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Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients
INTRODUCTION: Although psoriasis and obstructive sleep apnea syndrome (OSAS) are associated with systemic inflammation, studies on their potential bilateral relationship are not sufficient. AIM: To investigate vitamin D levels and receptor gene polymorphisms in patients with OSAS and psoriasis and t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131946/ https://www.ncbi.nlm.nih.gov/pubmed/35645681 http://dx.doi.org/10.5114/ada.2021.106031 |
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author | Albayrak, Hülya Fazlıoğlu, Nevin Batar, Bahadır Yanık, Mehmet Emin Oran, Mustafa Altıntaş, Nejat |
author_facet | Albayrak, Hülya Fazlıoğlu, Nevin Batar, Bahadır Yanık, Mehmet Emin Oran, Mustafa Altıntaş, Nejat |
author_sort | Albayrak, Hülya |
collection | PubMed |
description | INTRODUCTION: Although psoriasis and obstructive sleep apnea syndrome (OSAS) are associated with systemic inflammation, studies on their potential bilateral relationship are not sufficient. AIM: To investigate vitamin D levels and receptor gene polymorphisms in patients with OSAS and psoriasis and the associations with these diseases. MATERIAL AND METHODS: One hundred thirty-seven patients included in the study consisted of 4 different groups: group 1, those with both diseases; group 2, those with OSAS only; group 3, patients with psoriasis only; and group 4, healthy controls. The patients’ serum calcium, phosphorus, AHI, Epworth Sleepiness Scale, Psoriasis Area Severity Index, and VDR TagI, ApaI, BsmI polymorphisms were compared. RESULTS: Vitamin D levels of groups 1, 2 and 3 were found to be lower than in controls. There was no statistically significant correlation between VDR TagI, ApaI, BsmI gene polymorphisms of the groups. Vitamin D levels were significantly higher in patients with heterozygous ApaI genotype (A/C) compared to patients with normal (A/A) or homozygous mutant (C/C) genotype (p < 0.05). No relationship was determined between VDR TagI, ApaI, BsmI, and the other parameters. CONCLUSIONS: In our study, 1,25(OH)(2)-vitamin D(3) levels were significantly lower in all disease groups compared to the control group. Although there is no difference between the groups in terms of VDR gene polymorphism, we think that there may be a bidirectional relationship between these diseases based on the low vitamin D levels. |
format | Online Article Text |
id | pubmed-9131946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-91319462022-05-26 Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients Albayrak, Hülya Fazlıoğlu, Nevin Batar, Bahadır Yanık, Mehmet Emin Oran, Mustafa Altıntaş, Nejat Postepy Dermatol Alergol Original Paper INTRODUCTION: Although psoriasis and obstructive sleep apnea syndrome (OSAS) are associated with systemic inflammation, studies on their potential bilateral relationship are not sufficient. AIM: To investigate vitamin D levels and receptor gene polymorphisms in patients with OSAS and psoriasis and the associations with these diseases. MATERIAL AND METHODS: One hundred thirty-seven patients included in the study consisted of 4 different groups: group 1, those with both diseases; group 2, those with OSAS only; group 3, patients with psoriasis only; and group 4, healthy controls. The patients’ serum calcium, phosphorus, AHI, Epworth Sleepiness Scale, Psoriasis Area Severity Index, and VDR TagI, ApaI, BsmI polymorphisms were compared. RESULTS: Vitamin D levels of groups 1, 2 and 3 were found to be lower than in controls. There was no statistically significant correlation between VDR TagI, ApaI, BsmI gene polymorphisms of the groups. Vitamin D levels were significantly higher in patients with heterozygous ApaI genotype (A/C) compared to patients with normal (A/A) or homozygous mutant (C/C) genotype (p < 0.05). No relationship was determined between VDR TagI, ApaI, BsmI, and the other parameters. CONCLUSIONS: In our study, 1,25(OH)(2)-vitamin D(3) levels were significantly lower in all disease groups compared to the control group. Although there is no difference between the groups in terms of VDR gene polymorphism, we think that there may be a bidirectional relationship between these diseases based on the low vitamin D levels. Termedia Publishing House 2021-10-25 2022-04 /pmc/articles/PMC9131946/ /pubmed/35645681 http://dx.doi.org/10.5114/ada.2021.106031 Text en Copyright: © 2022 Termedia Sp. z o. o. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Albayrak, Hülya Fazlıoğlu, Nevin Batar, Bahadır Yanık, Mehmet Emin Oran, Mustafa Altıntaş, Nejat Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title | Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title_full | Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title_fullStr | Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title_full_unstemmed | Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title_short | Relationship between vitamin D in obstructive sleep apnea syndrome and psoriasis patients |
title_sort | relationship between vitamin d in obstructive sleep apnea syndrome and psoriasis patients |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131946/ https://www.ncbi.nlm.nih.gov/pubmed/35645681 http://dx.doi.org/10.5114/ada.2021.106031 |
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