143例儿童哮喘TSLP基因多态性与Eos、IgE及FeNO的关联性研究  

Association of TSLP gene polymorphisms with Eos,IgE,and FeNO in 143 pediatric asthma

作　　者：李竹梅 吴静[1] 吴贵红 蒙文娟 张亚莉[1,2] 朱晓萍 LI Zhumei;WU Jing;WU Guihong;MENG Wenjuan;ZHANG Yali;ZHU Xiaoping(School of Pediatrics,Guizhou Medical University,Guiyang 550025,China;Department of Pediatric Respiratory Medicine,Affiliated Hospital of Guizhou Medical University,Guiyang 550004,China)

机构地区：[1]贵州医科大学儿科学院,贵阳550025 [2]贵州医科大学附属医院儿童呼吸科,贵阳550004

出　　处：《免疫学杂志》2024年第4期375-382,共8页Immunological Journal

基　　金：贵州省科技厅社会发展攻关项目[黔科合支撑(2020)4Y124]。

摘　　要：目的探讨胸腺基质淋巴细胞生成素(thymic stromal lymphopoietin,TSLP)基因rs1837253、rs3806933位点多态性与儿童哮喘易感性及Eos、IgE、FeNO水平的相关性。方法选取143例哮喘儿童作为研究组,选取同期健康体检儿童112例作为对照组。采用MassARRAY SNP分型技术检测2个位点基因型,散射比浊法测定血清IgE水平,分析基因型及等位基因频率在2组间的分布差异,分析不同基因型对Eos、IgE及FeNO水平的影响。结果rs1837253等位基因及基因型频率、rs3806933等位基因频率在2组间分布无统计学差异(P>0.05);哮喘组rs3806933 CT基因型频率高于对照组,CC基因型频率低于对照组(P<0.05);与野生基因型相比,携带rs1837253 CT+CC和rs3806933 CT、CT+TT基因型的儿童患哮喘风险增高(CT+CC vs TT:OR=2.737,95%CI:1.514~4.945;CT vs CC:OR=2.058,95%CI:1.194~3.543:CT+TT vs CC:OR=1.843,95%CI:1.109~3.062)。哮喘组rs1837253位点3个基因型间Eos计数总体存在统计学差异(P<0.05,多重比较后矫正P>0.05),在对照组无统计学差异(P>0.05);2位点基因型间Eos%、IgE、FeNO及rs3806933基因型间Eos计数水平无统计学差异(P>0.05)。结论TSLP基因启动子区rs1837253、rs3806933位点多态性与儿童哮喘易感性有关,rs3806933CT基因型可能作为哮喘潜在的遗传标志物,rs1837253CT+CC、rs3806933CT+TT基因型是儿童患哮喘的风险因子;rs1837253位点多态性有影响血液Eos计数的趋势;2个SNPs与Eos%、血清IgE、FeNO水平无关。To investigate the correlation of polymorphisms at the rs1837253 and rs3806933 loci of the thymic stromal lymphopoietin(TSLP)gene with asthma susceptibility and Eos,IgE,and FeNO levels in children.A total of 143 asthmatic children were selected as the study group,and 112 healthy children undergoing routine health examinations at the same hospital were chosen as the control group.The MassARRAY SNP genotyping technology was used to detect the genotypes at two loci,while serum IgE levels were determined by using the turbidimetric scattering method.The distribution differences in genotype and allele frequencies between the two groups were analyzed,along with the effects of different genotypes on Eos,IgE,and FeNO levels.There was no statistically significant difference in the distribution of rs1837253 allele and genotype frequencies as well as rs3806933 allele frequencies between the two groups(P>0.05).However,asthma group rs3806933 CT genotype frequency was higher than the control group,and CC genotype frequency was lower than the control group(P<0.05).Compared with the wild-type genotypes,children who carried rs1837253 CT+CC and rs3806933 CT,CT+TT genotypes had an increased risk of asthma(CT+CC vs TT:OR=2.737,95%CI:1.514-4.945;CT vs CC:OR=2.058,95%CI:1.194-3.543;CT+TT vs CC:OR=1.843,95%CI:1.109-3.062).There was an overall statistical difference in Eos counts among the three genotypes at the rs1837253 locus in the asthma group(P<0.05,correction for multiple comparisons P>0.05),but not in the control group(P>0.05).There were no statistically significant differences in Eos%,IgE,and FeNO levels among the genotypes at the two loci and no significant difference in Eos counts among genotypes at the rs3806933 loci(P>0.05).Taken together,polymorphisms at rs1837253 and rs3806933 loci in the promoter region of the TSLP gene are associated with asthma susceptibility in children.rs3806933 CT genotype may serve as a potential genetic marker for asthma,and rs1837253 CT+CC and rs3806933 CT+TT genotypes are risk factors for asthma i

关 键 词：胸腺基质淋巴细胞生成素 单核苷酸多态性 嗜酸性粒细胞 免疫球蛋白E 呼出气一氧化氮 哮喘 

分 类 号：R562[医药卫生—呼吸系统]