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GPRA基因rs324374位点基因多态性与儿童支气管哮喘的关系 被引量:1

Association between GPRA gene polymorphism and bronchial asthma in children
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摘要 目的:探讨中国北方汉族儿童支气管哮喘易感性与哮喘相关G蛋白偶联受体(GPRA)基因多态性的关系。方法:采用PCR和限制性片段长度多态性(RFLP)方法检测中国北方117例支气管哮喘患儿和121例健康对照儿童GPRA基因rs324374位点基因多态性。结果:GPRA基因rs324374位点病例组和对照组中基因型分布均符合Hardy-Weinberg平衡定律;病例组rs324374位点的基因型频数分布:CC为22(18.80%),CT为66(56.40%),TT为29(24.80%),对照组该位点基因型频数分布分别为CC为30(24.79%),CT为61(50.42%),TT为30(24.79%),2组间基因型频数分布无显著性差异(P>0.05);C、T等位基因频数分布在2组间比较差异无显著性(P>0.05)。结论:GPRA基因rs324374位点等位基因突变与儿童支气管哮喘的发生没有明显的关联性。 Objective To investigate the association of susceptibility of bronchial asthma with GPRA gene polymorphism in North Chinese Han children. Methods The techniques of PCR and restriction fragment polymorphism (RFLP) were used to examine single nucleotide polymorphisms (SNPs) on rs324374 of GPRA gene in 117 children with bronchial asthma ( case group ) and 121 healthy individuals ( control group). Results The genotype distributions on rs324374 of GPRA gene in case group and control group did not deviate from Hardy- Weinberg equilibrium. The frequency distribution of rs324374 in case group as follows: 22 were CC (18.80%), 66 were CT (56.40%), 29 were TT (24.80%); the frequency distributions on rs324374 in control group as follows: 30 were CC (24.79%), 61 was CT (50.42%), 30 were TT (24. 79%) . And there was no significant difference of frequency distribution of three genotypes between case group and control group (P〉0. 05) and there was no significant difference of frequency distribution of allele C and T between two groups either (P〉 0. 05). Conclusion The mutant allele of rs324374 of GPRA gene may not be associated with bronchial asthma in children.
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2007年第3期546-548,573,共4页 Journal of Jilin University:Medicine Edition
基金 国家自然科学基金资助课题(30370669)
关键词 儿童 哮喘 哮喘相关G蛋白偶联受体 多态性 单核苷酸 疾病遗传易感性 child asthma G-protein coupled receptor related to asthma polymorphism, single nucleotide genetic predisposition to disease
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参考文献6

  • 1刘丽,鲁继荣,成焕吉,邹映雪.β_2肾上腺素能受体基因与小儿哮喘的关系[J].吉林大学学报(医学版),2004,30(2):259-260. 被引量:6
  • 2Laitinen T,Polvi A,Rydman P,et al.Characterization of a common susceptibility locus for asthma-related traits[J].Science,2004,304:300-304.
  • 3李波,韩宏志,李善玉,史杰萍,何海涛,孔宁,刘娅.亚甲基四氢叶酸还原酶基因多态性与儿童支气管哮喘的相关性[J].疾病控制杂志,2005,9(6):548-550. 被引量:3
  • 4Vendelin J,Pulkkinen V,Rehn M,et al.Characterization of GPRA a novel G protein-coupled receptor related to asthma[J].Am J Respir Cell Mol Biol,2005,33:262-270.
  • 5Melen E,Bruce S,Doekes G,et al.Haplotypes of G protein-coupled receptor 154 are associated with childhood allergy and asthma[J].Am J Respir Crit Care Med,2005,171:1089-1095.
  • 6Kormann MS,Carr D,Klopp N,et al.G protein-coupled receptor polymorphisms are associated with asthma in a large German population[J].Am J Respir Crit Care Med,2005,171:1358-1362.

二级参考文献13

  • 1全国儿科哮喘防治协作组.儿童哮喘防治常规(1998年修订)[J].中华儿科杂志,1998,36(12):748-748.
  • 2叶任高.内科学[M](第5版)[M].北京:人民卫生出版社,2001.824.
  • 3Ligget SB. Molecular and genetic basis of beta 2 Adrenergic receptor function [J]. J Allergy Clin Immunol, 1999,104 (2pt2) :s42-46.
  • 4Israel E, Drazen JM, Liggett SB, et al. The effect of polymorphism of the β2-adrenergic receptor to regular use of albuteral in asthma [J]. Int Arch Allergy Immunol, 2001, 124 (1): 183-186.
  • 5Kowalski ML, Woszczek G, Borowiee M, et al. Distribution of the β2-adrenergic receptor polymorphisms in atopic and nonatopic patients [J]. J Allergy Clin Immunol, 1997. 100 (3):338-340.
  • 6邰风.一种常见的甲烯四氢叶酸还原酶基因突变的世界性分布[J].国外医学:遗传学分册,1999,22(2):110-110.
  • 7Botto LD, Yang Q. 5, 10-methylenetetrahydrofolate reductase gene variants and congenital anomalies: a Hu GE review [J ]. Am J Epidemiol, 2000,151: 862-877.
  • 8Zou C, Tsukahara H, Hiraoka M, et al. Methylenetetrahydr-ofolate reductase polymorphism in childhood primary focal segmental glomerulosclerosis [J]. Nephron, 2002,92(2):449-451.
  • 9Kang SS. Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations [J]. Am J Hum Genet, 1991,48(3) :546-551.
  • 10Desai A, Lankford HA, Warren JS. Homocysteine augments cytokine-induced chemokine expression in human vascular smooth muscle cells: implications for atherogenesis [J ]. Inflammation,2001,25(3): 179-186.

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