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带有北非血统影响的南欧人群哮喘的混合映射分析。

Admixture mapping of asthma in southwestern Europeans with North African ancestry influences.

机构信息

Research Unit, Hospital Universitario Nuestra Señora de Candelaria, Universidad de La Laguna, Santa Cruz de Tenerife, Spain.

Research Unit, Hospital Universitario de Gran Canaria Doctor Negrín, Las Palmas de Gran Canaria, Spain.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2020 May 1;318(5):L965-L975. doi: 10.1152/ajplung.00344.2019. Epub 2020 Mar 18.

DOI:10.1152/ajplung.00344.2019
PMID:32186396
Abstract

The prevalence of asthma symptoms in Canary Islanders, a southwestern European population from Spain, is almost three times higher than the country average. Because the genetic risks identified so far explain <5% of asthma heritability, here we aimed to discover new asthma loci by completing the first admixture mapping study in Canary Islanders leveraging their distinctive genetic makeup, where significant northwest African influences coexist in the European genetic diversity landscape. A 2-stage study was conducted in 1,491 unrelated individuals self-declaring having a Canary Islands origin for the 4 grandparents. Local ancestry estimates were obtained for the shared positions with reference data from putative ancestral populations from Europe, North Africa, and sub-Saharan Africa. Case-control deviations in local ancestry were tested for each ancestry separately using logistic regressions adjusted for principal components, followed by fine-mapping analyses based on imputed genotypes and analyses of the likely deleterious exonic variants. The admixture mapping analysis of asthma detected that local North African ancestry in a locus spanning 365 kb of chromosome 16q23.3 was associated with asthma risk at study-wide significance [lowest = 1.12 × 10; odds ratio (OR) = 2.05; 95% confidence interval (CI) = 1.41-3.00]. Fine-mapping studies identified a variant associated with asthma, and results were replicated in independent samples (rs3852738, OR = 1.34; 95% CI = 1.13-1.59, = 7.58 × 10). Whole exome sequencing data from a subset of individuals revealed an enrichment of likely deleterious variants among asthma cases in 16q23.3, particularly in the phospholipase Cγ2 () gene ( = 3.67 × 10). By completing the first mapping study of asthma in admixed populations from Europe, our results revealed a new plausible asthma locus.

摘要

加那利群岛居民(西班牙西南部的欧洲人群)的哮喘症状流行率几乎是该国平均水平的三倍。由于迄今为止确定的遗传风险仅能解释哮喘遗传率的<5%,因此我们旨在通过完成加那利群岛居民的首次混合人群的定位研究来发现新的哮喘基因座,因为在欧洲遗传多样性景观中,其独特的遗传构成存在显著的西北非影响。在 1491 名无亲缘关系的个体中进行了 2 阶段研究,这些个体自我宣称其 4 位祖辈来自加那利群岛。对于与来自欧洲、北非和撒哈拉以南非洲的假定祖先群体的参考数据共享的位置,获得了本地祖先的估计值。使用逻辑回归分别针对每个祖先对本地祖先的病例对照偏差进行了测试,该回归模型针对主成分进行了调整,然后基于已导入的基因型进行了精细映射分析,并对可能有害的外显子变异进行了分析。对哮喘的混合映射分析检测到,跨越染色体 16q23.3 365 kb 的一个位点上的本地北非祖源与研究范围内的哮喘风险相关(最低值为 1.12×10;比值比[OR]为 2.05;95%置信区间[CI]为 1.41-3.00])。精细映射研究确定了与哮喘相关的一个变体,并且在独立样本中得到了复制(rs3852738,OR=1.34;95%CI=1.13-1.59, = 7.58×10)。从个体的子集获得的外显子组测序数据显示,在 16q23.3 中,哮喘病例中存在可能有害的变体富集,尤其是在磷脂酶 Cγ2()基因中( = 3.67×10)。通过完成欧洲混合人群的哮喘首次映射研究,我们的结果揭示了一个新的可能的哮喘基因座。

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