Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28698
Title: Gene Expression Scoring of Immune Activity Levels for Precision Use of Hydrocortisone In Vasodilatory Shock.
Austin Authors: Yao, Lijing;Rey, Diego Ariel;Bulgarelli, Lucas;Kast, Rachel;Osborn, Jeff;Van Ark, Emily;Fang, Li Tai;Lau, Bayo;Lam, Hugo;Teixeira, Leonardo Maestri;Neto, Ary Serpa;Bellomo, Rinaldo ;Deliberato, Rodrigo Octávio
Affiliation: Intensive Care..
Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Australia..
Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia..
Department of Clinical Data Science, Endpoint Health Inc, Palo Alto, California, USA Bioinformatics Department, HypaHub Inc, San Jose, California, USA Department of Critical Care Medicine, Hospital Israelita Albert Einstein, São Paulo, Brazil..
Data Analytics Research and Evaluation (DARE) Centre..
Department of Critical Care, Melbourne Medical School, University of Melbourne, Austin Hospital, Melbourne, Australia..
Issue Date: 1-Mar-2022
Date: 2022
Publication information: Shock 2022; 57(3): 384-391
Abstract: Among patients with vasodilatory shock, gene expression scores may identify different immune states. We aimed to test whether such scores are robust in identifying patients' immune state and predicting response to hydrocortisone treatment in vasodilatory shock. We selected genes to generate continuous scores to define previously established subclasses of sepsis. We used these scores to identify a patient's immune state. We evaluated the potential for these states to assess the differential effect of hydrocortisone in two randomized clinical trials of hydrocortisone vs. placebo in vasodilatory shock. We initially identified genes associated with immune-adaptive, immune-innate, immune-coagulant functions. From these genes, 15 were most relevant to generate expression scores related to each of the functions. These scores were used to identify patients as immune-adaptive prevalent (IA-P) and immune-innate prevalent (IN-P). In IA-P patients, hydrocortisone therapy increased 28-day mortality in both trials (43.3% vs 14.7%, p = 0.028) and (57.1% vs 0.0%, p = 0.99). In IN-P patients, this effect was numerically reversed. Gene expression scores identified the immune state of vasodilatory shock patients, one of which (IA-P) identified those who may be harmed by hydrocortisone. Gene expression scores may help advance the field of personalized medicine.
URI: https://ahro.austin.org.au/austinjspui/handle/1/28698
DOI: 10.1097/SHK.0000000000001910
ORCID: 0000-0003-1520-9387
0000-0002-1650-8939
Journal: Shock (Augusta, Ga.)
PubMed URL: 35081076
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/35081076/
Type: Journal Article
Appears in Collections:Journal articles

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