期刊文献+

免疫基因稀有变异与精神分裂症相关性

下载PDF
导出
摘要 目的探究免疫基因稀有变异累积与精神分裂症病因学机制的相关性。方法对94例首发精神分裂症患者和134名正常对照进行全基因组外显子测序,并从Reactome数据库中获得与免疫相关的生物通路。应用KGGseq软件对测序数据进行质量控制以及探究稀有变异与精神分裂症病理机制的相关性。结果 TYK2基因(P<0.0)以及4个生物通路(AUTOIMMUNE_THYROID_DISEASE(P=0.001)、TRANSLOCATION_OF_ZAP_70_TO_IMMUNOLOGICAL_SYNAPSE(P=0.016)、Disease(P=0.034)、Adaptive Immune System(P=0.021))与精神分裂症相关。结论免疫通路可能与精神分裂病因学机制相关,但需要在后续更大的样本中进一步验证。
出处 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2018年第3期182-185,共4页 Chinese Journal of Nervous and Mental Diseases
基金 国家自然基金重点项目(编号:81630030 81130024) 四川省卫生和计划生育委员会科研项目(编号:17PJ079) 西南医大-泸州市联合项目(编号:2017LZXNYD-J33) 四川省教育厅重点项目(编号:18ZA0534)
  • 相关文献

参考文献1

二级参考文献12

  • 1Sullivan PF, Kendler KS, Meale MC, et al. Schizophrenia as acomplex trait: evidence from a meta-analysis of twin studies[J].Arch Gen Psychiatry,2003,60(12):1187-1192.
  • 2Maher B. The case of the missing heritability[J]. Nature,2008,458(7218):18-21.
  • 3So HC, Gui AH, Chemy SS, et al. Evaluating the heritability ex-plained by known susceptibility variants: a survey of ten com-plex diseases[J]. Genet Epidemiol,2011,35(5):310-317.
  • 4Falconer DS. The inheritance of liability to certain diseases, es-timated from the incidence among relatives[J]. Ann Hum Genet,1965’29(1):51-76.
  • 5Hindorff LA,Sethupathy P, Junkins HA, et al. Potential etiolog-ic and functional implications of genome-wide association locifor human diseases and traits[J]. Proc Natl Acad Sci USA,2009,106(23):9362-9367.
  • 6Bhugra D. The global prevalence of schizophrenia[J]. PloS Med,2005,2(5): e151.
  • 7Shifman S, Johannesson M, Bronstein M, et al. Genome-wide as-sociation identifies a common variant in the reelin gene that in-creases the risk of schizophrenia only in women[J]. PloS Genet,2008,4(2): e28.
  • 8Sullivan PF, Lin D,Tzeng JY, et al. Genomewide association forschizophrenia in the CATIE study: result of stage 1[J]. Mol Psy-chiatry,2009,14(12):1144.
  • 9Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heri-tability of complex diseases[J]. Nature,2009,461(7265):747-753.
  • 10Lee SH, Wray NR, Goddard ME, et al. Estimating missing heri-tability for disease from genome-wide association studies[J]. AmJ Hum Genet,2011,88(3):294-305.

共引文献5

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