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欧洲人β防御素基因的拷贝数变异:与肺功能、慢性阻塞性肺疾病或哮喘无关的证据不足。

Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma.

机构信息

Department of Health Sciences, University of Leicester, Leicester, United Kingdom.

Department of Genetics, University of Leicester, Leicester, United Kingdom.

出版信息

PLoS One. 2014 Jan 3;9(1):e84192. doi: 10.1371/journal.pone.0084192. eCollection 2014.

Abstract

Lung function measures are heritable, predict mortality and are relevant in diagnosis of chronic obstructive pulmonary disease (COPD). COPD and asthma are diseases of the airways with major public health impacts and each have a heritable component. Genome-wide association studies of SNPs have revealed novel genetic associations with both diseases but only account for a small proportion of the heritability. Complex copy number variation may account for some of the missing heritability. A well-characterised genomic region of complex copy number variation contains beta-defensin genes (DEFB103, DEFB104 and DEFB4), which have a role in the innate immune response. Previous studies have implicated these and related genes as being associated with asthma or COPD. We hypothesised that copy number variation of these genes may play a role in lung function in the general population and in COPD and asthma risk. We undertook copy number typing of this locus in 1149 adult and 689 children using a paralogue ratio test and investigated association with COPD, asthma and lung function. Replication of findings was assessed in a larger independent sample of COPD cases and smoking controls. We found evidence for an association of beta-defensin copy number with COPD in the adult cohort (OR = 1.4, 95%CI:1.02-1.92, P = 0.039) but this finding, and findings from a previous study, were not replicated in a larger follow-up sample(OR = 0.89, 95%CI:0.72-1.07, P = 0.217). No robust evidence of association with asthma in children was observed. We found no evidence for association between beta-defensin copy number and lung function in the general populations. Our findings suggest that previous reports of association of beta-defensin copy number with COPD should be viewed with caution. Suboptimal measurement of copy number can lead to spurious associations. Further beta-defensin copy number measurement in larger sample sizes of COPD cases and children with asthma are needed.

摘要

肺功能测量具有遗传性,可预测死亡率,并且与慢性阻塞性肺疾病(COPD)的诊断相关。COPD 和哮喘是气道疾病,对公众健康有重大影响,并且每个疾病都有遗传成分。对 SNP 的全基因组关联研究揭示了与这两种疾病相关的新的遗传关联,但仅占遗传的一小部分。复杂的拷贝数变异可能解释了一些缺失的遗传。一个特征良好的复杂拷贝数变异基因组区域包含β-防御素基因(DEFB103、DEFB104 和 DEFB4),它们在先天免疫反应中起作用。先前的研究表明这些和相关基因与哮喘或 COPD 有关。我们假设这些基因的拷贝数变异可能在一般人群的肺功能以及 COPD 和哮喘风险中发挥作用。我们使用等位基因比率测试对 1149 名成人和 689 名儿童进行了该基因座的拷贝数分型,并研究了其与 COPD、哮喘和肺功能的关联。在更大的 COPD 病例和吸烟对照的独立样本中评估了发现的复制情况。我们发现,β-防御素拷贝数与成人队列中的 COPD 存在关联(OR=1.4,95%CI:1.02-1.92,P=0.039),但这一发现和之前的一项研究结果,在更大的随访样本中没有得到复制(OR=0.89,95%CI:0.72-1.07,P=0.217)。在儿童中,没有发现与哮喘存在关联的有力证据。我们没有发现β-防御素拷贝数与一般人群肺功能之间存在关联的证据。我们的研究结果表明,以前关于β-防御素拷贝数与 COPD 关联的报告应谨慎看待。拷贝数测量不理想可能导致虚假关联。需要在更大的 COPD 病例和哮喘儿童样本中进一步进行β-防御素拷贝数测量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908b/3880289/684f418589f7/pone.0084192.g001.jpg

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