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Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients
Recent studies have shown that the cytochrome P450 (CYP) 3A phenotype marker 4β‐hydroxycholesterol/cholesterol (4βOHC/C) ratio is negatively correlated with body weight in healthy volunteers, and that obese patients have lower 4βOHC levels than healthy controls. However, 4βOHC/C ratio in underweight...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134200/ https://www.ncbi.nlm.nih.gov/pubmed/30214813 http://dx.doi.org/10.1002/prp2.430 |
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author | Hole, Kristine Heiberg, Petra L. Gjestad, Caroline Mehus, Lise L. Rø, Øyvind Molden, Espen |
author_facet | Hole, Kristine Heiberg, Petra L. Gjestad, Caroline Mehus, Lise L. Rø, Øyvind Molden, Espen |
author_sort | Hole, Kristine |
collection | PubMed |
description | Recent studies have shown that the cytochrome P450 (CYP) 3A phenotype marker 4β‐hydroxycholesterol/cholesterol (4βOHC/C) ratio is negatively correlated with body weight in healthy volunteers, and that obese patients have lower 4βOHC levels than healthy controls. However, 4βOHC/C ratio in underweight patients has yet to be reported. The aim of this study was to examine potential differences in CYP3A activity between underweight patients with anorexia nervosa and normal‐weight volunteers by measuring plasma 4βOHC/C ratio. Furthermore, we wished to describe any association between body mass index (BMI) and 4βOHC/C ratio in underweight patients. A total of 20 underweight patients and 16 normal‐weight volunteers were included in the study, all females. Underweight patients had a median 4βOHC/C ratio (molar ratio × 10(−5)) of 2.52 (range, 0.90–11.3) compared to 1.29 (0.56–2.09) in normal‐weight subjects (Mann‐Whitney P = 0.0005). 4βOHC/C ratio was negatively correlated with BMI in underweight patients (r = −0.56, P = 0.011), and in the whole study population (r = −0.67, P < 0.0001). This suggests that the negative correlation between 4βOHC/C and BMI, which has previously been reported between 4βOHC/C and body weight in healthy volunteers, extends to underweight patients. The findings indicate that CYP3A activity increases with decreasing BMI, resulting in higher CYP3A activity in underweight patients compared to normal‐weight subjects. The potential clinical relevance of this needs to be studied further by comparing pharmacokinetics of drugs subjected to CYP3A‐mediated metabolism in underweight vs. normal‐weight individuals. |
format | Online Article Text |
id | pubmed-6134200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61342002018-09-13 Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients Hole, Kristine Heiberg, Petra L. Gjestad, Caroline Mehus, Lise L. Rø, Øyvind Molden, Espen Pharmacol Res Perspect Original Articles Recent studies have shown that the cytochrome P450 (CYP) 3A phenotype marker 4β‐hydroxycholesterol/cholesterol (4βOHC/C) ratio is negatively correlated with body weight in healthy volunteers, and that obese patients have lower 4βOHC levels than healthy controls. However, 4βOHC/C ratio in underweight patients has yet to be reported. The aim of this study was to examine potential differences in CYP3A activity between underweight patients with anorexia nervosa and normal‐weight volunteers by measuring plasma 4βOHC/C ratio. Furthermore, we wished to describe any association between body mass index (BMI) and 4βOHC/C ratio in underweight patients. A total of 20 underweight patients and 16 normal‐weight volunteers were included in the study, all females. Underweight patients had a median 4βOHC/C ratio (molar ratio × 10(−5)) of 2.52 (range, 0.90–11.3) compared to 1.29 (0.56–2.09) in normal‐weight subjects (Mann‐Whitney P = 0.0005). 4βOHC/C ratio was negatively correlated with BMI in underweight patients (r = −0.56, P = 0.011), and in the whole study population (r = −0.67, P < 0.0001). This suggests that the negative correlation between 4βOHC/C and BMI, which has previously been reported between 4βOHC/C and body weight in healthy volunteers, extends to underweight patients. The findings indicate that CYP3A activity increases with decreasing BMI, resulting in higher CYP3A activity in underweight patients compared to normal‐weight subjects. The potential clinical relevance of this needs to be studied further by comparing pharmacokinetics of drugs subjected to CYP3A‐mediated metabolism in underweight vs. normal‐weight individuals. John Wiley and Sons Inc. 2018-09-11 /pmc/articles/PMC6134200/ /pubmed/30214813 http://dx.doi.org/10.1002/prp2.430 Text en © 2018 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hole, Kristine Heiberg, Petra L. Gjestad, Caroline Mehus, Lise L. Rø, Øyvind Molden, Espen Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title | Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title_full | Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title_fullStr | Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title_full_unstemmed | Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title_short | Elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
title_sort | elevated 4β‐hydroxycholesterol/cholesterol ratio in anorexia nervosa patients |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134200/ https://www.ncbi.nlm.nih.gov/pubmed/30214813 http://dx.doi.org/10.1002/prp2.430 |
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