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Leptin independently predicts development of sepsis and its outcome

Authors :
Sofie Jacobsson
Peter Larsson
Göran Johansson
Margareta Norberg
Göran Wadell
Göran Hallmans
Ola Winsö
Stefan Söderberg
Source :
Journal of Inflammation, Vol 14, Iss 1, Pp 1-10 (2017)
Publication Year :
2017
Publisher :
BMC, 2017.

Abstract

Abstract Background Sepsis is a life-threatening condition and obesity is related to the clinical outcome. The underlying reasons are incompletely understood, but the adipocyte derived hormones leptin and adiponectin may be involved. Methods Patients aged 18 years or more with documented first time sepsis events were included in a nested case-referent study if they had participated in previous health surveys. Two matched referents free of known sepsis were identified. Circulating levels of leptin and adiponectin were determined in stored plasma, and their impact on a future sepsis event and its outcome was evaluated. Results We identified 152 patients (62% women) with a sepsis event and a previous participation in a health survey. Eighty-three % had also blood samples from the acute event. Hyperleptinemia at health survey associated with a future sepsis event (OR 1.77, 95% CI 1.04–3.00) and with hospital death. After adjustment for BMI leptin remained associated with sepsis in men, but not in women. High levels in the acute phase associated with increased risk for in hospital death in women (OR 4.18, 95% CI 1.17–15.00), while being protective in men (OR 0.05, 95% CI 0.01–0.48). Furthermore, leptin increased more from baseline to the acute phase in men than in women. Adiponectin did not predict sepsis and did not relate to outcome. Conclusions Hyperleptinemia independently predicted the development of sepsis and an unfavourable outcome in men, and inertia in the acute response related to worse outcome.

Details

Language :
English
ISSN :
14769255
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Inflammation
Publication Type :
Academic Journal
Accession number :
edsdoj.7cfc199b4ae44aa6af80843957a58f41
Document Type :
article
Full Text :
https://doi.org/10.1186/s12950-017-0167-2