Xu Tianyi, Shi Yiru, Liu Jiangbo, Liu Yun, Zhu Ailin, Xie Cui, Zhang Yan, Chen Yan, Ren Lirong
1 Department of Obstetrics, International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
2 Department of Dermatology, Bao'an Maternal and Child Health Hospital, Shenzhen, Guangdong, China.
J Int Med Res. 2018 Jan;46(1):115-121. doi: 10.1177/0300060517714934. Epub 2017 Jul 21.
Objective The rs10229583 polymorphism near paired box gene 4 ( PAX4) is associated with insulin resistance and type 2 diabetes. Mutations in the PAX4 gene may be associated with impaired differentiation/development of pancreatic islet beta cells during fetal development and, consequently, a compromised insulin response to high blood glucose. To ascertain whether this polymorphism plays a role in gestational diabetes mellitus (GDM), we investigated the genotypic and allele frequency differences between GDM and normal pregnancies. Methods A total of 310 GDM and 440 normal pregnancies were evaluated. Allele and genotype frequencies of rs10229583 were determined for all participants with Sanger sequencing and SNaPshot. Association of the allele and genotypes of the single nucleotide polymorphism with the disease was analyzed using Pearson's χ test and OR (odds ratio). Results The G allele was more frequent in patients with GDM compared with controls (OR = 1.47, 95% confidence interval (CI): 1.12-1.939). The GG genotype frequency of rs10229583 was significantly different between subjects with GDM and normal controls (OR = 1.411, 95% CI: 1.032-1.928). The OR of the GA + GG genotype was 3.182 (95% CI: 1.294-7.826) for patients with GDM compared with controls. Conclusion The present study suggests that rs10229583 is associated with GDM.
配对盒基因4(PAX4)附近的rs10229583多态性与胰岛素抵抗及2型糖尿病相关。PAX4基因突变可能与胎儿发育期间胰岛β细胞分化/发育受损有关,进而导致胰岛素对高血糖的反应受损。为确定该多态性是否在妊娠期糖尿病(GDM)中起作用,我们调查了GDM患者与正常妊娠者之间的基因型和等位基因频率差异。方法:共评估了310例GDM患者和440例正常妊娠者。采用桑格测序法和SNaPshot法测定所有参与者rs10229583的等位基因和基因型频率。使用Pearson卡方检验和OR(优势比)分析单核苷酸多态性的等位基因和基因型与疾病的关联。结果:与对照组相比,GDM患者中G等位基因更为常见(OR = 1.47,95%置信区间(CI):1.12 - 1.939)。rs10229583的GG基因型频率在GDM患者和正常对照组之间存在显著差异(OR = 1.411,95% CI:1.032 - 1.928)。与对照组相比,GDM患者中GA + GG基因型的OR为3.182(95% CI:1.294 - 7.826)。结论:本研究表明rs10229583与GDM相关。