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Has-mir-146a rs2910164多态性与免疫性血小板减少症风险

Has-mir-146a rs2910164 polymorphism and risk of immune thrombocytopenia.

作者信息

Zhao Haifeng, Zhang Yizhuo, Xue Feng, Xu Jianfen, Fang Zhi

机构信息

Department of Hematology and Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy , Tianjin , PR China .

出版信息

Autoimmunity. 2014 May;47(3):173-6. doi: 10.3109/08916934.2014.883503. Epub 2014 Feb 6.

Abstract

The purpose of this study was to determine the association of single nucleotide polymorphisms (SNP) of the has-mir-146a (miR-146a) genes with the risk for immune thrombocytopenia (ITP). The genotyping of miR-146a rs2910164 polymorphism was detected by polymerase chain reaction-restriction fragment length polymorphism. In the patients with ITP, the frequencies of GG, GC and CC genotypes and G and C alleles were 12.5%, 47.9%, 39.6%, 36.4% and 63.6%, respectively. There was no significant difference in genotype and alleles distribution between the ITP patient and the controls (p = 0.77 and 0.51, respectively). No significant differences were found between the two groups when stratified by the age and disease course including acute adult, chronic adult, acute childhood and chronic childhood. In conclusion, there was no association between the SNP of miR-146a and the susceptibility to ITP in a Chinese population.

摘要

本研究旨在确定has-mir-146a(miR-146a)基因的单核苷酸多态性(SNP)与免疫性血小板减少症(ITP)风险之间的关联。采用聚合酶链反应-限制性片段长度多态性方法检测miR-146a rs2910164多态性的基因分型。在ITP患者中,GG、GC和CC基因型以及G和C等位基因的频率分别为12.5%、47.9%、39.6%、36.4%和63.6%。ITP患者与对照组之间的基因型和等位基因分布无显著差异(p分别为0.77和0.51)。按年龄和病程分层(包括急性成人、慢性成人、急性儿童和慢性儿童)后,两组之间未发现显著差异。总之,在中国人群中,miR-146a的SNP与ITP易感性之间无关联。

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