<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>37(2)</volume><submitter>Ma Y</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Previous studies found that vitamin D receptor (VDR) TaqI, BsmI, FokI and ApaI gene polymorphisms are associated with several inflammatory diseases. However, the relationship between VDR gene polymorphisms and chronic spontaneous urticaria (CSU) is not clear.&lt;h4>Aim&lt;/h4>The purpose of our study was to explore the relationship between the polymorphism of VDR and the incidence of chronic spontaneous urticaria in the Chinese Han population. Meanwhile, the vitamin D levels in patients with chronic spontaneous urticaria were also detected and the effects of VDR gene polymorphism on vitamin D levels were detected.&lt;h4>Material and methods&lt;/h4>The genotypes of four VDR polymorphisms (TaqI, BsmI, ApaI, and FokI) were studied using allele-specific PCR analysis in 90 CSU patients and 90 healthy controls.&lt;h4>Results&lt;/h4>Compared to the control group, the mutant allele (C) of FokI were more common in patients with CSU (57.2% vs. 45%, &lt;i>p&lt;/i> = 0.020, odds ratio (OR) = 0.612, 95% confidence interval (CI): 0.403-0.928). We found that serum vitamin D levels were significantly lower in CSU patients than in healthy controls (&lt;i>p&lt;/i> = 0.023). However, the effect of VDR gene polymorphism on vitamin D levels was not found in patients of CSU.&lt;h4>Conclusions&lt;/h4>We first reported the effect of VDR gene FokI (rs2228570) polymorphism on the incidence of chronic spontaneous urticaria in the Chinese Han population.</pubmed_abstract><journal>Postepy dermatologii i alergologii</journal><pagination>250-254</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7262806</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Associations between vitamin D receptor gene polymorphisms and chronic spontaneous urticaria in Chinese Han population.</pubmed_title><pmcid>PMC7262806</pmcid><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Cui P</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Xiang Z</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Yao X</pubmed_authors><pubmed_authors>Feng S</pubmed_authors><pubmed_authors>Lin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Associations between vitamin D receptor gene polymorphisms and chronic spontaneous urticaria in Chinese Han population.</name><description>&lt;h4>Introduction&lt;/h4>Previous studies found that vitamin D receptor (VDR) TaqI, BsmI, FokI and ApaI gene polymorphisms are associated with several inflammatory diseases. However, the relationship between VDR gene polymorphisms and chronic spontaneous urticaria (CSU) is not clear.&lt;h4>Aim&lt;/h4>The purpose of our study was to explore the relationship between the polymorphism of VDR and the incidence of chronic spontaneous urticaria in the Chinese Han population. Meanwhile, the vitamin D levels in patients with chronic spontaneous urticaria were also detected and the effects of VDR gene polymorphism on vitamin D levels were detected.&lt;h4>Material and methods&lt;/h4>The genotypes of four VDR polymorphisms (TaqI, BsmI, ApaI, and FokI) were studied using allele-specific PCR analysis in 90 CSU patients and 90 healthy controls.&lt;h4>Results&lt;/h4>Compared to the control group, the mutant allele (C) of FokI were more common in patients with CSU (57.2% vs. 45%, &lt;i>p&lt;/i> = 0.020, odds ratio (OR) = 0.612, 95% confidence interval (CI): 0.403-0.928). We found that serum vitamin D levels were significantly lower in CSU patients than in healthy controls (&lt;i>p&lt;/i> = 0.023). However, the effect of VDR gene polymorphism on vitamin D levels was not found in patients of CSU.&lt;h4>Conclusions&lt;/h4>We first reported the effect of VDR gene FokI (rs2228570) polymorphism on the incidence of chronic spontaneous urticaria in the Chinese Han population.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2024-02-15T13:25:08.425Z</modification><creation>2020-06-05T07:08:21Z</creation></dates><accession>S-EPMC7262806</accession><cross_references><pubmed>32489362</pubmed><doi>10.5114/ada.2020.94843</doi></cross_references></HashMap>