首页> 外文期刊>The Journal of Allergy and Clinical Immunology >The PTGDR gene is not associated with asthma in 3 ethnically diverse populations.
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The PTGDR gene is not associated with asthma in 3 ethnically diverse populations.

机译:在3个种族不同的人群中,PTGDR基因与哮喘无关。

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BACKGROUND: The prostanoid DP receptor (PTGDR) gene on chromosome 14q22.1 has been identified as an asthma susceptibility gene. A haplotype with decreased transcription factor binding and transcription efficiency was associated with decreased asthma susceptibility in African American and white subjects. The significance of PTGDR gene variants in asthma has yet to be determined in Latinos, the largest US minority population, nor has the association been replicated in other populations. OBJECTIVE: To determine the role of PTGDR gene variants in asthma susceptibility and asthma-related traits among the Mexican, Puerto Rican, and African American populations. METHODS: We determined whether single nucleotide polymorphisms (SNPs) and haplotypes in PTGDR were associated with asthma and asthma-related traits by family-based and cross-sectional cohort analyses in 336 Puerto Rican and 273 Mexican asthmatic trios and by case-control analysis among African American subjects with asthma and healthy controls (n = 352). RESULTS: We identified 13 SNPs in the PTGDR gene, and 6 were further analyzed. There was no significant association between PTGDR variants and asthma by family-based or case-control analyses. SNPs -441C and -197C and haplotype TTT showed marginal association with asthma-related traits in Mexican subjects. SNP -441 genotype TT (P = .05) and haplotype TTT (P = .02) were associated with increased IgE levels in African Americans. CONCLUSION: We conclude that the PTGDR gene is not a significant risk factor for asthma among Puerto Ricans, Mexicans, or African Americans. CLINICAL IMPLICATIONS: Asthma candidate genes provide insights to pathophysiology and potentially new therapeutic targets, although the PTGDR gene was not found to be a significant risk factor for asthma in 3 populations.
机译:背景:14q22.1染色体上的前列腺素DP受体(PTGDR)基因已被鉴定为哮喘易感基因。在非洲裔美国人和白人受试者中,转录因子结合和转录效率降低的单倍型与哮喘易感性降低相关。 PTGDR基因变异在哮喘中的重要性尚未在美国最大的少数族裔拉丁美洲人中确定,也未在其他人群中复制。目的:确定PTGDR基因变异在墨西哥人,波多黎各人和非裔美国人人群中的哮喘易感性和哮喘相关性状中的作用。方法:我们通过对336名波多黎各人和273名墨西哥哮喘三重症患者进行家庭和横断面队列分析,并通过病例对照分析,确定了PTGDR中的单核苷酸多态性(SNPs)和单倍型是否与哮喘和与哮喘相关的特征相关患有哮喘和健康对照的非裔美国人受试者(n = 352)。结果:我们在PTGDR基因中鉴定出13个SNP,并进一步分析了6个。通过基于家庭或病例对照的分析,PTGDR变异与哮喘之间无显着关联。 SNPs -441C和-197C以及单倍型TTT在墨西哥受试者中显示与哮喘相关性状的边缘关联。 SNP -441基因型TT(P = .05)和单倍型TTT(P = .02)与非洲裔美国人的IgE水平升高相关。结论:我们得出结论,在波多黎各人,墨西哥人或非裔美国人中,PTGDR基因不是哮喘的重要危险因素。临床意义:哮喘候选基因为病理生理学和潜在的新治疗靶点提供了见识,尽管未发现PTGDR基因在3个人群中是哮喘的重要危险因素。

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