Leung Ting Fan, Li Chung Yi, Kong Alice P S, Chan Iris H S, Ng Maggie C Y, Chan Michael H M, So Wing Yee, Wong Gary W K, Lam Christopher W K, Chan Juliana C N
Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.
Pediatr Allergy Immunol. 2009 Sep;20(6):556-62. doi: 10.1111/j.1399-3038.2008.00835.x. Epub 2009 Feb 10.
Airway sensitization requires the expression of prostanoid DP receptor in mice. Recent studies reported that polymorphisms in the gene encoding prostanoid DP receptor (PTGDR) were associated with asthma in White people and Black people, but this association could not be replicated among Latinos and Koreans. This study investigated the association between asthma-related traits and six single nucleotide polymorphisms (SNPs) of PTGDR in Chinese children, consisted of 308 asthmatics and 368 non-allergic controls. Plasma total and aeroallergen-specific immunoglobulin E were measured by immunoassays. PTGDR SNPs were determined by multiplex SNaPshot genotyping. All polymorphic markers followed Hardy-Weinberg equilibrium except G1044A in the controls (p = 0.021). The linkage disequilibrium (LD) scores for these SNPs were moderate to high, and in particular, T-549C and C-441T were in strong LD. Significant interethnic variations in PTGDR alleles and haplotypes (up to 41%) were found in our subjects when compared with White people or Latinos. Asthma diagnosis, atopy and aeroallergen sensitization did not differ among children with different PTGDR genotypes (p > 0.15 for all). Linear regression showed weakly significant associations between T-197C and G1044A of PTGDR and spirometric variables. PTGDR haplotypes were not associated with asthma and atopy phenotypes (p > 0.09 for all). Our results do not support PTGDR to be a major candidate gene for asthma traits in Chinese children.
气道致敏需要小鼠中前列腺素DP受体的表达。最近的研究报道,编码前列腺素DP受体(PTGDR)的基因多态性与白人和黑人的哮喘有关,但这种关联在拉丁裔和韩国人中无法重复。本研究调查了中国儿童中哮喘相关性状与PTGDR的六个单核苷酸多态性(SNP)之间的关联,研究对象包括308名哮喘患者和368名非过敏对照。通过免疫测定法测量血浆总免疫球蛋白E和变应原特异性免疫球蛋白E。通过多重SNaPshot基因分型确定PTGDR SNP。除对照组中的G1044A外(p = 0.021),所有多态性标记均符合哈迪-温伯格平衡。这些SNP的连锁不平衡(LD)分数为中度到高度,特别是T-549C和C-441T处于强LD状态。与白种人或拉丁裔相比,我们的研究对象中PTGDR等位基因和单倍型存在显著的种族间差异(高达41%)。不同PTGDR基因型的儿童在哮喘诊断、特应性和变应原致敏方面没有差异(所有p>0.15)。线性回归显示PTGDR的T-197C和G1044A与肺功能变量之间存在微弱的显著关联。PTGDR单倍型与哮喘和特应性表型无关(所有p>0.09)。我们的结果不支持PTGDR是中国儿童哮喘性状的主要候选基因。