期刊文献+

家族特应性聚集与儿童哮喘表型关系的研究 被引量:2

下载PDF
导出
摘要 目的研究家族特应性聚集与儿童哮喘表型的关系。方法对2007年4月至2008年5月本院呼吸专科就诊的216例哮喘患儿进行问卷调查及临床检查,并根据有无家族特应性疾病史分为家族特应性(A组)和无家族特应性(B组)两组,比较两组哮喘患儿特应性疾病的患病率、哮喘严重程度及血清总IgE(TIgE)、户尘螨特异性IgE(DlIgE)水平。结果A组哮喘患儿特应性患病率为81.15%,与B组45.74%比较,有显著性差异(P〈0.05);A组哮喘患儿,TIgE为(768.40±524.26)IU/mL,与B组患儿TIgE(597.16±565.38)IU/mL相比较,有显著性差异(P〈0.05);A组哮喘患儿DlIgE为(62.35±51.14)kua/L,与B组患儿D1IgE(59.43±60.77)kua/L相比较,无显著性差异(P〉0.05);A组哮喘患儿重度哮喘患病率为10.66%,与B组的重度哮喘患病率3.19%比较,有显著性差异(P〈0.05);A组哮喘患儿中度哮喘患病率为30.33%,与B组的中度哮喘患病率12.77%比较,有显著性差异(P〈0.05);两组患儿间歇发作、轻度哮喘患病率分别比较,无显著性差异(P均〉0.05)。重度哮喘患儿TIgE(1326.04±635.48)IU/mL,与非重度哮喘患儿TIgE(650.05±539.10)IU/mL相比较,差异有统计学意义(P〈0.05)。结论家族特应性聚集与患儿哮喘表型之间有一定的关系,有家族特应性聚集的哮喘息儿易患特应性疾病,病情较严重,TIgE水平更高。 Objective To investigate the relationship between familial aggregation of atopy and asthma phenotypes in children. Methods A total of 216 cases with asthma were asked to complete the asthma questionnaires and receive physical examination, and then according to the familial predisposition divided into two groups to compare atopic disease incidence, asthma severity and the level of serum IgE (TIgE) and Dust mite specificity IgE(DIIgE). Result Positive familial predisposition group, the attack rate of atopic disease in children was 81.15 %, had significant difference than negative family predisposition group 45.74 % ( P 〈 0.05) ; positive family predisposition group, TIgE of asthma children was 768.40 ± 524.26IU/mL, had significant difference than negative family predisposition group 597.16 ± 565.38 IU/mL ( P 〈 0.05) ; positive family predisposition group, DIlgE of asthma children was 62.35 ± 51.14kua/L, hadn' t significant difference than negative family predisposition group 59.43 ± 60.77kua/L( P 〉 0.05) ; positive family predisposition group, the attack rate of severe persistent in children was 10.66%, had significant difference than negative family predisposition group 3.19% ( P 〈 0.05 ); positive family predisposition group, the attack rate of moderate persistent in children was 30.33%, had significant difference than negative family predisposition children 12.77 % ( P 〈 0.05); Attack rate of intermittent and mild persistent asthma in two groups hadn' t significant difference (P 〉0.05, respectively). TIgE of severe persistent asthma children was 1326.04 ± 635.48 IU/mL, had significant difference than Non- Severe Persistent 650.05 ± 539.10IU/mL ( P 〈 0.05). Conclusion Family aggregation of atopy is associated with asthma phenotypes in children: Positive family predisposition of atopy pre - dispose asthma children to atopic disease, and their pathogenetie condition is worse, TIgE level is higher.
出处 《浙江临床医学》 2009年第1期24-27,共4页 Zhejiang Clinical Medical Journal
关键词 哮喘表型 家族史 过敏症 患儿 Asthma phenotypes Familial predisposition Allergy Children
  • 相关文献

参考文献9

  • 1Los H, Postrnus PE, Boomsma DI. Asthma genetics and intermediate phenotypes: a review from twin studies. Twin Res,2001,4:81 - 93.
  • 2Burke W, Fesinmeyer M, Reed K, et al. Family history as a predict or of asthma risk. Am J Prey Med,2003,24:160- 169.
  • 3Lima JJ. Treatment heterogeneity in asthma: genetics of response to leukotriene modifiers. Mol Diagn The, r, 2007,11(2):97- 104.
  • 4Burrows B, Martinez FD, Halonen M, et al. Association of asthma with serum total IgE levels and skin2test reactivity to allergens. N Engl J Med, 1989,320(5) :271 - 277.
  • 5Meyers DA, Beaty TH, Colyer CR, et al. Genetics of total serum IgE level: a regressive model approach to segregation analysis. Genet Epidemiol, 1991,8(5) : 351 - 359.
  • 6Fukunaga J, Abe M, et al. Comparative study to elucidate the mechanism underlying the difference in airway hyperresponsiveness between two mouse strains. Int Immunopharmacol,2007,7(14) : 1852-1861.
  • 7Barnes PJ. Cytoldne modulators as novel therapies for asthma. Annu Rev Pharmacol Toxicol,2002,42:81 -98.
  • 8Doull J M, Lawrence S, Waton M, et al. Allelic association of genemairkers on chromosomes 5q and 11 q with atopy and bron-chial hyperresponsiyeness. AMJ Resp ir Critcare Med, 1996, 153:1280-1284.
  • 9安肃英,孙宗芝,李根山.哮喘儿童血免疫球蛋白E、T细胞亚群与细胞因子动态观察及临床意义[J].实用儿科临床杂志,2004,19(2):117-119. 被引量:44

二级参考文献6

共引文献43

同被引文献16

  • 1朱万春,诸葛洪祥.粉螨性哮喘发病机制研究进展[J].环境与健康杂志,2007,24(3):184-186. 被引量:16
  • 2Zhang J, Paré PD, Sand ford AJ.Reeent advances in asthma genetics [J]. Respir Res ,2008,9:4.
  • 3Fukai H,Ogasawara Y, Migita O, et al. Association between a polymorphism in cysteinyl leukotriene receptor 2 on chromosome 13q14 and atopic asthma[ J ]. Pharmacogenetics ,2004,14 ( 10 ) :683 - 690.
  • 4Woszczek G, Chen LY, Nagineni S, et al. Leukotriene D (4) induces gene expression in human monocytes through cysteinyl leukotriene type I receptor[ J]. J Allergy Clin lmmuno1,2008,121 ( 1 ) :215 - 221.
  • 5Arriba - Mendez S, Sanz C, Isidoro - Garcia M,et al. 927T > C polymorphism of the cysteinyl - leukotriene type - 1 receptor (CYSLTR1) gene in children with asthma and atopic dermatitis[ J ]. Pediatr Allergy Immunol,2006,17 ( 5 ) :323 - 328.
  • 6Arriba - M6ndez S, Sanz C, Isidoro - Garcia M, et al. Analysis of 927T >C CYSLTR1 and -444A > C LTC4S polymovphisms in children with asthma [ J ]. AUergol Immunopathol (Madr) , 2008,36 ( 5 ) : 259 - 263.
  • 7Kim SH, Oh JM, Kim YS,et al. Cysteinyl leukotriene receptor 1 promoter polymorphism is associated with aspirin - intolerant asthma in males [ J ]. Clin Exp Allergy,2006,36 (4) :433 - 439.
  • 8Thompson MD,Capra V,Takasaki J,et al. A functional G300S variant of the eysteinyl leukotriene 1 receptor is associated with atopy in a Tristan da Cunha isolate [ J ]. Pharmacogenet Genomics ,2007,17 (7) :539 - 549.
  • 9Hong X ,Zhou H, Tsai HJ, et al. Cysteinyl leukotriene receptor 1 gene variation and risk of asthma [ J ]. Eur Respir J,2009,33 ( 1 ) :42 - 48.
  • 10Bisgaard H, Halkjaer LB, Hinge R, et al. Risk analysis of early childhood eczema [ J ]. J Allergy Clin lmmunol, 2009, 123 ( 6 ) : 1355 - 1360.

引证文献2

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部