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ADAM33基因多态性与新疆汉族哮喘的相关性研究 被引量:1

Association between single nucleotide polymorphisms of rs511898 of ADAM33 gene and bronchia asthma in Xinjiang Han population
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摘要 目的:探讨新疆汉族支气管哮喘与ADAM33基因rs511898位点多态性的关系。方法:采用聚合酶链反应和限制片段长度多态性(PCR-RFLP)方法对63例新疆汉族支气管哮喘患者病例组和70例无血缘关系的健康对照组进行ADAM33基因rs511898位点单核苷酸多态性(SNP)分析。结果:ADAM33基因rs511898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rs511898位点的基因型频数分布:GA为31(34.6),GG为28(24.2),AA为4(4.3),对照组该位点基因型频数分布为GA为42(38.4),GG为23(26.8),AA为5(4.7),2组间基因型频数分布无统计学意义(P>0.05)。G、A等位基因频数分布在2组间比较差异无统计学意义(P>0.05)。结论:ADAM33基因rs511898位点等位基因突变与新疆汉族支气管哮喘的发生没有明显的关联性。 Objective: To investigate the genetic association of bronchial asthma with ADAM33 gene polymorphism in Xinjiang Han population. Methods: PCR-RFLP were used to examine the single nucleotide polymorphism (SNP) of ADAM33 gene in 63 with bronchial asthma (case group) and 70 healthy individuals (control group). Results: The genotype distributions on rs511898 of ADAM33 gene in case group and control group did not deviate from Hardy-Weinberg equilibrium. The frequency distribution of rs511898 in case group as follows: 31 were GA (34; 6), 28 were GG (24.2), 4 were AA (4.3) ; the frequency distributions on rs511898 in control group as follows: 42 were GA (38.4), 23 was GG (26.8), 5 were AA (4.7). 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 A and G between two groups either (P〉0.05). Conclusion: The mutant allele of rs511898 of ADAM33 gene may not be associated with bronchial asthma in Xinjiang Han population.
出处 《新疆医科大学学报》 CAS 2009年第6期701-703,共3页 Journal of Xinjiang Medical University
关键词 哮喘 ADAM33基因 单核苷酸多态性 Asthma ADAM33 single gene polymorphism
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参考文献7

  • 1Weiss ST, Raby BA. Asthma genetics 2003 [J]. Hum Mol Genet, 2004,13 :R83-89.
  • 2支气管哮喘防治指南(支气管哮喘的定义、诊断、治疗和管理方案)[J].中华结核和呼吸杂志,2008,31(3):177-185. 被引量:2518
  • 3Cheng L, Enomoto T, Hirota T, et al. Polymorphisms in ADAM33 are associated with allergic rhinitis due to Japanese cedar pollen[J]. Clin Exper Aller, 2004,34 : 1192-1201.
  • 4HowardTD, Postma DS, Jongepier H, et al. Association of a disintegrin and metalloprotease33(ADAM33) gene with asthma in ethnically diverse populations[J]. Aller Clin Immunol, 2003,112(4) : 717-722.
  • 5Van Eerdewegh P, Little RD, Dupuis J, et al. Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness[J]. Nature , 2002,418 : 426-430.
  • 6邱玉明,罗雅玲,赖文岩,邱士军,吴月仙.ADAM33基因Met764Thr位点多态性与支气管哮喘发病及患者肺功能的相关性[J].中华结核和呼吸杂志,2007,30(7):518-521. 被引量:22
  • 7Wang P,Liu QJ,Li JS,et al. Lack of association between AD- AM33 gene and asthma in a Chinese population[J].Int J Immunogene, 2006,33(4) :303-306.

二级参考文献9

  • 1Van Eerdewegh P, Little RD, Dupuis J, et al. Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature,2002,418:426-430.
  • 2Werner M, Herbon N, Gohlke H, et al. Asthma is associated with single-nucleotide polymorphisms in ADAM33. Clin Exp Allergy, 2004,34:26-31.
  • 3Lee JH, Park HS, Park SW, et al. ADAM33 polymorphism: association with bronchial hyper-responsiveness in korean asthmatics. Clin Exp Allergy,2004,34:860-865.
  • 4Wolfsberg TG, Primakoff P, Myles DG, et al. ADAM, a novel family of membrane proteins containing a disintegrin and metalloprotease domain: muhipotential functions in cell-cell and cell-matrix interactions. J Cell Biol, 1995,131:275-278.
  • 5Yoshinaka T, Nishii K, Yamada K, et al. Identification and characterization of novel mouse and human ADAM33s with potential metalloprotease activity. Gene,2002,282:227-236.
  • 6Hirota T, Hasegawa K, Obara K, et al. Association between ADAM33 polymorphisms and adult asthma in the Japanese population. Clin Exp Allergy ,2006,36:884-891.
  • 7Jongepier H, Boezen HM, Dijkstra A, et al. Polymorphisms of the ADAM33 gene are associated with accelerated lung function decline in asthma. Clin Exp Allergy,2004,34:757-760.
  • 8Simpson A, Maniatis N, Jury F, et al. Polymorphisms in a disintegrin and metalloprotease 33 ( ADAM33 ) predict impaired early-life lung function. Am J Respir Crit Care Med ,2005,172:55- 60.
  • 9中华医学会呼吸病学分会哮喘学组.支气管哮喘防治指南(支气管哮喘的定义、诊断、治疗及教育和管理方案)[J].中华结核和呼吸杂志,2003,26(3):132-138. 被引量:3564

共引文献2535

同被引文献25

  • 1汤彦,许振华,吴晓琴,李月琴,周天鸿.白细胞介素4受体α链基因多态性与支气管哮喘的相关性研究[J].中华结核和呼吸杂志,2006,29(7):440-443. 被引量:9
  • 2邱玉明,罗雅玲,赖文岩,邱士军.中国华南地区汉族人群支气管哮喘患者ADAM33基因T_1位点多态性研究[J].南方医科大学学报,2007,27(4):485-487. 被引量:5
  • 3Moffatt MF, Kabesch M, Liang L, et al. Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature, 2007, 448:470-473.
  • 4Ober C, Tan Z, Sun Y, et al. Effect of variation in CHBL1 on serum YKL-40 level, risk of asthma, and lung function [ J ]. N Engl J Med, 2008, 358 : 1682-1691.
  • 5Gudbjartsson DF, Bjornsdottir US, Halapi E, et al. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat Genet, 2009, 41:342-347.
  • 6Himes BE, Hunninghake GM, Baurley JW, et al. Genome-wide association analysis identifies PDEAD as an asthma-susceptibility gene. Am J Hum Genet, 2009, 84:581-593.
  • 7Vercelli D. Discovering susceptibility genes for asthma and allergy. Nat Rev Immunol, 2008, 8(3) :169-182.
  • 8Van Eerdewegh P, Little R D, Dupuis J, et al. Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature, 2002, 418:426430.
  • 9Foley SC, Mogas AK, Olivenstein R, et al. Increased expression of ADAM33 and ADAM8 with disease progression in asthma. J Allergy Clin Immunol, 2007,119 : 863-871.
  • 10Howard TD, Postma DS, Jongepier H, et al. Association of a disintegrin and metalloprotease 33 ( ADAM33 ) gene with asthma in ethnically diverse populations. J Allergy Clin Immunol, 2003, 112:717-722.

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