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遗传因素在儿童早期对环境过敏原致敏的发展中的作用。

Genetic determinants in the development of sensitization to environmental allergens in early childhood.

机构信息

Division of Allergy and Clinical Immunology, Johns Hopkins University School of Medicine Baltimore, Maryland, 21224.

Center on Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Johns Hopkins University Bloomberg School of Public Health Baltimore, Maryland, 21205.

出版信息

Immun Inflamm Dis. 2014 Nov;2(3):193-204. doi: 10.1002/iid3.38. Epub 2014 Nov 20.

Abstract

Sensitization to environmental allergens remains one of the strongest risk factors for asthma, and there is likely a genetic basis. We sought to identify genetic determinants for the development of allergic sensitization to environmental allergens, particularly cockroach allergen, in early childhood. A total of 631 children with the information about genotypic data on 895 single nucleotide polymorphisms (SNPs) in 179 candidate genes were selected from an existing dataset (Boston Birth Cohort). Genetic analysis was performed for allergic sensitizations among all subjects and sub-population, Black/African, respectively. Eight SNPs in seven genes showed significant association with allergic sensitization with P < 0.05, including two top SNPs, rs7851969 in JAK2 (P = 0.003) and rs11739089 in CNOT6 (P = 0.008). When analyses were specifically performed for cockroach sensitization, 16 SNPs in 13 genes showed P < 0.05, including five genes with SNPs at P < 0.01 (JAK1, JAK3, IL5RA, FCER1A, and ADAM33). Particularly, haplotype analyses demonstrated that multiple-haplotypes in FCER1A were significantly associated with cockroach sensitization with the strongest association for a 2-marker haplotype (rs6665683T-rs12136904T, P = 0.001). Furthermore, SNP rs6665683 was marginally associated with the levels of cockroach allergen specific IgE. When a similar analysis was performed for house dust mite, four SNPs in three genes (JAK2, MAML1, and NOD1) had P < 0.01. Of these, JAK2 appeared to be an only gene showing association across the sensitizations we analyzed. Some of findings were further validated when analysis was limited to black population. Our study identified several loci that may confer the susceptibility to allergic sensitization, and suggested that sensitization to allergens may depend on their unique loci.

摘要

对环境过敏原的致敏仍然是哮喘的最强危险因素之一,并且可能存在遗传基础。我们试图确定导致儿童早期对环境过敏原(尤其是蟑螂过敏原)过敏致敏的遗传决定因素。从现有数据集(波士顿出生队列)中选择了 631 名儿童,他们具有有关 179 个候选基因中 895 个单核苷酸多态性(SNP)的基因型数据的信息。对所有受试者和亚人群(黑人和非洲裔)进行了过敏致敏的遗传分析。在七个基因中的八个 SNP 与过敏致敏相关,P 值均小于 0.05,包括两个顶级 SNP,JAK2 中的 rs7851969(P=0.003)和 CNOT6 中的 rs11739089(P=0.008)。当专门针对蟑螂致敏进行分析时,在 13 个基因中有 16 个 SNP 显示 P 值小于 0.05,其中五个基因的 SNP 值小于 0.01(JAK1、JAK3、IL5RA、FCER1A 和 ADAM33)。特别是,单体型分析表明,FCER1A 中的多个单体型与蟑螂致敏显著相关,最强的关联是 2 个标记单体型(rs6665683T-rs12136904T,P=0.001)。此外,SNP rs6665683 与蟑螂过敏原特异性 IgE 水平呈边际相关。当对屋尘螨进行类似分析时,三个基因(JAK2、MAML1 和 NOD1)中的四个 SNP 具有 P 值小于 0.01。其中,JAK2 似乎是我们分析的过敏致敏中唯一具有关联的基因。当分析仅限于黑人时,其中一些发现得到了进一步验证。我们的研究确定了几个可能赋予过敏致敏易感性的基因座,并表明对过敏原的致敏可能取决于其独特的基因座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ba7/4257764/584bfa107cde/iid30002-0193-f1.jpg

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