Yiallouros Panayiotis K, Kouis Panayiotis, Kolokotroni Ourania, Youhanna Sonia, Savva Savvas C, Dima Kleanthi, Zerva Aikaterini, Platt Danielle, Middleton Nicos, Zalloua Pierre
Medical School, University of Cyprus, Nicosia, Cyprus.
Cyprus International Institute for Environmental & Public Health in Association with Harvard School of Public Health, Cyprus University of Technology, Limassol, Cyprus.
Ital J Pediatr. 2016 Jul 13;42(1):67. doi: 10.1186/s13052-016-0276-1.
In a cohort of children in Cyprus, we recently reported low levels of high density lipoprotein cholesterol (HDL-C) to be associated with asthma. We examined whether genetic polymorphisms that were previously linked individually to asthma, obesity, or HDL-C are associated with both asthma and HDL-C levels in the Cyprus cohort.
We assessed genotypes frequencies in current-wheezers (n = 190) and non-asthmatic controls (n = 671) and HDL-C levels across several genotypes. Binary logistic regression models were used to assess the effect of genotypes on wheezing risk and examined whether this effect is carried out through changes of HDL-C.
Of the 16 polymorphisms tested, two polymorphisms TNFa rs3093664 and PRKCA rs9892651 presented significant differences in genotype distribution among current-wheezers and controls. Higher HDL-C levels were noted in carriers of genotype GG of polymorphism TNFa rs3093664 that was protective for wheezing Vs AG and AA genotypes (65.3 Vs 51.8 and 53.3 mg/dl, p-value < 0.001 and p-value for trend = 0.028). In polymorphism PRKCA rs9892651, HDL-C levels were lower in carriers of CC and TC genotypes that were more frequent in current-wheezers Vs TT genotype (52.2 and 52.7 Vs 55.2 mg/dl, p-value = 0.042 and p-value for trend = 0.02). The association of TNFa rs3093664 with wheezing is partly mediated by its effect on HDL-C whereas association of PRKCA rs9892651 with wheezing appeared to be independent of HDL-C.
We found evidence that two SNPs located in different genetic loci, are associated with both wheezing and HDL-C levels, although more studies in other populations are needed to confirm our results.
在塞浦路斯的一组儿童中,我们最近报告高密度脂蛋白胆固醇(HDL-C)水平低与哮喘有关。我们研究了先前分别与哮喘、肥胖或HDL-C相关的基因多态性是否与塞浦路斯队列中的哮喘和HDL-C水平都有关。
我们评估了当前喘息者(n = 190)和非哮喘对照组(n = 671)的基因型频率以及几种基因型的HDL-C水平。使用二元逻辑回归模型评估基因型对喘息风险的影响,并检查这种影响是否通过HDL-C的变化来实现。
在测试的16种多态性中,两种多态性TNFa rs3093664和PRKCA rs9892651在当前喘息者和对照组的基因型分布上存在显著差异。对于多态性TNFa rs3093664,GG基因型携带者的HDL-C水平较高,该基因型对喘息有保护作用,而AG和AA基因型则较低(65.3对51.8和53.3mg/dl,p值<0.001,趋势p值 = 0.028)。在多态性PRKCA rs9892651中,CC和TC基因型携带者的HDL-C水平较低,这两种基因型在当前喘息者中更常见,而TT基因型则较高(52.2和52.7对55.2mg/dl,p值 = 0.042,趋势p值 = 0.02)。TNFa rs3093664与喘息的关联部分由其对HDL-C的影响介导,而PRKCA rs9892651与喘息的关联似乎独立于HDL-C。
我们发现有证据表明位于不同基因位点的两个单核苷酸多态性与喘息和HDL-C水平都有关,尽管需要在其他人群中进行更多研究来证实我们的结果。