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首页> 外文期刊>Human Molecular Genetics >Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
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Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.

机译:全基因组连锁分析严重,早发的慢性阻塞性肺疾病:气流阻塞和慢性支气管炎表型。

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摘要

Familial aggregation of chronic obstructive pulmonary disease (COPD) has been demonstrated, but linkage analysis of COPD-related phenotypes has not been reported previously. An autosomal 10 cM genome-wide scan of short tandem repeat (STR) polymorphic markers was analyzed for linkage to COPD-related phenotypes in 585 members of 72 pedigrees ascertained through severe, early-onset COPD probands without severe alpha1-antitrypsin deficiency. Multipoint non-parametric linkage analysis (using the ALLEGRO program) was performed for qualitative phenotypes including moderate airflow obstruction [forced expiratory volume at one second (FEV(1)) < 60% predicted, FEV(1)/FVC < 90% predicted], mild airflow obstruction (FEV(1) < 80% predicted, FEV(1)/FVC < 90% predicted) and chronic bronchitis. The strongest evidence for linkage in all subjects was observed at chromosomes 12 (LOD = 1.70) and 19 (LOD = 1.54) for moderate airflow obstruction, chromosomes 8 (LOD = 1.36) and 19 (LOD = 1.09) for mild airflow obstruction and chromosomes 19 (LOD = 1.21) and 22 (LOD = 1.37) for chronic bronchitis. Restricting analysis to cigarette smokers only provided increased evidence for linkage of mild airflow obstruction and chronic bronchitis to several genomic regions; for mild airflow obstruction in smokers only, the maximum LOD was 1.64 at chromosome 19, whereas for chronic bronchitis in smokers only, the maximum LOD was 2.08 at chromosome 22. On chromosome 12p, 12 additional STR markers were genotyped, which provided additional support for an airflow obstruction locus in that region with a non-parametric multipoint approach for moderate airflow obstruction (LOD = 2.13) and mild airflow obstruction (LOD = 1.43). Using a dominant model with the STR markers on 12p, two point parametric linkage analysis of all subjects demonstrated a maximum LOD score of 2.09 for moderate airflow obstruction and 2.61 for mild airflow obstruction. In smokers only, the maximum two point LOD score for mild airflow obstruction was 3.14. These observations provide suggestive evidence that there is a locus on chromosome 12p which contributes to susceptibility to early-onset COPD.
机译:慢性阻塞性肺疾病(COPD)的家族聚集已得到证明,但以前尚未报道COPD相关表型的连锁分析。短串联重复序列(STR)多态性标记的常染色体10 cM全基因组扫描分析了72个家谱中的585个成员与COPD相关表型的连锁关系,这些成员是通过严重,早发的COPD先证者确定的,没有严重的α1-抗胰蛋白酶缺乏症。对定性表型进行了多点非参数连锁分析(使用ALLEGRO程序),包括中等气流阻塞[一秒钟的呼气量(FEV(1))<预测的60%,FEV(1)/ FVC <预测的90%] ,轻度气流阻塞(预测的FEV(1)<80%,预测的FEV(1)/ FVC <90%)和慢性支气管炎。在中度气流阻塞的第12号染色体(LOD = 1.70)和19(LOD = 1.54)处观察到所有受试者连锁的最有力证据,在轻度气流障碍和染色体上第8号染色体(LOD = 1.36)和19(LOD = 1.09)被观察到。慢性支气管炎为19(LOD = 1.21)和22(LOD = 1.37)。仅对吸烟者进行的分析仅提供了增加的证据,表明轻度气流阻塞和慢性支气管炎与几个基因组区域相关。仅针对吸烟者的轻度气流阻塞,在19号染色体上的最大LOD为1.64,而仅对于吸烟者的慢性支气管炎,在22号染色体上的最大LOD为2.08。在12p染色体上,对12个另外的STR标记进行了基因分型,从而为该区域的气流阻塞点,采用非参数多点方法进行中度气流阻塞(LOD = 2.13)和轻度气流阻塞(LOD = 1.43)。使用在12p上带有STR标记的显性模型,对所有受试者的两点参数连锁分析显示,中等气流障碍的最大LOD得分为2.09,轻度气流障碍的最大LOD得分为2.61。仅在吸烟者中,轻度气流阻塞的最高两点LOD得分为3.14。这些观察结果提供了暗示性证据,表明在12p染色体上有一个基因座,该基因座易患早发性COPD。

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