Literature DB >> 29997296

Circulating RIPK3 levels are associated with mortality and organ failure during critical illness.

Kevin C Ma1,2, Edward J Schenck1,2, Ilias I Siempos1, Suzanne M Cloonan1, Eli J Finkelsztein1, Maria A Pabon1,3, Clara Oromendia4, Karla V Ballman4, Rebecca M Baron5, Laura E Fredenburgh5, Angelica Higuera5, Jin Young Lee6, Chi Ryang Chung6, Kyeongman Jeon6, Jeong Hoon Yang6, Judie A Howrylak7, Jin-Won Huh8, Gee Young Suh6, Augustine Mk Choi1,2.   

Abstract

BACKGROUND: Necroptosis is a form of programmed necrotic cell death that is rapidly emerging as an important pathophysiological pathway in numerous disease states. Necroptosis is dependent on receptor-interacting protein kinase 3 (RIPK3), a protein shown to play an important role in experimental models of critical illness. However, there is limited clinical evidence regarding the role of extracellular RIPK3 in human critical illness.
METHODS: Plasma RIPK3 levels were measured in 953 patients prospectively enrolled in 5 ongoing intensive care unit (ICU) cohorts in both the USA and Korea. RIPK3 concentrations among groups were compared using prospectively collected phenotypic and outcomes data.
RESULTS: In all 5 cohorts, extracellular RIPK3 levels in the plasma were higher in patients who died in the hospital compared with those who survived to discharge. In a combined analysis, increasing RIPK3 levels were associated with elevated odds of in-hospital mortality (odds ratio [OR] 1.7 for each log10-unit increase in RIPK3 level, P < 0.0001). When adjusted for baseline severity of illness, the OR for in-hospital mortality remained statistically significant (OR 1.33, P = 0.007). Higher RIPK3 levels were also associated with more severe organ failure.
CONCLUSIONS: Our findings suggest that elevated levels of RIPK3 in the plasma of patients admitted to the ICU are associated with in-hospital mortality and organ failure. FUNDING: Supported by NIH grants P01 HL108801, R01 HL079904, R01 HL055330, R01 HL060234, K99 HL125899, and KL2TR000458-10. Supported by Samsung Medical Center grant SMX1161431.

Entities:  

Keywords:  Apoptosis survival pathways; Inflammation; Innate immunity

Mesh:

Substances:

Year:  2018        PMID: 29997296      PMCID: PMC6124535          DOI: 10.1172/jci.insight.99692

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


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