北印度哮喘儿童维生素D受体基因多态性的相关性:一项病例对照研究。

International journal of molecular epidemiology and genetics Pub Date : 2021-04-15 eCollection Date: 2021-01-01
Nidhi Awasthi, Shally Awasthi, Shivani Pandey, Sarika Gupta
{"title":"北印度哮喘儿童维生素D受体基因多态性的相关性:一项病例对照研究。","authors":"Nidhi Awasthi,&nbsp;Shally Awasthi,&nbsp;Shivani Pandey,&nbsp;Sarika Gupta","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Asthma is a complex genetic disease. Vitamin D and vitamin D receptor (<i>VDR</i>) gene polymorphisms are involved in asthma pathogenesis. However, accurate inflammatory mechanisms and their role in <i>VDR</i> gene polymorphisms are unclear. The objective of this study was to investigate the association of <i>VDR</i> gene polymorphisms, <i>ApaI</i>, <i>FokI</i>, <i>TaqI</i>, and <i>BsmI</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. <i>VDR</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 <i>ApaI</i> polymorphism of <i>VDR</i> gene may contribute to asthma susceptibility among children.</p>","PeriodicalId":73460,"journal":{"name":"International journal of molecular epidemiology and genetics","volume":"12 2","pages":"24-34"},"PeriodicalIF":0.0000,"publicationDate":"2021-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166730/pdf/ijmeg0012-0024.pdf","citationCount":"0","resultStr":"{\"title\":\"Association of vitamin D receptor gene polymorphisms in North Indian children with asthma: a case-control study.\",\"authors\":\"Nidhi Awasthi,&nbsp;Shally Awasthi,&nbsp;Shivani Pandey,&nbsp;Sarika Gupta\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Asthma is a complex genetic disease. Vitamin D and vitamin D receptor (<i>VDR</i>) gene polymorphisms are involved in asthma pathogenesis. However, accurate inflammatory mechanisms and their role in <i>VDR</i> gene polymorphisms are unclear. The objective of this study was to investigate the association of <i>VDR</i> gene polymorphisms, <i>ApaI</i>, <i>FokI</i>, <i>TaqI</i>, and <i>BsmI</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. <i>VDR</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 <i>ApaI</i> polymorphism of <i>VDR</i> gene may contribute to asthma susceptibility among children.</p>\",\"PeriodicalId\":73460,\"journal\":{\"name\":\"International journal of molecular epidemiology and genetics\",\"volume\":\"12 2\",\"pages\":\"24-34\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166730/pdf/ijmeg0012-0024.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of molecular epidemiology and genetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of molecular epidemiology and genetics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

哮喘是一种复杂的遗传疾病。维生素D和维生素D受体(VDR)基因多态性与哮喘发病有关。然而,准确的炎症机制及其在VDR基因多态性中的作用尚不清楚。本研究的目的是研究与对照组相比,VDR基因多态性、ApaI、FokI、TaqI和BsmI与哮喘的关系。有呼吸系统症状(喘息、呼吸短促和胸闷)病史的儿童(5-15岁)被招募为病例。经父母同意后,招募年龄匹配的无任何呼吸系统疾病的中枢神经系统疾病(脑炎/癫痫发作)儿童作为对照组。临床诊断为囊性纤维化、先天性心脏病且父母不同意参与研究的儿童被排除在外。采用PCR-RFLP方法对VDR基因多态性进行基因分型。160名哮喘患者和100名对照者参加了这项研究。患者平均年龄103.29±32.7个月,对照组平均年龄94.24±30.52个月。ApaI基因多态性为杂合型(AC)的儿童[OR=1.83, 95% CI=1.01-3.32, p=0.046]与哮喘发病风险相关。本研究提示,VDR基因ApaI多态性可能与儿童哮喘易感性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Association of vitamin D receptor gene polymorphisms in North Indian children with asthma: a case-control study.

Asthma is a complex genetic disease. Vitamin D and vitamin D receptor (VDR) gene polymorphisms are involved in asthma pathogenesis. However, accurate inflammatory mechanisms and their role in VDR gene polymorphisms are unclear. The objective of this study was to investigate the association of VDR gene polymorphisms, ApaI, FokI, TaqI, and BsmI 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. VDR 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 ApaI polymorphism of VDR gene may contribute to asthma susceptibility among children.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Exploring the effects of homocysteine metabolism in osteoporosis management in Indian adult females. P. falciparum genetic markers associated with drug resistance from patients with treatment failure in the Southern part of Senegal in 2017. Abundance and diversity of methicillin-resistant bacteria from bathroom surfaces at workplaces using CHROMagar media, 16S, and dnaJ gene sequence typing. Analysis of carbapenem-resistant Acinetobacter baumannii carbapenemase gene distribution and biofilm formation. Facial and ocular manifestations of male patients affected by the HUWE1-related intellectual developmental disorder.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1