期刊文献+

蒙古族儿童过敏性紫癜及其器官损害与HLA-DRB1等位基因的关联性 被引量:3

Correlation between HLA-DRB1 allele and anaplylactoid purpura as well as impairments of organs in juvenile of Mongolian
原文传递
导出
摘要 目的探索内蒙地区蒙古族儿童过敏性紫癜(AP)及其累及肾脏、胃肠道和关节与HLA-DRB1等位基因的关联性。方法引入PCR-SSP技术,在内蒙地区同是蒙古族但无血缘关系或蒙古族与其他民族间无通婚史及其他风湿性疾病史和家族史的蒙古族人群中,收集AP病例57例,其中累及肾脏20例、胃肠道29例和关节26例,分别与102名健康儿童的HLA-DRB1等位基因进行型别分析。组间比较在单因素χ2检验的基础上,作以多因素Logistic回归分析。结果HLA-DRB1*110x等位基因在AP及其累及关节、*070x等位基因在累及胃肠道分别与对照组经Logistic回归分析,均P<0.05,差异有显著意义。B均为正值,OR分别是2.251、2.215和2.552,均>1,与B值相符,95%可信区间内均不包含1。表明排除其他进入模型的等位基因作用外,DRB1*110等位基因在AP及其累及关节、*070x等位基因累及胃肠道的致病优势分别是对照组的2.251、2.215和2.552倍,促进发病。EF均>0;而DRB1*040x和*120x等位基因在AP病例组分别与对照组经Logistic回归分析,均P<0.05,差异有显著意义。B均为负值,OR分别是0.422和0.424,均<1,与B值相符,95%可信区间内均不包含1。表明排除其他进入模型等位基因作用外,DRB1*040x和*120x等位基因在AP病例组致病优势分别是对照组的0.422和0.424倍,阻止发病。PF均>0。结论HLA-DRB1*110x等位基因可能为内蒙地区蒙古族儿童AP及其累及关节、*070x等位基因为累及胃肠道发病单体型中的遗传易感基因,而DRB1*040x和*120x等位基因为AP的遗传保护基因。 Objective To explore the correlation between HLA-DRB1 allele and anaphylactoid purpura(AP) and its association with kidney,gastrointestinal and joint in juvenile of Mongolian residing in Inner Mongolia. Methods We collected 57 Mongolian children with AP,who had been residing in lnner Mongolia three generations,had not kinship,intermarriage background,other medical history and family history of rheumatic with each other,20 of them involing kidney, 29 involving gastrointestinal, 26 involving joint and compared rheir polymorphism of HLA- DRB1 allele with 102 health children' s respectively, and leaded into PCR-SSP technigne. The comparing between group and group was dealt with by logistic regression after one-way X^2 test. Results The logistic regression between HLA-DRB1 110x allele in AP and its association with joint, 070x allele in involving gastrointestinal and control group respectively were dealt with. P 〈 0.05 for all, the deffirence had statistical significance. B were positive for all, OR were 2.251,2.215 and 2. 552 respectively, all〉 1, whose 95 % confident interval didn' t include 1 for all. It indicated that the led to disease odds of DILB1 * 110x allele in AP and its association with joint, * 070x allele in involving gastrointestinal were 2. 251,2. 215 and 2. 552 times of control group respectively except for action of other alleles of get into pattern,and it was led to pathogenesis. EF were 〉 0 for all, While the Logistic regression between DRB1*040x and* 120x alleles in AP and control group respectively were dealt with. P were 〈 0.05 for all, the deffirence had statistical significance. B were negative for all, OR were 0. 422 and 0. 424 respectively, all 〈 1, whose 95 % confident intervol didn't include 1 for all. It's indicated that the led to disease odds of DRB1*040x and 120x allele in AP were 0. 422 and 0. 424 times of control group respectively except action of other alleles of get into pattern,and It was protective pathogenesis. PF were 〉 0 for all. Conclusion The allele of HLA-DRB1 * 110x may be a susceptible gent in AP and its associated with joint and ** 070x is a susceptible gene in AP associated with gastoointestinal;While the alleles of DRB1 * 040x and * 120x are the protective ones in AP of children who are Mongolian inhabitations in Inner Mongolia.
出处 《中国基层医药》 CAS 2005年第12期1659-1661,共3页 Chinese Journal of Primary Medicine and Pharmacy
基金 内蒙古科委自然科学基金(990302-1)
关键词 儿童 亚洲大陆世系人群 蒙古族 过敏性紫癜 器官损害 HLA-DRB1 等位基因 Purpura, schoen lein-henock Children Asian continental ancestry group Alleles
  • 相关文献

参考文献7

  • 1胡亚美 江载芳 等 主编.诸福棠实用儿科学(第7版)[M].北京:人民卫生出版社,2002.458~461.
  • 2Olerup O,Zetterquist H. HLA-DR typing by PCR amplification with sequence-specific primers(PCR-SSP) in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation. Tissue Antigen, 1992, 39:225-235.
  • 3熊平,扬颖,龚非力.一种新的HLA─Ⅱ类基因分型方法——PCR/SSP技术的建立[J].免疫学杂志,1996,12(4):258-261. 被引量:41
  • 4韩秀萍,张志欣,肖毅,宋芳吉,李伟,贺为东,李惠刚,单晓艳,阎焕东.北方汉族过敏性紫癜与HLA相关性研究[J].中华医学遗传学杂志,1997,14(2):79-81. 被引量:10
  • 5Jin DK, Kohsaka T, Koo JW, et al. Complement 4 locus, Ⅱ gene deletion and DQA1 * 0301 gene: genetic risk factors for lgA nephropathy and Henoch-Schonlein nephritis. Nephron, 1996, 73:390-395.
  • 6Amoroso A,Berrino M,C.anale L, el a]. Immunogenetics of Henoch-Schoenlein desease. European Journal of Immunogenetics, 1997,24 :323-333.
  • 7Amoli MM,Thomson W,Hajcer AH,el al. HLA-DRB1 * 01 association with Henoch-Schonlein purpura in patients from northwest spain. Journal of Rheumatology, 2001,28 :1266-1270.

二级参考文献7

  • 1李哲光,中国免疫学杂志,1994年,10卷,5期,317页
  • 2林万明,临床基因探针诊断实验技术,1993年
  • 3黄培堂,PCR技术的原理和应用,1990年
  • 4赵桐茂,HLA分型原理和应用,1984年
  • 5杨国亮,皮肤病学,1991年,616页
  • 6宋芳吉,生理科学,1988年,8卷,4期,204页
  • 7田军,中华肾脏病杂志,1985年,1卷,2期,87页

共引文献332

同被引文献51

  • 1刘志强,邬丽莎.新视角──HLA及其与人类疾病的相关性研究进展[J].中国全科医学,2004,7(17):1268-1271. 被引量:3
  • 2任少敏,刘向梅,保明利,王继春,仝林虎,李维才.HLA-DQA1基因与小儿支气管哮喘及其严重程度的相关性研究[J].中国基层医药,2007,14(4):529-532. 被引量:2
  • 3Amoroso A, Danek G, Vatta S, et al. Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients. Nephrol Dial Transplant, 1998, 13(12) :3184-3188.
  • 4Dudley J, Afifi E, Gardner A, et al. Polymorphism of the ACE gene in Henoch-Schonlein purpura nephritis. Pediatr Nephrol,2000,14(3) :218-220.
  • 5Brodkiewicz A, Ciechanowicz A, Urbanska A, et al. The I/D polymorphism of the ACE gene in children with Henoch-Schoenlein purpura. Pol Merkuriusz Lek,2000,8(46) :236-238.
  • 6Ozkaya O, Soylemezoglu O, Gonen S, et al. Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement. Clin Rheumatol, 2006,25 (6) : 861-865.
  • 7Amoli MM,Thomson W, Hajeer AH,et al.HLA-B35 association with nephritisin Henoch-Schonlein purpura. J Rheumatol, 2002,29 (5) : 948-949.
  • 8Amoli MM, Thomson W, Hajee: AH, et al. HLA-DRB1 * 01 association with Henoch-Schonlein purpurain patients from northwest Spain. Rheumatology, 2001,28(6) : 1266-1270.
  • 9Stefansson Thors V, Kolka R, Sigurdardottir SL, et al. Increased frequency of CAB * Q0 alleles in patients with Henoch-Schonlein purpura. Scand J Immunol, 2005,61 (3) : 274-278.
  • 10刘志红 杨俊伟 陈朝红 等.Gene polymorphism in IL-1 receptor antagonist affects its production by monocytes in IgA nephropathy and Henoch-Schonlein nephritis[J].Chinese Medical Journal(中华医学杂志:英文版),2001,114(12):1313-1316.

引证文献3

二级引证文献4

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