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NRG1-ErbB4基因多态性与局灶性癫痫易感性的关系

陈新元 吴晖 莫亚雄 韩雁冰 陈新利 朱文叶 黄蕊 唐薇

陈新元, 吴晖, 莫亚雄, 韩雁冰, 陈新利, 朱文叶, 黄蕊, 唐薇. NRG1-ErbB4基因多态性与局灶性癫痫易感性的关系[J]. 昆明医科大学学报, 2021, 42(6): 82-87. doi: 10.12259/j.issn.2095-610X.S20210607
引用本文: 陈新元, 吴晖, 莫亚雄, 韩雁冰, 陈新利, 朱文叶, 黄蕊, 唐薇. NRG1-ErbB4基因多态性与局灶性癫痫易感性的关系[J]. 昆明医科大学学报, 2021, 42(6): 82-87. doi: 10.12259/j.issn.2095-610X.S20210607
Xin-yuan CHEN, Hui WU, Ya-xiong MO, Yan-bing HAN, Xin-li CHEN, Wen-ye ZHU, Rui HUANG, Wen TANG. Association between NRG1-Erbb4 Polymor- phism and Focal Epilepsy[J]. Journal of Kunming Medical University, 2021, 42(6): 82-87. doi: 10.12259/j.issn.2095-610X.S20210607
Citation: Xin-yuan CHEN, Hui WU, Ya-xiong MO, Yan-bing HAN, Xin-li CHEN, Wen-ye ZHU, Rui HUANG, Wen TANG. Association between NRG1-Erbb4 Polymor- phism and Focal Epilepsy[J]. Journal of Kunming Medical University, 2021, 42(6): 82-87. doi: 10.12259/j.issn.2095-610X.S20210607

NRG1-ErbB4基因多态性与局灶性癫痫易感性的关系

doi: 10.12259/j.issn.2095-610X.S20210607
基金项目: 云南省科技计划基金资助项目(2017FE468(-037));云南省科技创新团队基金资助项目(2018HC008);云南省教育厅科学研究基金资助项目(2018JS197)
详细信息
    作者简介:

    陈新元(1994~),男,四川省渠县人,硕士,主要从事药学研究工作

    通讯作者:

    唐薇,E-mail: 964053452@qq.com

  • 中图分类号: R742.1

Association between NRG1-Erbb4 Polymor- phism and Focal Epilepsy

  • 摘要:   目的   研究云南地区患有局灶性癫痫人群的神经调节因子1(Neuregulin-1,NRG1)及其受体ErbB4基因的多态现象与局灶性癫痫易感性的关系。   方法   采用癫痫病例组和健康对照组对比分析,通过Snapshot检测方法,对云南地区的70例局灶性癫痫患者、64例健康对照者进行基因多态现象检测分析,研究对象样本均来自2020年3月到7月昆明医科大学第一附属医院。   结果   发现局灶性癫痫与NRG1(SNP rs35753505, T > C)的多态现象有相关性,NRG1(SNP rs35753505, T > C)基因型( P = 0.007)和等位基因(P = 0.005)的分布差异有统计学意义(P < 0.05)。与此同时,本研究还对NRG1下游受体ErbB4的基因多态性进行分析,发现ErbB4(SNPrs839523,G > A)基因型( P = 0.026)和等位基因(P = 0.013)、(SNPrs707284,A > G)基因型( P = 0.038)和等位基因(P = 0.018)的分布差异有统计学意义(P < 0.05),并且发现SNP rs707284携带的G/G基因型OR值为3.656(95% CI = 1.160-11.525)。   结论   携带突变纯合子G/G基因型的人群患癫痫的易感性较高,NRG1-ErbB4基因多态现象可能共同参与了局灶性癫痫的发生。
  • 表  1  检测基因引物序列(1)

    Table  1.   The primer sequence of tested genes (1)

    单核苷酸多态性 多态性 引物序列 产物长度/bp GC含量
    NRG1 rs35753505 [C/T] 上游引物5′-TTTAAGGCATCAGTTTTCAATAGC-3′
    下游引物5′-TGTCTGGAGAAGGTTTGGAATG-3′
    352 bp 32.1%
    rs6994992 [C/T] 上游引物5′-AGGATTGGATGTTTGAACCACT-3′
    下游引物5′- GGAGGGACAGGGTCATCACA-3′
    202 bp 50.0%
    rs62510682 [G/T] 上游引物5′-GCAAAATCAGCAACATCCTTC-3′
    下游引物5′-TTCCCACGTTATCTCCTACTCTT-3′
    194 bp 37.6%
    ErbB4 rs839523 [A/G] 上游引物5′-CACTTGGAGCATCCTCTTCTG-3′
    下游引物5′-ACTTGGCATGGCATTTGG-3′
    151 bp 38.4%
    rs7598440 [C/T] 上游引物5′-TCACCGCAGGGAATAAAACA-3′
    下游引物5′-CGATGGTAAAAGGCGTGCT-3′
    245 bp 48.2%
    rs707284 [A/G] 上游引物5′-CCACAACTGAGGGTTTTAGGAA-3′
    下游引物5′-TCAGAGGGTGGACGGTGG-3′
    387 bp 38.2%
    下载: 导出CSV

    表  1  检测基因引物序列(2)

    Table  1.   The primer sequence of tested genes (2)

    延伸引物方向 延伸产物 延伸引物长度 延伸引物
    Nrg1 R AG 22 5′-GGAAGCCATGTATCTTTATTTT-3′
    F CT 22 5′-CACCATGCAGGGTTCAAGTGAA-3′
    F GT 48 5′-TTTTTTTTTTTTTTTTTTTTTTTTTTATATGTGTGCAAACAGTTCTTA-3′
    ErbB4 F AG 32 5′-TTTTTTTTTTATTTGCAGATTATTTGCAGCTT-3′
    F CT 32 5′-TTTTTTTTTTGGCTACCCCTGGTAAGAGGGCT-3′
    F AG 42 5′-TTTTTTTTTTTTTTTTTTTTACATGTGCATGGAGTTTTTACC-3′
    下载: 导出CSV

    表  2  NRG1基因多态性与局灶性癫痫易感性关系[n(%)]

    Table  2.   The relationship between NRG1 gene polymorphism and susceptibility to focal epilepsy [n(%)]

    SNP 基因型/等位基因 癫痫组 对照组 Pa OR(95% CI) χ2 Pb
    rs35753505 T/T 13 (18.6) 19 (29.7) 1 9.996 0.007
    C/C 25 (35.7) 8 (12.5) 0.007 0.228 (0.078-0.663)
    C/T 32 (45.7) 37 (57.8) 0.540 0.767 (0.329-1.790)
    T 58 (41.4) 75 (58.6) 1 7.881 0.005
    C 82 (58.6) 53 (41.4) 0.005 0.500 (0.307-0.813)
    rs6994992 C/C 13 (18.6) 14 (21.9) 1 4.445 0.108
    T/C 30 (42.9) 36 (56.3) 0.869 1.078 (0.441-2.638)
    T/T 27 (38.6) 14 (21.9) 0.173 0.500 (0.185-1.354)
    C 56 (40.0) 64 (50.0) 1 2.704 0.100
    T 84 (60.0) 64 (50.0) 0.101 0.667 (0.411-1.082)
    rs62510682 G/G 61 (87.1) 56 (87.5) 1 0.004 0.951
    G/T 9 (12.9) 8 (12.5) 0.951 0.968 (0.349-2.683)
    T/T 0 (0) 0 (0) ----- -----------------
    G 131 (93.6) 120 (93.8) 1 0.004 0.952
    T 9 (6.4) 8(6.3) 0.952 0.970 (0.363-2.596)
      注:a为非条件 logistic 回归分析的P值,b为卡方检验的双侧P值。
    下载: 导出CSV

    表  3  ErbB4基因多态性与局灶性癫痫易感性的关系[n(%)]

    Table  3.   The relationship between the polymorphism of ErbB4 gene and the susceptibility of focal epilepsy [n(%)]

    SNP 基因型/等位基因 癫痫组 对照组 Pa OR(95% CI) χ2 Pb
    rs839523 G/G 15(21.4) 26(40.6) 1 7.333 0.026
    A/A 13(18.6) 5(7.8) 0.015 0.222(0.066~0.745)
    A/G 42(60.0) 33(51.6) 0.047 0.453(0.207~0.991)
    G 72(45.0) 85(66.4) 1 6.182 0.013
    A 68(55.0) 43(33.6) 0.013 0.536(0.327~0.878)
    rs7598440 C/C 18(25.7) 12(18.8) 1 1.129 0.569
    T/C 39(55.7) 37(57.8) 0.420 1.423(0.604~3.356)
    T/T 13(18.6) 15(23.4) 0.302 1.731(0.611~4.905)
    C 75(53.6) 61(47.7) 1 0.936 0.333
    T 65(46.4) 67(52.3) 0.334 1.267(0.784~2.049)
    rs707284 A/A 13(18.6) 6(9.4) 1 6.526 0.038
    A/G 41(58.6) 31(48.4) 0.368 1.638(0.560~4.795)
    G/G 16(22.9) 27(42.2) 0.027 3.656(1.160~11.525)
    A 67(47.9) 43(33.6) 1 5.622 0.018
    G 73(52.1) 85(66.4) 0.018 1.814(1.107~2.975)
      注:a为非条件 logistic 回归分析的P值;b为卡方检验的双侧P值。
    下载: 导出CSV
  • [1] 吴洵昳. 利用膜片钳技术探究内向整流钾离子通道Kir2.3在癫痫发病机制中的作用[C]. 中国抗癫痫协会脑电图与神经电生理分会. 第六届CAAE脑电图与神经电生理大会会刊. 中国抗癫痫协会脑电图与神经电生理分会: 中国抗癫痫协会, 2018: 21.
    [2] 陈新元, 武羽洁, 季雨伟, 等. NRG1/ErbB4与癫痫相关性及其遗传易感性研究进展[J]. 中国实用神经疾病杂志,2020,23(1):89-92.
    [3] Chuang S-H, Reddy D S. Genetic and molecular regulation of extrasynaptic gaba-a receptors in the brain: therapeutic insights for epilepsy[J]. The Journal of Pharmacology and Experimental Therapeutics,2018,364(2):180-179. doi: 10.1124/jpet.117.244673
    [4] GarciaRosa Sheila, de Freitas Brenha Bianca, da Rocha Vinicius Felipe, et al. Personalized medicine using cutting edge technologies for genetic epilepsies[J]. Curr Neuropharmacol, 2020, 18(期): 1.

    Garcia Rosa Sheila, de Freitas Brenha Bianca, da Rocha Vinicius Felipe, et al. Personalized medicine using cutting edge technologies for genetic epilepsies[J]. Curr Neuropharmacol,2021,19(6):813-831.
    [5] Lascano Agustina M, Korff Christian M, Picard fabienne. seizures and epilepsies due to channelopathies and neurotransmitter receptor dysfunction[J]. A Parallel between Genetic and Immune Aspects,2016,7(4):197-209.
    [6] Scheffer I E, Berkovic S, Capovilla G, et al. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology[J]. Epilepsia,2017,58(4):512-521. doi: 10.1111/epi.13709
    [7] Kataria H, Alizadeh A, Karimi-Abdolrezaee S. Neuregulin-1/ErbB network: An emerging modulator of nervous system injury and repair[J]. Prog neurobiol, 2019, 180(期): 101643.

    Kataria H, Alizadeh A, Karimi Abdolrezaee S. Neuregulin-1/ErbB network: An emerging modulator of nervous system injury and repair[J]. Prog neurobiol,2019,180(9):101643.
    [8] Grieco S F, Wang G, Mahapatra A, et al. Neuregulin and ErbB expression is regulated by development and sensory experience in mouse visual cortex[J]. J Comp Neurol,2020,528(3):419-432. doi: 10.1002/cne.24762
    [9] Rahman-Enyart A, Lai C, Prieto A L. Neuregulins 1, 2, and 3 Promote Early Neurite Outgrowth in ErbB4-Expressing Cortical GABAergic Interneurons[J]. Mol Neurobiol,2020(6):1-21.
    [10] Barnes A, Isohanni M, Barnett J H, et al. Neuregulin-1 genotype is associated with structural differences in the normal human brain[J]. Neuroimage,2012,59(3):2057-2061. doi: 10.1016/j.neuroimage.2011.10.007
    [11] Mei L, Nave K A. Neuregulin-ErbB Signaling in the Nervous System and Neuropsychiatric Diseases[J]. Neuron,2014,83(1):27-49. doi: 10.1016/j.neuron.2014.06.007
    [12] Zhu W Y, Jiang P, He X, et al. Contribution of NRG1 Gene Polymorphisms in Temporal Lobe Epilepsy[J]. J Child Neurol,2016,31(3):271-276. doi: 10.1177/0883073815589757
    [13] Liang D, Fan F, Ding W, et al. Increased Seizure Susceptibility for Rats Subject to Early Life Hypoxia Might Be Associated with Brain Dysfunction of NRG1-ErbB4 Signaling in Parvalbumin Interneurons[J]. Molecular Neurobiology, 2020, 卷(期): 1-10.

    Liang D, Fan F, Ding W, et al. Increased Seizure Susceptibility for Rats Subject to Early Life Hypoxia Might Be Associated with Brain Dysfunction of NRG1-ErbB4 Signaling in Parvalbumin Interneurons[J]. Molecular Neurobiology,2020,57(9):5276-5285.
    [14] 王艳雪, 李坪, 张歆悦, 等. Neuregulin-1及其受体ErbB在中枢神经系统损伤修复中作用的研究进展[J]. 神经解剖学杂志,2019,35(01):83-87.
    [15] Tan G H, Liu Y Y, Hu X L, et al. Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons[J]. Nat Neurosci,2012,15(2):258-266. doi: 10.1038/nn.3005
    [16] Li K X, Lu Y M, Xu Z H, et al. Neuregulin 1 regulates excitability of fast-spiking neurons through Kv1.1 and acts in epilepsy[J]. Nat Neurosci,2012,15(2):267-273. doi: 10.1038/nn.3006
    [17] 黄薇隗, 彭伟, 江蓉, 等. NRG1基因多态性与颞叶癫痫的关系[J]. 神经损伤与功能重建,2018,13(10):531-533.
    [18] Deng C, Pan B, Engel M, et al. Neuregulin-1 signalling and antipsychotic treatment[J]. Psychopharmacology (Berl.),2013,226(2):201-215. doi: 10.1007/s00213-013-3003-2
    [19] Dedeurwaerdere S, Boets S, Janssens P, et al. In the grey zone between epilepsy and schizophrenia: alterations in group II metabotropic glutamate receptors[J]. Acta Neurol Belg,2015,115(3):221-232. doi: 10.1007/s13760-014-0407-7
    [20] Amini E, Rezaei M, Mohamed Ibrahim N, et al. A Molecular Approach to Epilepsy Management: from Current Therapeutic Methods to Preconditioning Efforts[J]. Mol Neurobiol,2015,52(1):492-513. doi: 10.1007/s12035-014-8876-5
    [21] Liang Shi, Clare M. Bergson. Neuregulin 1: an intriguing therapeutic target for neurodevelopmental disorders, 2020, 10(1): 612-618.
    [22] Schmitt A, Koschel J, Zink M, et al. Gene expression of NMDA receptor subunits in the cerebellum of elderly patients with schizophrenia[J]. Eur Arch Psychiatry Clin Neurosci,2010,260(2):101-111. doi: 10.1007/s00406-009-0017-1
    [23] Butler K M, Moody O A, Elisabeth S, et al. De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsy[J]. Brain,2018,141(8):2392-2405. doi: 10.1093/brain/awy171
    [24] Lascano A M, Korff C M, Picard F. Seizures and Epilepsies due to Channelopathies and Neurotransmitter Receptor Dysfunction: A Parallel between Genetic and Immune Aspects[J]. Mol Syndromol,2016,7(4):197-209. doi: 10.1159/000447707
    [25] Koepp M J, Hammers A, D A Riaño Barros, et al. NMDA receptor binding in focal epilepsies[J]. J Neurol Psychiatry,2015,86(10):1150-1157. doi: 10.1136/jnnp-2014-309897
    [26] Backx L, Ceulemans B, Vermeesch J R, et al. Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4[J]. Eur J Hum Genet,2009,17(3):378-382. doi: 10.1038/ejhg.2008.180
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