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荧光定量PCR技术对1235例NGU病原体基因检测结果分析
引用本文:谭炳添,周晓兰,顾艳. 荧光定量PCR技术对1235例NGU病原体基因检测结果分析[J]. 遵义医学院学报, 2008, 31(4): 358-360
作者姓名:谭炳添  周晓兰  顾艳
作者单位:遵义医学院第五附属(珠海)医院,检验科,广东,珠海,519100
摘    要:目的用实时荧光定量PCR(FQ—PCR)技术准确定量检测非淋菌性尿道炎(NGu)中解脲支原体(UU)、沙眼衣原体(CT)基因,进一步了解UU、CT感染情况,为临床治疗提供依据。方法采用FQ—PCR技术检测标本1235份。结果UU阳性率是27.5%,其中男性UU阳性率是12.4%,女性UU阳性率是42.0%。CT阳性率是12.1%,其中男性CT率是11.2%,女性CT率是13.2%。UU感染率在男性、女性患者有极显著性差异(P〈0.01),而CT感染率在性别之间无显著性差异(P〉0.05)。结论实时荧光定量PCR检测UU、CT基因具有操作简单、反应时间短、重复性好、结果客观准确、敏感性和特异性好等优点,其结果对临床诊断、治疗有一定指导意义。

关 键 词:非淋菌性尿道炎(NGU)  沙眼衣原体  解脲支原体  实时荧光定量PCR

Detection and Analysis of the gene of causative agents of 1235 cases of non-gonococcal urethritis by fluorescence quantitative PCR
TAN Bing-tian,ZHOU Xiao-lan,GU Yan. Detection and Analysis of the gene of causative agents of 1235 cases of non-gonococcal urethritis by fluorescence quantitative PCR[J]. Acta Academiae Medicine Zunyi, 2008, 31(4): 358-360
Authors:TAN Bing-tian  ZHOU Xiao-lan  GU Yan
Affiliation:TAN Bing-tian,ZHOU Xiao-lan GU Yan (The fifth Affiliated ( Zhu Hai) Hospital of Zunyi Medical College,Guangdong 519100,China )
Abstract:Objective To detect quantitatively the gene of Ureaplasm urealyticum (UU) and Chlamydia trachomatis (CT) in non--gonococcal urethfitis by technology of fluorescence quantitative polymerase chain reaction (FQ-PCR),to understand further infections condition of UU and CT ,and to provide clinical treatment evidence to the disease. Methods Detection 1235 speciments by technology of FQ-PCR. Results the positive of UU was 27.5% of all these;male posiaive was 12.4%, and female was 42.0%0 the positive of CT was 12.1% of all these male posiaive was 11.2% ,and female was 13.2%. Infectious rates of UU had obvious statistics difference between males and females,but CT hadn't. Conclusions The fluorescence quantitative PCR assays showed advantages which were mainpulated simply,time--saving,more extra,more sensitive and more spectific in detecting CT and UU. FQ-PCR had directive meaning for dagnosis and treatmeat.
Keywords:NGU  UU  CT  fluorescence quantitative PCR assay  
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