Stratification to predict the response to antioxidant
| Autor: | Cristiane, Ritter, Larissa, Constantino, Monique, Michels, Renata Casagrande, Gonçalves, Cassiana, Fraga, Danusa, Damásio, Felipe, Dal-Pizzol |
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| Rok vydání: | 2019 |
| Předmět: |
Adult
Male Interleukin-6 Sepse Mediadores da inflamação Inflammation mediators Antioxidantes Deferoxamine Middle Aged Prognosis Antioxidants Acetylcysteine Rats Interleucina-6 Treatment Outcome Models animal Sepsis Animals Humans Original Article Rats Wistar Aged Retrospective Studies Modelos animais Ratos |
| Zdroj: | Revista Brasileira de Terapia Intensiva |
| ISSN: | 1982-4335 |
| Popis: | Objective To examine the effectiveness of stratification to identify and target antioxidant therapy for animal models of lethal sepsis and in patients who develop sustained hypotension. Methods Rats were subjected to sepsis induced by cecal ligation and puncture. Animals were divided into two groups: those with high and low plasma levels of interleukin-6. Following stratification, N-acetylcysteine plus deferoxamine or saline was administered to animals starting 3 and 12 hours after surgery. N-Acetylcysteine plus deferoxamine or placebo was administered within 12 hours of meeting the inclusion criteria in hypotensive patients. Results N-Acetylcysteine plus deferoxamine increased survival in the cecal ligation and puncture model when administered 3 and 12 hours after sepsis induction. When dividing animals that received antioxidants using plasma interleukin-6 levels, the protective effect was observed only in those animals with high IL-6 levels. The antioxidant effect of N-acetylcysteine + deferoxamine was similar in the two groups, but a significant decrease in plasma interleukin-6 levels was observed in the high-interleukin-6-level group. Compared with patients treated with antioxidants in the low-interleukin-6 subgroup, those in the high-interleukin-6 subgroup had a lower incidence of acute kidney injury but were not different in terms of acute kidney injury severity or intensive care unit mortality. Conclusion Targeting antioxidant therapy to a high inflammatory phenotype would select a responsive population. |
| Databáze: | OpenAIRE |
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