首页 | 本学科首页   官方微博 | 高级检索  
检索        

维生素D缺乏性佝偻病遗传易感性的研究
引用本文:吴胜虎,余晓丹,颜崇淮,沈理笑,余晓刚,张燕萍,张劲松,金星明,沈晓明.维生素D缺乏性佝偻病遗传易感性的研究[J].中国当代儿科杂志,2006,8(2):121-124.
作者姓名:吴胜虎  余晓丹  颜崇淮  沈理笑  余晓刚  张燕萍  张劲松  金星明  沈晓明
作者单位:吴胜虎,余晓丹,颜崇淮,沈理笑,余晓刚,张燕萍,张劲松,金星明,沈晓明
基金项目:上海市重点学科建设项目;上海市高等学校青年科学基金
摘    要:目的:遗传因素是否参与维生素D缺乏性佝偻病目前尚未明了。拟通过研究维生素D受体基因多态性与维生素D缺乏性佝偻病易感性的相关性,探讨维生素D缺乏性佝偻病的遗传易感性。方法:应用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析技术检测159例维生素D缺乏性佝偻病儿童和78例正常儿童(对照组)维生素D受体(VDR)基因FokI位点的多态性,比较两组之间VDR基因型和等位基因的频率。结果:维生素D缺乏性佝偻病患儿和对照组儿童的VDR基因FokI位点基因型分布频率分别为:FF(37%),Ff(51%),ff(12%)和FF(18%),Ff(55%),ff(27%),两组之间的差异有显著性(χ20.01(2)=9.210,χ2=13.3880,P<0.01);佝偻病患儿和对照组儿童的VDR基因FokI位点等位基因分布频率分别为:F(63%),f(37%)和F(46%),f(54%),两组之间的差异有显著性(χ2=6.18,P<0.05)。佝偻病患儿F等位基因分布频率明显高于对照组人群(63%vs46%)两组之间的差异有显著性;而佝偻病患儿f等位基因频率显著低于对照组(37%vs 54%)。结论:VDR基因FokI酶切位点的多态性可能与维生素D缺乏性佝偻病的遗传易感性有关。

关 键 词:维生素D受体  基因多态性  维生素D缺乏性佝偻病  儿童  
文章编号:1008-8830(2006)02-0121-04
收稿时间:2005-09-27
修稿时间:2005-11-28

Association between vitamin D receptor gene polymorphism and vitamin D deficiency rickets
WU Sheng-Hu,YU Xiao-Dan,YAN Chong-Huai,SHEN Li-Xiao,YU Xiao-Gang,ZHANG Yan-Ping,ZHANG Jin-Song,JIN Xing-Ming,SHEN Xiao-Ming.Association between vitamin D receptor gene polymorphism and vitamin D deficiency rickets[J].Chinese Journal of Contemporary Pediatrics,2006,8(2):121-124.
Authors:WU Sheng-Hu  YU Xiao-Dan  YAN Chong-Huai  SHEN Li-Xiao  YU Xiao-Gang  ZHANG Yan-Ping  ZHANG Jin-Song  JIN Xing-Ming  SHEN Xiao-Ming
Institution:WU Sheng-Hu, YU Xiao-Dan, YAN Chong-Huai, SHEN Li-Xiao, YU Xiao-Gang, ZHANG Yan-Ping, ZHANG Jin-Song, JIN Xing-Ming, SHEN Xiao-Ming
Abstract:OBJECTIVE: To explore the genetic susceptibility of children to vitamin D deficiency rickets through studying the association between Vitamin D receptor (VDR) gene polymorphism and vitamin D deficiency rickets. METHODS: One hundred and fifty-nine children (100 boys and 59 girls, aged 0 to 2 years), with new-onset vitamin D deficiency rickets were enrolled. The patients sampled from a community of Jiamusi City, Heilongjiang Province. Seventy-eight healthy age-matched children (46 boys and 32 girls) were used as the controls. VDR gene polymorphism (cleaved by restriction endonuclease Fok I) was analyzed by polymerase chase reaction-restriction fragment length polymorphism (PCR-RFLP). The frequencies of the VDR genotype and allele were compared between the two groups. RESULTS: The frequencies of FF, Ff and ff genotypes were 37%, 51% and 12% in the Rickets group, and 18%, 55% and 27% in the Control group. A significant difference was found in the frequency distribution of the VDR genotype between the two groups (chi(2)(0.01(2))=9.210, chi(2)=13.3880, P < 0.01). In the Rickets group, f allele frequency was lower (37% vs 54%), while the F allele was more common than the Control group (63% vs 46%). CONCLUSIONS: There is an association between the VDR gene Fok I polymorphism and vitamin D deficiency rickets. The individuals with the F allele are more susceptible to vitamin D deficiency rickets.
Keywords:Vitamin D receptor  Polymorphism  Vitamin D deficiency tickets  Child
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国当代儿科杂志》浏览原始摘要信息
点击此处可从《中国当代儿科杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号