Leung T F, Chan I H S, Wong G W K, Li C Y, Tang N L S, Yung E, Lam C W K
Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.
Clin Exp Allergy. 2007 Oct;37(10):1480-6. doi: 10.1111/j.1365-2222.2007.02799.x.
Asthma is caused by a complex interaction between multiple candidate genes and environmental factors. The Childhood Asthma Management Program reported lung function decline in a significant proportion of Caucasian asthmatic children, but such a relation has not been studied in other populations. Our group recently reported that interleukin-13 (IL13), interleukin-4 receptor-alpha and thymus and the activation-regulated chemokine interacted to influence asthma and raised plasma total IgE. However, there has not been any study that has addressed the genetic influences for longitudinal lung function growth.
We studied the longitudinal changes in spirometric variables in Chinese asthmatic children, and investigated the influence and interactions between eight different loci in six candidate genes as well as environmental factors affecting lung function growth in these children.
Spirometry was performed at baseline and study completion. Genotyping was performed by restriction fragment length polymorphism. Multi-factor dimensionality reduction (MDR) was used to detect any gene-gene or gene-environment interaction.
We prospectively followed 131 Chinese children, aged 9.9 (3.0) years, for 4.5 (0.8) years. Their mean (standard deviation) baseline forced expiratory volume in 1 s (FEV1) was 98.6 (20.6)% of predicted, and FEV1 to forced vital capacity (FVC) ratio was 77.8 (11.3)%. FEV1 and FVC increased by 210 (115) and 248 (148) mL/year during this study, and these changes were significantly larger among males (P<0.0001). Univariate analysis revealed a significant association between annual FEV1 change and C1570T of signal transducer and activator of transcription 6 gene (STAT6; P=0.009). Linear regression confirmed this finding (P=0.041). Using MDR, we detected a significant 3-locus interaction between IL13 R130Q, ADRB2 R16G and STAT6 C1570T for determining change in FVC (P=0.045).
Our data suggest that STAT6 may influence lung function growth in asthmatic children. We also found significant interactions among several atopy-related genetic polymorphisms for influencing FVC change.
哮喘是由多个候选基因与环境因素之间复杂的相互作用引起的。儿童哮喘管理项目报告称,相当一部分白种人哮喘儿童的肺功能出现下降,但尚未在其他人群中研究这种关系。我们的研究小组最近报告称,白细胞介素 - 13(IL13)、白细胞介素 - 4受体 - α以及胸腺和激活调节趋化因子相互作用影响哮喘并使血浆总IgE升高。然而,尚未有任何研究探讨基因对肺功能纵向生长的影响。
我们研究了中国哮喘儿童肺功能指标的纵向变化,并调查了六个候选基因中八个不同位点之间的相互影响以及环境因素对这些儿童肺功能生长的影响。
在基线和研究结束时进行肺功能测定。通过限制性片段长度多态性进行基因分型。使用多因素降维法(MDR)检测基因 - 基因或基因 - 环境相互作用。
我们前瞻性地跟踪了131名9.9(3.0)岁的中国儿童,为期4.5(0.8)年。他们1秒用力呼气量(FEV1)的平均(标准差)基线值为预测值的98.6(20.6)%,FEV1与用力肺活量(FVC)的比值为77.8(11.3)%。在本研究期间,FEV1和FVC每年分别增加210(115)和248(148)mL,男性的这些变化明显更大(P<0.0001)。单因素分析显示,每年FEV1变化与信号转导和转录激活因子6基因(STAT6)的C1570T之间存在显著关联(P = 0.009)。线性回归证实了这一发现(P = 0.041)。使用MDR,我们检测到IL13 R130Q、ADRB2 R16G和STAT6 C1570T之间存在显著的三位点相互作用,可决定FVC的变化(P = 0.045)。
我们的数据表明,STAT6可能影响哮喘儿童的肺功能生长。我们还发现,几种与特应性相关的基因多态性之间存在显著的相互作用,可影响FVC的变化。