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Leptin levels after subarachnoid haemorrhage are gender dependent
BACKGROUND: Subarachnoid hemorrhage (SAH) is a neurological disease where the majority of the patients are critically ill. The adipokine leptin has in cerebral emergencies been related to severity of disease and to adverse outcome. The aim of this study was to examine leptin levels over time after S...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899384/ https://www.ncbi.nlm.nih.gov/pubmed/27350906 http://dx.doi.org/10.1186/s40064-016-2321-3 |
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author | Lindgren, Cecilia Naredi, Silvana Söderberg, Stefan Koskinen, Lars-Owe Hultin, Magnus |
author_facet | Lindgren, Cecilia Naredi, Silvana Söderberg, Stefan Koskinen, Lars-Owe Hultin, Magnus |
author_sort | Lindgren, Cecilia |
collection | PubMed |
description | BACKGROUND: Subarachnoid hemorrhage (SAH) is a neurological disease where the majority of the patients are critically ill. The adipokine leptin has in cerebral emergencies been related to severity of disease and to adverse outcome. The aim of this study was to examine leptin levels over time after SAH and associations to gender, age, body mass index, severity of disease, parenteral lipids, systemic organ failure and outcome. METHODS: Prospective observational study in 56 patients. Leptin was obtained 0–240 h after SAH, in 48 h intervals. Severity of disease was assessed with the Hunt and Hess score, organ failure with the sequential organ failure assessment score, and outcome with Glasgow outcome scale. Leptin levels in the SAH group were compared with controls from the same geographical area. RESULTS: At admission, Leptin was significantly higher in SAH patients compared to controls, both in female (28.6 ± 25.6 vs 13.0 ± 2.3 ng/mL, p = 0.001) and male patients (13.3 ± 8.4 vs 4.3 ± 0.7 ng/mL, p = 0.001). Leptin levels remained stable over time. Female patients had significantly higher leptin levels than male patients, and deceased female patients had higher leptin levels than female survivors (85.5 ± 20.5 vs 50.5 ± 34.6, n = 4/35, p < 0.05). Leptin levels did not differ between male survivors and non-survivors. Leptin levels were not associated with severity of disease, organ failure or parenteral lipids. CONCLUSION: Leptin levels were significantly higher in both male and female patients compared to controls. Higher leptin levels were related to outcome and organ failure in women but not in men. When analysing leptin levels gender-related differences should be considered. |
format | Online Article Text |
id | pubmed-4899384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-48993842016-06-27 Leptin levels after subarachnoid haemorrhage are gender dependent Lindgren, Cecilia Naredi, Silvana Söderberg, Stefan Koskinen, Lars-Owe Hultin, Magnus Springerplus Research BACKGROUND: Subarachnoid hemorrhage (SAH) is a neurological disease where the majority of the patients are critically ill. The adipokine leptin has in cerebral emergencies been related to severity of disease and to adverse outcome. The aim of this study was to examine leptin levels over time after SAH and associations to gender, age, body mass index, severity of disease, parenteral lipids, systemic organ failure and outcome. METHODS: Prospective observational study in 56 patients. Leptin was obtained 0–240 h after SAH, in 48 h intervals. Severity of disease was assessed with the Hunt and Hess score, organ failure with the sequential organ failure assessment score, and outcome with Glasgow outcome scale. Leptin levels in the SAH group were compared with controls from the same geographical area. RESULTS: At admission, Leptin was significantly higher in SAH patients compared to controls, both in female (28.6 ± 25.6 vs 13.0 ± 2.3 ng/mL, p = 0.001) and male patients (13.3 ± 8.4 vs 4.3 ± 0.7 ng/mL, p = 0.001). Leptin levels remained stable over time. Female patients had significantly higher leptin levels than male patients, and deceased female patients had higher leptin levels than female survivors (85.5 ± 20.5 vs 50.5 ± 34.6, n = 4/35, p < 0.05). Leptin levels did not differ between male survivors and non-survivors. Leptin levels were not associated with severity of disease, organ failure or parenteral lipids. CONCLUSION: Leptin levels were significantly higher in both male and female patients compared to controls. Higher leptin levels were related to outcome and organ failure in women but not in men. When analysing leptin levels gender-related differences should be considered. Springer International Publishing 2016-05-27 /pmc/articles/PMC4899384/ /pubmed/27350906 http://dx.doi.org/10.1186/s40064-016-2321-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Lindgren, Cecilia Naredi, Silvana Söderberg, Stefan Koskinen, Lars-Owe Hultin, Magnus Leptin levels after subarachnoid haemorrhage are gender dependent |
title | Leptin levels after subarachnoid haemorrhage are gender dependent |
title_full | Leptin levels after subarachnoid haemorrhage are gender dependent |
title_fullStr | Leptin levels after subarachnoid haemorrhage are gender dependent |
title_full_unstemmed | Leptin levels after subarachnoid haemorrhage are gender dependent |
title_short | Leptin levels after subarachnoid haemorrhage are gender dependent |
title_sort | leptin levels after subarachnoid haemorrhage are gender dependent |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899384/ https://www.ncbi.nlm.nih.gov/pubmed/27350906 http://dx.doi.org/10.1186/s40064-016-2321-3 |
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