摘要
目的研究促酰化蛋白(acylation-stimulating protein,ASP)的功能受体C5L2基因的SNP位点C698T多态性与中山地区人群妊娠期糖尿病(GDM)的相关性。方法本研究采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对来自2012年2013年中山博爱医院共285例孕妇检测C5L2基因多态性,评估其与GDM的相关性。其中GDM组174例,血糖正常103例设为对照组。GDM组和对照组基因型分布运用logistic回归模型分析。GDM组相关表型运用多重回归模型分析。结果C5L2基因C698T杂合子基因型在GDM组和对照组的分布频率分别为0.6%和1.9%,差异不具有统计学意义(校正χ2=0.213,P=0.6>0.05)。基因型TT在GDM组和对照组均未发现。结论在中山地区人群中,C5L2基因C698T基因多态性与GDM的发生可能不具有相关性。
Objective: This study aimed to examine possible genetic effects of C5L2 gene polymorphisms (C698T) on the risk of GDM of Zhongshan city population. Methods: C5L2 gene 698C〉T variant from 185 patients with GDM and 100 healthy as control subjects was detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The genotype distributions between GDM and controls were analyzed using logistic regression models. In addition, GDM-related phenotypes were analyzed using multiple regression models. Result: Heterozygote carders of the C698T genotype were no different between GDM and controls (X2=0.213, P=0.644〉0.05) . We have not found TT genotype in GDM or control. Conclusion: The CT genotype of C5L2 gene might not be a risk factor of GDM in Zhongshan population.
出处
《中国优生与遗传杂志》
2014年第9期16-18,共3页
Chinese Journal of Birth Health & Heredity
基金
广东省医学科研项目(A2011756)
中山市科技局资助项目(20113A017)