McGeachie Michael J, Yates Katherine P, Zhou Xiaobo, Guo Feng, Sternberg Alice L, Van Natta Mark L, Wise Robert A, Szefler Stanley J, Sharma Sunita, Kho Alvin T, Cho Michael H, Croteau-Chonka Damien C, Castaldi Peter J, Jain Gaurav, Sanyal Amartya, Zhan Ye, Lajoie Bryan R, Dekker Job, Stamatoyannopoulos John, Covar Ronina A, Zeiger Robert S, Adkinson N Franklin, Williams Paul V, Kelly H William, Grasemann Hartmut, Vonk Judith M, Koppelman Gerard H, Postma Dirkje S, Raby Benjamin A, Houston Isaac, Lu Quan, Fuhlbrigge Anne L, Tantisira Kelan G, Silverman Edwin K, Tonascia James, Strunk Robert C, Weiss Scott T
1 Channing Division of Network Medicine and.
2 Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Am J Respir Crit Care Med. 2016 Dec 15;194(12):1465-1474. doi: 10.1164/rccm.201602-0250OC.
Patterns of longitudinal lung function growth and decline in childhood asthma have been shown to be important in determining risk for future respiratory ailments including chronic airway obstruction and chronic obstructive pulmonary disease.
To determine the genetic underpinnings of lung function patterns in subjects with childhood asthma.
We performed a genome-wide association study of 581 non-Hispanic white individuals with asthma that were previously classified by patterns of lung function growth and decline (normal growth, normal growth with early decline, reduced growth, and reduced growth with early decline). The strongest association was also measured in two additional cohorts: a small asthma cohort and a large chronic obstructive pulmonary disease metaanalysis cohort. Interaction between the genomic region encompassing the most strongly associated single-nucleotide polymorphism and nearby genes was assessed by two chromosome conformation capture assays.
An intergenic single-nucleotide polymorphism (rs4445257) on chromosome 8 was strongly associated with the normal growth with early decline pattern compared with all other pattern groups (P = 6.7 × 10; odds ratio, 2.8; 95% confidence interval, 2.0-4.0); replication analysis suggested this variant had opposite effects in normal growth with early decline and reduced growth with early decline pattern groups. Chromosome conformation capture experiments indicated a chromatin interaction between rs4445257 and the promoter of the distal CSMD3 gene.
Early decline in lung function after normal growth is associated with a genetic polymorphism that may also protect against early decline in reduced growth groups. Clinical trial registered with www.clinicaltrials.gov (NCT00000575).
儿童哮喘患者肺功能纵向生长和下降模式在决定未来呼吸系统疾病风险(包括慢性气道阻塞和慢性阻塞性肺疾病)方面已显示出重要性。
确定儿童哮喘患者肺功能模式的遗传基础。
我们对581名非西班牙裔白人哮喘患者进行了全基因组关联研究,这些患者先前已根据肺功能生长和下降模式(正常生长、正常生长伴早期下降、生长减缓、生长减缓伴早期下降)进行了分类。在另外两个队列中也测量了最强关联:一个小型哮喘队列和一个大型慢性阻塞性肺疾病荟萃分析队列。通过两种染色体构象捕获试验评估了包含最强烈关联单核苷酸多态性的基因组区域与附近基因之间的相互作用。
与所有其他模式组相比,8号染色体上的一个基因间单核苷酸多态性(rs4445257)与正常生长伴早期下降模式密切相关(P = 6.7×10;优势比,2.8;95%置信区间,2.0 - 4.0);重复分析表明该变体在正常生长伴早期下降和生长减缓伴早期下降模式组中有相反的作用。染色体构象捕获实验表明rs4445257与远端CSMD3基因的启动子之间存在染色质相互作用。
正常生长后肺功能的早期下降与一种遗传多态性相关,该多态性也可能防止生长减缓组的早期下降。在www.clinicaltrials.gov注册的临床试验(NCT00000575)。