期刊文献+

miR-137基因多态性与中国南方人群精神分裂症的关联性研究 被引量:1

Association of miRNA-137 polymorphism with schizophrenia in a southern Chinese Han population
下载PDF
导出
摘要 目的采用中国南方汉族人群样本对miR-137基因多态性与精神分裂症的相关性进行研究。方法收集944例精神分裂症患者(精神分裂症组)及938例健康对照者(对照组)外周血液,采用SnaPshot技术对rs1625579位点进行基因分型,比较该位点等位基因频率分布在精神分裂症组和对照组,以及在精神分裂症患者临床变量分组中的差异。结果在精神分裂症组和对照组中基因型分布差异有统计学意义(x2=4.426,P=0.035),等位基因分布差异有统计学意义(x2=4.813,P=0.028)。按性别分组后,女性精神分裂患者和对照组之间基因型分布差异有统计学意义(x2=3.928,P=0.047),等位基因分布差异有统计学意义(x2=3.957,P=0.047)。结论研究结果证实了miR-137基因多态性与精神分裂症的相关性,同时发现了miR-137在精神分裂症发病调控过程中的性别特异性。 Objective To assay the association between miR-137 gene polymorphism and schizophrenia in a southern Chinese Han population. Methods We genotyped 944 schizophrenic patients and 938 controls for the risk single nucleotide polymorphism (SNP) rs1625579 by the SnaPshot technique and compared the clinical profiles and neurocognitive functions of different genotypes. Results Both the genotype and allele distributions of the rs1625579 SNP were significantly different between patients and controls (X2 = 4. 426, P = 0. 035 ; X2 = 4.813, P = 0. 028). Gender-stratified analysis revealed the significant difference in genotype and allele distributions in female patients(X2= 3. 928,P=0. 047;X2 = 3. 957, P= 0. 047). Conclusion The results of our study verifies that miR-137 gene polymorphism is associated with schizophrenia. It is discovered that miR-137 has the gender specificity in the regulation process of schizophrenia pathogenesis.
出处 《重庆医学》 CAS 北大核心 2016年第13期1733-1735,1739,共4页 Chongqing medicine
基金 国家自然科学基金资助项目(31171219)
关键词 多态现象 遗传 基因 精神分裂症 miR-137 rs1625579多态性 汉族 polymorphism, genetic genes schizophrenia miR-137 rsl 625579 polymorphism Han nationality
  • 相关文献

参考文献24

  • 1Allen NC,Bagade S, Mcqueen MB, et al. Systematic metaanalyses and field synopsis of genetic association studies in schizophrenia: the SzGene database [J]. Nat Genet, 2008,40(7):827-834. 被引量:1
  • 2Cannon TD. Abnormalities of brain structure and function in schizophrenia: implications for aetiology and pathophysiology[J]. Ann Med, 1996,28 (6) : 533-539. 被引量:1
  • 3Murchison EP, Partridge JF, Tam OH, et al. Characterization of dicer-deficient murine embryonic stem cells[J]. Proc Natl Acad Sci U S A,2005,102(34):12135-12140. 被引量:1
  • 4Wang Y, Medvid R, Melton C, et al. DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal[J]. Nat Genet, 2007,39 (3) : 380-385. 被引量:1
  • 5Stark KL, Xu B,Bagchi A, et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11- deletion mouse model[J]. Nat Genet, 2008,40 (6) :751- 760. 被引量:1
  • 6Sewell RA, Perry EB, Karper LP, et al. Clinical significance of neurological soft signs in schizophrenia:factor analysis of the Neurological Evaluation Scale[J]. Schizophr Res, 2010,124(1/3) : 1-12. 被引量:1
  • 7Skaper SD. Neuronal growth-promoting and inhibitory cues in neuroprotection and neuroregeneration[J].Methods Mol Biol,2012,846:13-22. 被引量:1
  • 8Yang Y,Calakos N. Presynaptic long-term plasticity[J], Front synaptic neurosci, 2013,5 : 8. 被引量:1
  • 9Du J,Fu C,Sretavan DW. Eph/ephrin signaling as a potential therapeutic target after central nervous system injury[J]. Curr Pharm Des, 2007,13 (24) : 2507-2518. 被引量:1
  • 10Nikolov DB, Xu K, Himanen JP. Eph/ephrin recognition and the role of Eph/ephrin clusters in signaling initiation [J].Biochim Biophys Acta, 2013,1834(10) :2160-2165. 被引量:1

同被引文献11

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部