<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>46</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>12(2)</volume><submitter>Awasthi N</submitter><pubmed_abstract>Asthma is a complex genetic disease. Vitamin D and vitamin D receptor (&lt;i>VDR&lt;/i>) gene polymorphisms are involved in asthma pathogenesis. However, accurate inflammatory mechanisms and their role in &lt;i>VDR&lt;/i> gene polymorphisms are unclear. The objective of this study was to investigate the association of &lt;i>VDR&lt;/i> gene polymorphisms, &lt;i>ApaI&lt;/i>, &lt;i>FokI&lt;/i>, &lt;i>TaqI&lt;/i>, and &lt;i>BsmI&lt;/i> with asthma as compared to controls. Children (age 5-15 years) with a history of respiratory symptoms (wheeze, shortness of breath and chest tightness) were recruited as cases. Age matched children admitted with central nervous system disorders (encephalitis/seizures) without any respiratory complaints were recruited as controls after parental consent. Children with a clinical diagnosis of cystic fibrosis, congenital heart disease and whose parents did not consent for participation in the study were excluded. &lt;i>VDR&lt;/i> gene polymorphisms were genotyped using PCR-RFLP method. One hundred and sixty asthmatics and one hundred controls were enrolled in this study. Mean age of the cases was 103.29±32.7 months and controls 94.24±30.52 months. Children with heterozygous (AC) genotype [OR=1.83, 95% CI=1.01-3.32, p=0.046] of ApaI polymorphism were found to be associated with the risk of asthma. Our findings suggest that &lt;i>ApaI&lt;/i> polymorphism of &lt;i>VDR&lt;/i> gene may contribute to asthma susceptibility among children.</pubmed_abstract><journal>International journal of molecular epidemiology and genetics</journal><pagination>24-34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8166730</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association of vitamin D receptor gene polymorphisms in North Indian children with asthma: a case-control study.</pubmed_title><pmcid>PMC8166730</pmcid><pubmed_authors>Awasthi N</pubmed_authors><pubmed_authors>Gupta S</pubmed_authors><pubmed_authors>Awasthi S</pubmed_authors><pubmed_authors>Pandey S</pubmed_authors><view_count>46</view_count></additional><is_claimable>false</is_claimable><name>Association of vitamin D receptor gene polymorphisms in North Indian children with asthma: a case-control study.</name><description>Asthma is a complex genetic disease. Vitamin D and vitamin D receptor (&lt;i>VDR&lt;/i>) gene polymorphisms are involved in asthma pathogenesis. However, accurate inflammatory mechanisms and their role in &lt;i>VDR&lt;/i> gene polymorphisms are unclear. The objective of this study was to investigate the association of &lt;i>VDR&lt;/i> gene polymorphisms, &lt;i>ApaI&lt;/i>, &lt;i>FokI&lt;/i>, &lt;i>TaqI&lt;/i>, and &lt;i>BsmI&lt;/i> with asthma as compared to controls. Children (age 5-15 years) with a history of respiratory symptoms (wheeze, shortness of breath and chest tightness) were recruited as cases. Age matched children admitted with central nervous system disorders (encephalitis/seizures) without any respiratory complaints were recruited as controls after parental consent. Children with a clinical diagnosis of cystic fibrosis, congenital heart disease and whose parents did not consent for participation in the study were excluded. &lt;i>VDR&lt;/i> gene polymorphisms were genotyped using PCR-RFLP method. One hundred and sixty asthmatics and one hundred controls were enrolled in this study. Mean age of the cases was 103.29±32.7 months and controls 94.24±30.52 months. Children with heterozygous (AC) genotype [OR=1.83, 95% CI=1.01-3.32, p=0.046] of ApaI polymorphism were found to be associated with the risk of asthma. Our findings suggest that &lt;i>ApaI&lt;/i> polymorphism of &lt;i>VDR&lt;/i> gene may contribute to asthma susceptibility among children.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2022-02-10T14:11:05.615Z</modification><creation>2022-02-10T14:11:05.615Z</creation></dates><accession>S-EPMC8166730</accession><cross_references><pubmed>34093968</pubmed></cross_references></HashMap>