|
|
Correlation Between PTPN22 Gene Polymorphism and Susceptibility of Idiopathic Thrombocytopenic Purpura in Children |
LI Fang-fang, LI Tian-yu, XU Da-ming,et al |
Hematology Department,Wu xi People‘s Hospital,Jiang su 214000 China |
|
|
Abstract Objective To analyze the correlation between non-receptor protein tyrosine phosphatase 22 (PTPN22) gene polymorphism and the susceptibility of idiopathic thrombocytopenic purpura (ITP) in children. Methods Gene polymorphism of PTPN22-1123G>C (rs2488457) in 120 children with ITP (the observation group) and 80 normal children (the control group) was determined by PCR-MALDI-TOF MS method. Results The C frequency of PTPN22-1123G > C allele in the observation group was 62.50% ,which was significantly lower than that in the control group (71.25%) (P<0.05), while there were no significant differences in genotypes between the two groups (P>0.05). The allele frequency showed significant differences in boys in the two groups (P<0.05), while there were no significant differences in girls (P>0.05). There were no significant differences in genotypes in children with the same gender (P>0.05). Conclusion The PTPN22-1123G>C polymorphism is associated with susceptibility of ITP in children. C is the dominant allele while G is the risk allele. The allele frequencies of PTPN22-1123G > C may be related to the gender of children.
|
|
|
|
|
|
[1] 郭力,马道新,侯明,等.国际工作组免疫性血小板减少新分期标准与糖皮质激素疗效的关系[J].中华内科杂志,2010,49(12):1020-1023. [2] 李晓红,盛光耀.特发性血小板减少性紫癜患儿HLA-DRB1基因多态性[J].郑州大学学报(医学版),2011,46(1):97-99. [3] 张春来,陈晓建,闫晓华,等.TRAIL基因多态性与特发性血小板减少性紫癜的相关性研究[J].山东医药,2012,52(20):38-41. [4] 张之南,沈悌.血液病诊断及疗效标准[M].第3版. 北京: 出版社,2007: 172-176. [5] 冯尽意,张立新.血清sHLA-G在慢性特发性血小板减少性紫癜患者中的表达及意义[J].医学临床研究,2016,33(4):745-747. [6] 何丽雅,黄钰君,赖冬波,等.FCGR2B基因多态性与儿童特发性血小板减少性紫癜易感性的相关性研究[J].中国实验血液学杂志,2009,17(3):729-733.
|
|
|
|