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Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis

INTRODUCTION: Multiple sclerosis (MS) has been associated with both a poor vitamin D status and hyperactivity of the hypothalamus–pituitary–adrenal (HPA) axis. Since nuclear receptor ligands may regulate each other, we explored the association of vitamin D(3) supplements with circadian cortisol leve...

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Autores principales: Rolf, Linda, Damoiseaux, Jan, Huitinga, Inge, Kimenai, Dorien, van den Ouweland, Jody, Hupperts, Raymond, Smolders, Joost
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933207/
https://www.ncbi.nlm.nih.gov/pubmed/29755397
http://dx.doi.org/10.3389/fneur.2018.00263
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author Rolf, Linda
Damoiseaux, Jan
Huitinga, Inge
Kimenai, Dorien
van den Ouweland, Jody
Hupperts, Raymond
Smolders, Joost
author_facet Rolf, Linda
Damoiseaux, Jan
Huitinga, Inge
Kimenai, Dorien
van den Ouweland, Jody
Hupperts, Raymond
Smolders, Joost
author_sort Rolf, Linda
collection PubMed
description INTRODUCTION: Multiple sclerosis (MS) has been associated with both a poor vitamin D status and hyperactivity of the hypothalamus–pituitary–adrenal (HPA) axis. Since nuclear receptor ligands may regulate each other, we explored the association of vitamin D(3) supplements with circadian cortisol levels in a double-blind and placebo-controlled supplementation study. METHODS: Female patients with relapsing-remitting MS received vitamin D(3) supplements (4,000 IU/day; n = 22) or placebo (n = 19) during 16 weeks. Salivary cortisol levels, repeatedly measured during the day, and serum 25(OH)D levels were assessed before (T0) and after (T1) this treatment period. RESULTS: Median 25(OH)D levels at T1 were 139.9 (interquartile range 123.5–161.2) and 74.5 nmol/L (58.6–88.1) in the vitamin D(3) and placebo group, respectively (p < 0.001). Comparisons within and between groups showed no differences in area under the curve (AUC) and slope of the cortisol day curve. Although the AUC of the cortisol awakening response (CAR, sampling each 15 min the first hour after awakening) showed a reduction over time in the vitamin D(3) group [39.16 nmol/L (27.41–42.07) at T0 to 33.37 nmol/L (26.75–38.08) at T1] compared to the placebo group [33.90 nmol/L (25.92–44.61) at T0 to 35.00 nmol/L (25.46–49.23) at T1; p = 0.044], there was no significant difference in AUC of CAR at T1 corrected for baseline AUC of CAR (p = 0.066). CONCLUSION: Suppression of HPA-axis activity by vitamin D(3) supplements in non-depressed MS patients may be best reflected by CAR as primary outcome measure. Further studies should address this interaction and its potential implications for the disease course of MS. REGISTRATION: This study was registered on ClinicalTrials.gov (NCT02096133) and EudraCT (2014-000728-97).
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spelling pubmed-59332072018-05-11 Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis Rolf, Linda Damoiseaux, Jan Huitinga, Inge Kimenai, Dorien van den Ouweland, Jody Hupperts, Raymond Smolders, Joost Front Neurol Neuroscience INTRODUCTION: Multiple sclerosis (MS) has been associated with both a poor vitamin D status and hyperactivity of the hypothalamus–pituitary–adrenal (HPA) axis. Since nuclear receptor ligands may regulate each other, we explored the association of vitamin D(3) supplements with circadian cortisol levels in a double-blind and placebo-controlled supplementation study. METHODS: Female patients with relapsing-remitting MS received vitamin D(3) supplements (4,000 IU/day; n = 22) or placebo (n = 19) during 16 weeks. Salivary cortisol levels, repeatedly measured during the day, and serum 25(OH)D levels were assessed before (T0) and after (T1) this treatment period. RESULTS: Median 25(OH)D levels at T1 were 139.9 (interquartile range 123.5–161.2) and 74.5 nmol/L (58.6–88.1) in the vitamin D(3) and placebo group, respectively (p < 0.001). Comparisons within and between groups showed no differences in area under the curve (AUC) and slope of the cortisol day curve. Although the AUC of the cortisol awakening response (CAR, sampling each 15 min the first hour after awakening) showed a reduction over time in the vitamin D(3) group [39.16 nmol/L (27.41–42.07) at T0 to 33.37 nmol/L (26.75–38.08) at T1] compared to the placebo group [33.90 nmol/L (25.92–44.61) at T0 to 35.00 nmol/L (25.46–49.23) at T1; p = 0.044], there was no significant difference in AUC of CAR at T1 corrected for baseline AUC of CAR (p = 0.066). CONCLUSION: Suppression of HPA-axis activity by vitamin D(3) supplements in non-depressed MS patients may be best reflected by CAR as primary outcome measure. Further studies should address this interaction and its potential implications for the disease course of MS. REGISTRATION: This study was registered on ClinicalTrials.gov (NCT02096133) and EudraCT (2014-000728-97). Frontiers Media S.A. 2018-04-26 /pmc/articles/PMC5933207/ /pubmed/29755397 http://dx.doi.org/10.3389/fneur.2018.00263 Text en Copyright © 2018 Rolf, Damoiseaux, Huitinga, Kimenai, van den Ouweland, Hupperts and Smolders. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Rolf, Linda
Damoiseaux, Jan
Huitinga, Inge
Kimenai, Dorien
van den Ouweland, Jody
Hupperts, Raymond
Smolders, Joost
Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title_full Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title_fullStr Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title_full_unstemmed Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title_short Stress-Axis Regulation by Vitamin D(3) in Multiple Sclerosis
title_sort stress-axis regulation by vitamin d(3) in multiple sclerosis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933207/
https://www.ncbi.nlm.nih.gov/pubmed/29755397
http://dx.doi.org/10.3389/fneur.2018.00263
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