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Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study

To evaluate whether parameters of obstructive sleep apnoea (OSA) associate with cholesterol metabolism before and after weight reduction, 42 middle-aged overweight subjects with mild OSA were randomised to intensive lifestyle intervention (N = 23) or to control group (N = 18) with routine lifestyle...

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Autores principales: Hallikainen, Maarit, Tuomilehto, Henri, Martikainen, Tarja, Vanninen, Esko, Seppä, Juha, Kokkarinen, Jouko, Randell, Jukka, Gylling, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671279/
https://www.ncbi.nlm.nih.gov/pubmed/23762545
http://dx.doi.org/10.1155/2013/769457
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author Hallikainen, Maarit
Tuomilehto, Henri
Martikainen, Tarja
Vanninen, Esko
Seppä, Juha
Kokkarinen, Jouko
Randell, Jukka
Gylling, Helena
author_facet Hallikainen, Maarit
Tuomilehto, Henri
Martikainen, Tarja
Vanninen, Esko
Seppä, Juha
Kokkarinen, Jouko
Randell, Jukka
Gylling, Helena
author_sort Hallikainen, Maarit
collection PubMed
description To evaluate whether parameters of obstructive sleep apnoea (OSA) associate with cholesterol metabolism before and after weight reduction, 42 middle-aged overweight subjects with mild OSA were randomised to intensive lifestyle intervention (N = 23) or to control group (N = 18) with routine lifestyle counselling only. Cholesterol metabolism was evaluated with serum noncholesterol sterol ratios to cholesterol, surrogate markers of cholesterol absorption (cholestanol and plant sterols) and synthesis (cholestenol, desmosterol, and lathosterol) at baseline and after 1-year intervention. At baseline, arterial oxygen saturation (Sa(O(2))) was associated with serum campesterol (P < 0.05) and inversely with desmosterol ratios (P < 0.001) independently of gender, BMI, and homeostasis model assessment index of insulin resistance (HOMA-IR). Apnoea-hypopnoea index (AHI) was not associated with cholesterol metabolism. Weight reduction significantly increased Sa(O(2))and serum cholestanol and decreased AHI and serum cholestenol ratios. In the groups combined, the changes in AHI were inversely associated with changes of cholestanol and positively with cholestenol ratios independent of gender and the changes of BMI and HOMA-IR (P < 0.05). In conclusion, mild OSA seemed to be associated with cholesterol metabolism independent of BMI and HOMA-IR. Weight reduction increased the markers of cholesterol absorption and decreased those of cholesterol synthesis in the overweight subjects with mild OSA.
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spelling pubmed-36712792013-06-12 Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study Hallikainen, Maarit Tuomilehto, Henri Martikainen, Tarja Vanninen, Esko Seppä, Juha Kokkarinen, Jouko Randell, Jukka Gylling, Helena Cholesterol Research Article To evaluate whether parameters of obstructive sleep apnoea (OSA) associate with cholesterol metabolism before and after weight reduction, 42 middle-aged overweight subjects with mild OSA were randomised to intensive lifestyle intervention (N = 23) or to control group (N = 18) with routine lifestyle counselling only. Cholesterol metabolism was evaluated with serum noncholesterol sterol ratios to cholesterol, surrogate markers of cholesterol absorption (cholestanol and plant sterols) and synthesis (cholestenol, desmosterol, and lathosterol) at baseline and after 1-year intervention. At baseline, arterial oxygen saturation (Sa(O(2))) was associated with serum campesterol (P < 0.05) and inversely with desmosterol ratios (P < 0.001) independently of gender, BMI, and homeostasis model assessment index of insulin resistance (HOMA-IR). Apnoea-hypopnoea index (AHI) was not associated with cholesterol metabolism. Weight reduction significantly increased Sa(O(2))and serum cholestanol and decreased AHI and serum cholestenol ratios. In the groups combined, the changes in AHI were inversely associated with changes of cholestanol and positively with cholestenol ratios independent of gender and the changes of BMI and HOMA-IR (P < 0.05). In conclusion, mild OSA seemed to be associated with cholesterol metabolism independent of BMI and HOMA-IR. Weight reduction increased the markers of cholesterol absorption and decreased those of cholesterol synthesis in the overweight subjects with mild OSA. Hindawi Publishing Corporation 2013 2013-05-16 /pmc/articles/PMC3671279/ /pubmed/23762545 http://dx.doi.org/10.1155/2013/769457 Text en Copyright © 2013 Maarit Hallikainen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hallikainen, Maarit
Tuomilehto, Henri
Martikainen, Tarja
Vanninen, Esko
Seppä, Juha
Kokkarinen, Jouko
Randell, Jukka
Gylling, Helena
Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title_full Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title_fullStr Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title_full_unstemmed Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title_short Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study
title_sort cholesterol metabolism and weight reduction in subjects with mild obstructive sleep apnoea: a randomised, controlled study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671279/
https://www.ncbi.nlm.nih.gov/pubmed/23762545
http://dx.doi.org/10.1155/2013/769457
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