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代文成, 多力坤·买买提玉素甫, 热娜古丽·艾则孜, 乔艳辉, 彭晓梅, 哈木拉提·吾甫尔. 异常体液患者5-HTT基因多态性分布比较[J]. 中国公共卫生, 2009, 25(2): 162-164. DOI: 10.11847/zgggws2009-25-02-20
引用本文: 代文成, 多力坤·买买提玉素甫, 热娜古丽·艾则孜, 乔艳辉, 彭晓梅, 哈木拉提·吾甫尔. 异常体液患者5-HTT基因多态性分布比较[J]. 中国公共卫生, 2009, 25(2): 162-164. DOI: 10.11847/zgggws2009-25-02-20
DAI Wen-cheng, Dolikun·Mamatyusupu, Renagul·Aziz, . Study on serotonin transporter gene polymorphisms in patients with abnormal hilit[J]. Chinese Journal of Public Health, 2009, 25(2): 162-164. DOI: 10.11847/zgggws2009-25-02-20
Citation: DAI Wen-cheng, Dolikun·Mamatyusupu, Renagul·Aziz, . Study on serotonin transporter gene polymorphisms in patients with abnormal hilit[J]. Chinese Journal of Public Health, 2009, 25(2): 162-164. DOI: 10.11847/zgggws2009-25-02-20

异常体液患者5-HTT基因多态性分布比较

Study on serotonin transporter gene polymorphisms in patients with abnormal hilit

  • 摘要: 目的 探讨异常体液(根据维吾尔医学理论诊断标准和WHO诊断标准)与5-羟色胺转运体(5-HTT)基因启动子区和内含子2区多态性的相关性.方法 按维吾尔医学理论将患者分为4种体液,利用PCR技术检测102例异常黑胆质型患者、44例其他异常体液型患者和45例正常对照组的2种基因多态性的分布频率.结果 异常黑胆质型患者组、其他异常体液型患者组和对照组的5-HTT(5-HTTLPR)多态性的SS基因型频率分别为39.21%,40.90%,40.00%;S等位基因频率分别为65.19%,65.90%,62.22%,组间差异均元统计学意义.对照组的L/L纯合子基因型频率为15.56%,高于异常黑胆质型患者组的8.83%和其他异常体液型患者组的9.10%.5-HTT(5-HT-TVNTR)多态性各基因型(12/12,12/10,10/10)频率在异常黑胆质型患者组中分别为74.50%,20.59%,4.91%;在其他异常体液型患者组中分别为75.00%,20.45%,4.55%;在对照组中分别为77.77%,17.78%,4.45%,各基因型组间差异均无统计学意义.此外异常黑胆质型患者组5-HTTLPR和5-HTTVNTR的基因型和等位基因频率与其它异常体液型患者组间的差异也无统计学意义.结论 5-HTTLL/L纯合子基因型可能是异常体液疾病发病的保护因子,5-HTT基因多态性与异常体液患者组之间的关系尚需进一步探讨.

     

    Abstract: Objective To investigate the association between abnormal hilit(according to diagno sticcriteria of Uigurmedicine theory and WHO diagnostic criteria)and the seroton in transporter(5 HTT)genepolymorphisms in promoter(5 HTT LPR)and the variable number tandemrepeats(VNTRs)in intron2(5 HTTVN TR).Methods The patients were divided into four different body fluids groups according to Uigur medicine theory.Polymerase chain reaction(PCR)was used to detect genotype and allele frequencies of 5 HTTLPR and 5 HTTVN TR gene polymorphisms in 102 patientswith abnormal black savda,44 patients with other abnormal hilit and 45 normal control subjects.Results No significant difference for the SS geno type frequency and difference of Sallele frequency of 5 HTTL PR were revealed bewteen patients with abnormal black savda(39.21% vs 40.00%,65.19% vs 62.22%)and patients with other abnormal hilit(4.90% vs 40.00%,65.90% vs 62.22%)and normal control subjects.The normal control subjects tended to be more of L/L genotype(15.56%)than patients with abnormal black savda(8.83%)and patients with other abnormal hilit(9.10%).However,there was no difference in the distribution of 5 HTTV N TR(12/12,12/10,10/10)bewteen patients with abnormal black savda(74.50%,20.59%,4.91%)and patientswith other abnorm al hilit(75.00%,20.45%,4.55%)and normal control subjects(77.77%,17.7%,84.45%).On the other hand,no significant difference in the geno type frequency and the alle le frequency of 5 HTTW PR and 5 HTTL PR was revealed between patients with abnormal black savda and patients with other abnormal hilit(P>0.05).Conclusion 5 HTT LPR L/L geno type may be a protective factor for abnormal hilit.No corelation was found between polym orphisms of 5 HTT gene and patients with abnormal hilit.

     

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