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Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study
To evaluate the effects of 25-hydroxyvitamin D(3) (25OHD) on symptoms at the onset of the upper respiratory tract infection (URTI) in subjects with insufficient or deficient serum 25-hydroxyvitamin D levels, we conducted a post hoc analysis of data from a randomized, placebo-controlled study; the su...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764240/ https://www.ncbi.nlm.nih.gov/pubmed/33302570 http://dx.doi.org/10.3390/nu12123769 |
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author | Shimizu, Yoshiki Ito, Yukihiko Uotsu, Nobuo Yui, Kei |
author_facet | Shimizu, Yoshiki Ito, Yukihiko Uotsu, Nobuo Yui, Kei |
author_sort | Shimizu, Yoshiki |
collection | PubMed |
description | To evaluate the effects of 25-hydroxyvitamin D(3) (25OHD) on symptoms at the onset of the upper respiratory tract infection (URTI) in subjects with insufficient or deficient serum 25-hydroxyvitamin D levels, we conducted a post hoc analysis of data from a randomized, placebo-controlled study; the subjects received 10 μg of 25OHD per day or a placebo for 16 weeks. The Wisconsin Upper Respiratory Symptom Survey-21 was used to determine URTI. The study endpoints included WURSS-21 scores, number of URTI events, and proportion of medication (antibiotics, antipyretic analgesics) usage. We found that the physical symptom scores for “Runny nose,” “Sneezing,” and “Head congestion” were significantly lower in the 25OHD group than in the placebo group; for all items except “Breathe easily, “the quality of life” scores were significantly improved in the 25OHD group. There was no significant difference in the number of URTI events or the proportion of medication use between the groups. Collectively, the findings of this study indicate that a sufficient 25OHD intake can reduce physical symptoms at the onset of upper respiratory tract infection, particularly nasal symptoms, and may improve the quality of life at the time of onset. |
format | Online Article Text |
id | pubmed-7764240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77642402020-12-27 Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study Shimizu, Yoshiki Ito, Yukihiko Uotsu, Nobuo Yui, Kei Nutrients Article To evaluate the effects of 25-hydroxyvitamin D(3) (25OHD) on symptoms at the onset of the upper respiratory tract infection (URTI) in subjects with insufficient or deficient serum 25-hydroxyvitamin D levels, we conducted a post hoc analysis of data from a randomized, placebo-controlled study; the subjects received 10 μg of 25OHD per day or a placebo for 16 weeks. The Wisconsin Upper Respiratory Symptom Survey-21 was used to determine URTI. The study endpoints included WURSS-21 scores, number of URTI events, and proportion of medication (antibiotics, antipyretic analgesics) usage. We found that the physical symptom scores for “Runny nose,” “Sneezing,” and “Head congestion” were significantly lower in the 25OHD group than in the placebo group; for all items except “Breathe easily, “the quality of life” scores were significantly improved in the 25OHD group. There was no significant difference in the number of URTI events or the proportion of medication use between the groups. Collectively, the findings of this study indicate that a sufficient 25OHD intake can reduce physical symptoms at the onset of upper respiratory tract infection, particularly nasal symptoms, and may improve the quality of life at the time of onset. MDPI 2020-12-08 /pmc/articles/PMC7764240/ /pubmed/33302570 http://dx.doi.org/10.3390/nu12123769 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shimizu, Yoshiki Ito, Yukihiko Uotsu, Nobuo Yui, Kei Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title | Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title_full | Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title_fullStr | Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title_full_unstemmed | Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title_short | Intake of 25-Hydroxyvitamin D(3) May Reduce the Severity of Upper Respiratory Tract Infection: Post hoc Analysis of a Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study |
title_sort | intake of 25-hydroxyvitamin d(3) may reduce the severity of upper respiratory tract infection: post hoc analysis of a randomized, double-blind, placebo-controlled, parallel group comparison study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764240/ https://www.ncbi.nlm.nih.gov/pubmed/33302570 http://dx.doi.org/10.3390/nu12123769 |
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