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焦阳, 马靖松, 邱晓惠, 杨秀贤, 王琳, 杨艳杰. TPH2基因交互作用与单相抑郁症关系[J]. 中国公共卫生, 2014, 30(6): 712-714. DOI: 10.11847/zgggws2014-30-06-05
引用本文: 焦阳, 马靖松, 邱晓惠, 杨秀贤, 王琳, 杨艳杰. TPH2基因交互作用与单相抑郁症关系[J]. 中国公共卫生, 2014, 30(6): 712-714. DOI: 10.11847/zgggws2014-30-06-05
JIAO Yang, MA Jing-song, QIU Xiao-hui.et al, . Interaction of tryptophan hydroxylase isoform genes in unipolar depression patients[J]. Chinese Journal of Public Health, 2014, 30(6): 712-714. DOI: 10.11847/zgggws2014-30-06-05
Citation: JIAO Yang, MA Jing-song, QIU Xiao-hui.et al, . Interaction of tryptophan hydroxylase isoform genes in unipolar depression patients[J]. Chinese Journal of Public Health, 2014, 30(6): 712-714. DOI: 10.11847/zgggws2014-30-06-05

TPH2基因交互作用与单相抑郁症关系

Interaction of tryptophan hydroxylase isoform genes in unipolar depression patients

  • 摘要: 目的了解色氨酸羟化酶2(TPH2)基因rs11178997和G1463A交互作用与单相抑郁症的关系。方法提取中国北方地区600例单相抑郁症患者(病例组)和600名健康对照者(对照组)基因组DNA,采用聚合酶链反应(PCR)技术扩增包含TPH2基因rs11178997、G1463A位点的DNA片段,应用TaqMan-MGB荧光定量PCR 技术检测TPH2基因rs11178997、G1463A位点的基因型。结果病例组与对照组SNP(单核苷酸多态性)基因型分布符合Hardy-Weinberg平衡定律(P>0.05);病例组rs11178997基因型A/A、A/T、T/T频率分别为23.0%(138/600)、43.0%(258/600)、34.0%(204/600),对照组分别为48.7%(292/600)、10.0%(60/600)、41.3%(248/600);病例组G1463A基因型A/A、A/G、G/G频率分别为40.7%(244/600)、11.8%(71/600)、47.5%(285/600),对照组分别为39.7%(238/600)、1.3%(8/600)、59.9%(354/600);病例组rs11178997等位基因A、T频率分别为44.5%(534/1 200)、55.5%(666/1 200),对照组分别为53.7%(644/1 200)、46.3(556/1 200);病例组G1463A等位基因A、G频率分别为46.6%(559/1 200)、53.4%(641/1 200),对照组分别为40.3%(484/1 200)、59.7(716/1 200)。TPH2基因rs11178997与G1463A位点基因型及等位基因频率在2组间的差异有统计学意义(P<0.05);携带rs11178997 T+ 与G1463A A+ 基因型的个体罹患抑郁症的风险显著性增加(OR=52.786,P<0.05)。结论TPH2基因rs11178997与G1463A的交互作用在单相抑郁症发病机制中具有重要意义。

     

    Abstract: ObjectiveTo explore the interaction between tryptophan hydroxylase-2(TPH-2)gene rs11178997 and G1463A in uniplor deression patients.MethodsWe collected peripheral blood specimens from 600 uniplor depression patients and 600 healthy controls in a mental hospital in Harbin city.PCR was used to detect the polymorphisms of rs11178997 and G1463A.The amplification of novel TPH2 gene rs11178997,G1463A was executed by TaqMan real-time-polymerase chain reaction(real-time-PCR).ResultsThe single nucleotide polymorphism(SNP)frequences of rs 1178997 and G1463A were not deviant from Hardy-Weinberg equilibrium in both case and control groups(P>0.05).Compared with the control group,significant differences in genotypes and alleles of TPH2 gene rs11178997 were observed in patient group(23.0% vs.48.7% for A/A,43.0% vs.10.0% for A/T,34.0% vs.41.3% for T/T,44.5% vs.53.7% for allele A,and 55.5% vs.46.3% for allele T;P<0.05 for all).Compared with the control group,significant differences in genotypes and alleles of TPH2 gene G1463A were observed in patient group(40.7% vs.39.7% for A/A,11.8% vs.1.3% for A/G,47.5% vs.59.9% for G/G,46.6% vs.40.3% for allele A,and 53.4% vs.59.7% for allele G;P<0.05 for all).Compared with the control group,significant differences in genotypes and alleles of TPH2 gene rs11178997,G1463A SNP were found in patient group,respectively(χ2=57.766,P=0.000;χ2=182.72,P=0.000;χ2=9.538,P=0.000;χ2=20.173,P=0.002).The interaction of TPH2 gene rs11178997 T+ and G1463A A+ was associated with depression(odds ratio=52.786,P<0.05).ConclusionThe interaction between rs11178997 and G1463A plays an important role in the pathogenesis of uniplor depression.

     

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