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作 者:刘梅[1] 李海林[1] 黄永坤[1] 陈燕华[1] 刘华[2] 金萍[1]
机构地区:[1]昆明医学院第一附属医院儿科,云南昆明650032 [2]昆明医学院第一附属医院检验科PCR实验室,云南昆明650032
出 处:《中国优生与遗传杂志》2005年第11期20-23,共4页Chinese Journal of Birth Health & Heredity
摘 要:目的探讨RANTES单核苷酸多态性(SNP)与哮喘易感惠儿的相关性。方法 采用聚合酶链反应方法对32例哮 喘患儿和32例正常对照进行了RANTES-403及-28位点基因型分布和等位基因频率研究。结果 病例组RANTES-403位 点G/G、G/A、A/A基因型频率分别为53.13%、40.62%、6.25%;对照组分别为50.00%、43.75%、6.25%(P>0.05)。 两组突变等位基因-403A频率分别为26.53%和28.13%(P>0.05)。病例组RANTES-28位点C/C、C/G、G/G基因型频率分别为 78.13%、18.75%、3.12%;对照组分别为90.63%、9.37%、0%(P>0.05)。两组突变等位基因-28G频率分别为12.50%和 4.69%(P>0.05)。结论 RANTES-403位点和-28位点SNP与哮喘发病可能没有直接的关系。Objective: To detect the association between the single nucleofide polymorphism (SNPs)of chemokine RANTES in children with asthma. Methods:We use PCR- RFLP to study the SNPs of RANTES polymorphism at - 403 and - 28 sites in the blood specimens of 32 children with asthma and 32 controls. Results:The genotyping frequencies of RANTES - 403 G/G,G/A and A/A in case group were 53.13%, 40.62 % and 6.25 %, respectively; while the genotyping frequencies of RANTES - 403 G/G, G/A and A/A in control were 50,00 %, 43.75 % and 6.25%, respectively( P 〉 0.05) .Them is no significantly difference in the frequency of mutation - 403A allele between case group and controls (26.53% vs 28.13%, P 〉 0.05). The genotyping frequencies of RANTES - 28 C/C, C/G and G/G in case group were 78.13%, 18.75 % and 3.12%, respectively; which were not significantly different from those in controls as 90.63% ,9.37% and 0% ( P 〉 0,05). There is no significantly difference in the frequency of mutation - 28G allele between asthma and controls (12.50 % vs 4.69 %, P 〉 0.05). Conclusions:These results indicate that the SNPs of RANTES promoter are may not associated asthma.
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