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Low Vitamin D in Narcolepsy with Cataplexy

BACKGROUND: Narcolepsy with cataplexy (NC) is currently thought to be an autoimmune-mediated disorder in which environmental risk factors make a significant contribution to its development. It was proposed that vitamin D deficiency plays a role in autoimmune diseases. Here we investigated whether NC...

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Autores principales: Carlander, Bertrand, Puech-Cathala, Anne Marie, Jaussent, Isabelle, Scholz, Sabine, Bayard, Sophie, Cochen, Valérie, Dauvilliers, Yves
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102118/
https://www.ncbi.nlm.nih.gov/pubmed/21633708
http://dx.doi.org/10.1371/journal.pone.0020433
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author Carlander, Bertrand
Puech-Cathala, Anne Marie
Jaussent, Isabelle
Scholz, Sabine
Bayard, Sophie
Cochen, Valérie
Dauvilliers, Yves
author_facet Carlander, Bertrand
Puech-Cathala, Anne Marie
Jaussent, Isabelle
Scholz, Sabine
Bayard, Sophie
Cochen, Valérie
Dauvilliers, Yves
author_sort Carlander, Bertrand
collection PubMed
description BACKGROUND: Narcolepsy with cataplexy (NC) is currently thought to be an autoimmune-mediated disorder in which environmental risk factors make a significant contribution to its development. It was proposed that vitamin D deficiency plays a role in autoimmune diseases. Here we investigated whether NC can be associated with 25-hydroxyvitamin D (25(OH)D) level deficiency in patients with NC compared with gender- and age-matched normal controls. METHODOLOGY: Serum level of 25 (OH)D was determined in 51 European patients with typical NC compared to 55 age-, gender-, and ethnicity-matched healthy controls. Demographic and clinical data (age at onset, duration and severity of disease at baseline, and treatment intake at time of study) and season of blood sampling were collected to control for confounding variables. PRINCIPAL FINDINGS: Serum 25(OH)D concentration was lower in NC compared to controls (median, 59.45 nmol/l [extreme values 24.05–124.03] vs. 74.73 nmol/l [26.88–167.48] p = 0.0039). Patients with NC had significantly greater vitamin D deficiency (<75 nmol/l) than controls (72.5% vs 50.9%, p = 0.0238). Division into quartiles of the whole sample revealed that the risk of being affected with NC increased with lower 25(OH)D level, with a 5.34 OR [1.65–17.27] for the lowest quartile (p = 0.0051). Further adjustment for BMI did not modify the strength of the association (OR: 3.63, 95% CI = 1.06–12.46, p = 0.0191). No between BMI and 25(OH)D interaction, and no correlation between 25(OH)D level and disease duration or severity or treatment intake were found in NC. CONCLUSION: We found a higher frequency of vitamin D deficiency in NC. Further studies are needed to assess the contribution of hypovitaminosis D to the risk of developing narcolepsy, and to focus on the utility of assessing vitamin D status to correct potential deficiency.
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spelling pubmed-31021182011-06-01 Low Vitamin D in Narcolepsy with Cataplexy Carlander, Bertrand Puech-Cathala, Anne Marie Jaussent, Isabelle Scholz, Sabine Bayard, Sophie Cochen, Valérie Dauvilliers, Yves PLoS One Research Article BACKGROUND: Narcolepsy with cataplexy (NC) is currently thought to be an autoimmune-mediated disorder in which environmental risk factors make a significant contribution to its development. It was proposed that vitamin D deficiency plays a role in autoimmune diseases. Here we investigated whether NC can be associated with 25-hydroxyvitamin D (25(OH)D) level deficiency in patients with NC compared with gender- and age-matched normal controls. METHODOLOGY: Serum level of 25 (OH)D was determined in 51 European patients with typical NC compared to 55 age-, gender-, and ethnicity-matched healthy controls. Demographic and clinical data (age at onset, duration and severity of disease at baseline, and treatment intake at time of study) and season of blood sampling were collected to control for confounding variables. PRINCIPAL FINDINGS: Serum 25(OH)D concentration was lower in NC compared to controls (median, 59.45 nmol/l [extreme values 24.05–124.03] vs. 74.73 nmol/l [26.88–167.48] p = 0.0039). Patients with NC had significantly greater vitamin D deficiency (<75 nmol/l) than controls (72.5% vs 50.9%, p = 0.0238). Division into quartiles of the whole sample revealed that the risk of being affected with NC increased with lower 25(OH)D level, with a 5.34 OR [1.65–17.27] for the lowest quartile (p = 0.0051). Further adjustment for BMI did not modify the strength of the association (OR: 3.63, 95% CI = 1.06–12.46, p = 0.0191). No between BMI and 25(OH)D interaction, and no correlation between 25(OH)D level and disease duration or severity or treatment intake were found in NC. CONCLUSION: We found a higher frequency of vitamin D deficiency in NC. Further studies are needed to assess the contribution of hypovitaminosis D to the risk of developing narcolepsy, and to focus on the utility of assessing vitamin D status to correct potential deficiency. Public Library of Science 2011-05-25 /pmc/articles/PMC3102118/ /pubmed/21633708 http://dx.doi.org/10.1371/journal.pone.0020433 Text en Carlander et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Carlander, Bertrand
Puech-Cathala, Anne Marie
Jaussent, Isabelle
Scholz, Sabine
Bayard, Sophie
Cochen, Valérie
Dauvilliers, Yves
Low Vitamin D in Narcolepsy with Cataplexy
title Low Vitamin D in Narcolepsy with Cataplexy
title_full Low Vitamin D in Narcolepsy with Cataplexy
title_fullStr Low Vitamin D in Narcolepsy with Cataplexy
title_full_unstemmed Low Vitamin D in Narcolepsy with Cataplexy
title_short Low Vitamin D in Narcolepsy with Cataplexy
title_sort low vitamin d in narcolepsy with cataplexy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102118/
https://www.ncbi.nlm.nih.gov/pubmed/21633708
http://dx.doi.org/10.1371/journal.pone.0020433
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