Department of Intensive Care. FAU - van der Poll, Tom AU - van der Poll T AD - Center for Experimental and Molecular Medicine, Amsterdam University Medical Centers, Academic Medical Center, University of Amsterdam. AD - Amsterdam Institute for Infection and Immunity, Amsterdam University Medical Centers, Amsterdam. AD - Division of Infectious Diseases, Amsterdam University Medical Centers, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands. CN - MARS consortium LA - eng PT - Clinical Trial PT - Journal Article PT - Multicenter Study PT - Observational Study PT - Research Support, Non-U.S. Gov't PL - United States TA - Shock JT - Shock (Augusta, Ga.) JID - 9421564 RN - 0 (Biomarkers) RN - 0 (TNC protein, human) RN - 0 (Tenascin) SB - IM MH - Aged MH - Biomarkers/blood MH - Case-Control Studies MH - *Critical Illness/mortality MH - Female MH - Humans MH - Intensive Care Units/statistics & numerical data MH - Male MH - Middle Aged MH - Sepsis/*blood/mortality MH - Severity of Illness Index MH - Tenascin/*blood EDAT- 2019/11/26 06:00 MHDA- 2021/05/15 06:00 CRDT- 2019/11/26 06:00 PHST- 2019/11/26 06:00 [pubmed] PHST- 2021/05/15 06:00 [medline] PHST- 2019/11/26 06:00 [entrez] AID - 00024382-202007000-00011 [pii] AID - 10.1097/SHK.0000000000001481 [doi] PST - ppublish SO - Shock. 2020 Jul;54(1):62-69. doi: 10.1097/SHK.0000000000001481.