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Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome
BACKGROUND: Recent studies suggest that adipose tissue hormones are involved in the pathogenesis of obstructive sleep apnoea syndrome (OSAS). The role of leptin, obestatin and apelin still needs to be established. MATERIAL/METHODS: Ten patients with newly diagnosed OSAS (AHI >10/h and ESS >10...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524733/ https://www.ncbi.nlm.nih.gov/pubmed/21358603 http://dx.doi.org/10.12659/MSM.881450 |
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author | Zirlik, Sabine Hauck, Tabea Fuchs, Florian Siegfried Neurath, Markus Friedrich Konturek, Peter Christopher Harsch, Igor Alexander |
author_facet | Zirlik, Sabine Hauck, Tabea Fuchs, Florian Siegfried Neurath, Markus Friedrich Konturek, Peter Christopher Harsch, Igor Alexander |
author_sort | Zirlik, Sabine |
collection | PubMed |
description | BACKGROUND: Recent studies suggest that adipose tissue hormones are involved in the pathogenesis of obstructive sleep apnoea syndrome (OSAS). The role of leptin, obestatin and apelin still needs to be established. MATERIAL/METHODS: Ten patients with newly diagnosed OSAS (AHI >10/h and ESS >10 points) were enrolled in the study as well as ten healthy volunteers as controls. All underwent measurements for Leptin, Obestatin and Apelin in four hour intervals during diagnostic polysomnography for 24 h and the patients also three months after onset of CPAP treatment. Furthermore the HOMA-index and body composition were quantified. RESULTS: Plasma apelin levels in the patients decreased under CPAP therapy, but showed no significant difference in patients and volunteers. We found a positive correlation to AHI, BMI in the therapy group at all observation points. Leptin plasma levels were higher in the patient group and decreased after onset of CPAP therapy. Leptin plasma levels were positively correlated to the BMI, min. 02 and AHI in the patient group before therapy. Plasma obestatin levels did not differ significantly in these three observation groups, but were partly correlated to AHI and weight in the newly diagnosed OSAS group. CONCLUSIONS: In agreement with previous investigations, we could demonstrate a difference in leptin plasma levels between healthy volunteers and patients with newly diagnosed OSAS. Apelin decreases under CPAP therapy, but not significantly. Obestatin remains unchanged after onset of CPAP. We further found a linkage between leptin plasma levels and BMI, AHI and weight in the untreated patient group. |
format | Online Article Text |
id | pubmed-3524733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35247332013-04-24 Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome Zirlik, Sabine Hauck, Tabea Fuchs, Florian Siegfried Neurath, Markus Friedrich Konturek, Peter Christopher Harsch, Igor Alexander Med Sci Monit Clinical Research BACKGROUND: Recent studies suggest that adipose tissue hormones are involved in the pathogenesis of obstructive sleep apnoea syndrome (OSAS). The role of leptin, obestatin and apelin still needs to be established. MATERIAL/METHODS: Ten patients with newly diagnosed OSAS (AHI >10/h and ESS >10 points) were enrolled in the study as well as ten healthy volunteers as controls. All underwent measurements for Leptin, Obestatin and Apelin in four hour intervals during diagnostic polysomnography for 24 h and the patients also three months after onset of CPAP treatment. Furthermore the HOMA-index and body composition were quantified. RESULTS: Plasma apelin levels in the patients decreased under CPAP therapy, but showed no significant difference in patients and volunteers. We found a positive correlation to AHI, BMI in the therapy group at all observation points. Leptin plasma levels were higher in the patient group and decreased after onset of CPAP therapy. Leptin plasma levels were positively correlated to the BMI, min. 02 and AHI in the patient group before therapy. Plasma obestatin levels did not differ significantly in these three observation groups, but were partly correlated to AHI and weight in the newly diagnosed OSAS group. CONCLUSIONS: In agreement with previous investigations, we could demonstrate a difference in leptin plasma levels between healthy volunteers and patients with newly diagnosed OSAS. Apelin decreases under CPAP therapy, but not significantly. Obestatin remains unchanged after onset of CPAP. We further found a linkage between leptin plasma levels and BMI, AHI and weight in the untreated patient group. International Scientific Literature, Inc. 2011-03-01 /pmc/articles/PMC3524733/ /pubmed/21358603 http://dx.doi.org/10.12659/MSM.881450 Text en © Med Sci Monit, 2011 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. |
spellingShingle | Clinical Research Zirlik, Sabine Hauck, Tabea Fuchs, Florian Siegfried Neurath, Markus Friedrich Konturek, Peter Christopher Harsch, Igor Alexander Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title | Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title_full | Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title_fullStr | Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title_full_unstemmed | Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title_short | Leptin, Obestatin and Apelin levels in patients with obstructive sleep apnoea syndrome |
title_sort | leptin, obestatin and apelin levels in patients with obstructive sleep apnoea syndrome |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524733/ https://www.ncbi.nlm.nih.gov/pubmed/21358603 http://dx.doi.org/10.12659/MSM.881450 |
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