Identification of Clinically Significant Cytokine Signature Clusters in Patients With Septic Shock

Author:

Zhao Jack O.1,Patel Bhakti K.1,Krishack Paulette1,Stutz Matthew R.1,Pearson Steven D.1,Lin Julie2,Lecompte-Osorio Paola A.1,Dugan Karen C.3,Kim Seoyoen1,Gras Nicole1,Pohlman Anne1,Kress John P.1,Hall Jesse B.1,Sperling Anne I.4,Adegunsoye Ayodeji1,Verhoef Philip A.5,Wolfe Krysta S.1

Affiliation:

1. Pulmonary and Critical Care, University of Chicago Medical Center, Chicago, IL.

2. Pulmonary Medicine, MD Anderson Cancer Center, The University of Texas, Houston, TX.

3. Pulmonology, Northwest Permanente, Hillsboro, OR.

4. Pulmonary & Critical Care, University of Virginia, Charlottesville, VA.

5. Critical Care Medicine, Hawaii Permanente Medical Group, Honolulu, HI.

Abstract

OBJECTIVES: To identify cytokine signature clusters in patients with septic shock. DESIGN: Prospective observational cohort study. SETTING: Single academic center in the United States. PATIENTS: Adult (≥ 18 yr old) patients admitted to the medical ICU with septic shock requiring vasoactive medication support. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: One hundred fourteen patients with septic shock completed cytokine measurement at time of enrollment (t1) and 24 hours later (t2). Unsupervised random forest analysis of the change in cytokines over time, defined as delta (t2–t1), identified three clusters with distinct cytokine profiles. Patients in cluster 1 had the lowest initial levels of circulating cytokines that decreased over time. Patients in cluster 2 and cluster 3 had higher initial levels that decreased over time in cluster 2 and increased in cluster 3. Patients in clusters 2 and 3 had higher mortality compared with cluster 1 (clusters 1–3: 11% vs 31%; odds ratio [OR], 3.56 [1.10–14.23] vs 54% OR, 9.23 [2.89–37.22]). Cluster 3 was independently associated with in-hospital mortality (hazard ratio, 5.24; p = 0.005) in multivariable analysis. There were no significant differences in initial clinical severity scoring or steroid use between the clusters. Analysis of either t1 or t2 cytokine measurements alone or in combination did not reveal clusters with clear clinical significance. CONCLUSIONS: Longitudinal measurement of cytokine profiles at initiation of vasoactive medications and 24 hours later revealed three distinct cytokine signature clusters that correlated with clinical outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Critical Care and Intensive Care Medicine

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