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苏州地区妇女宫颈人乳头状瘤病毒基因分型的研究
引用本文:龚培尧,李海,耿建祥,李丽,刘忠伦,王晓红,王宏景,夏林,夏思钧.苏州地区妇女宫颈人乳头状瘤病毒基因分型的研究[J].国际检验医学杂志,2013,34(23):3127-3128,3130.
作者姓名:龚培尧  李海  耿建祥  李丽  刘忠伦  王晓红  王宏景  夏林  夏思钧
作者单位:龚培尧 (徐州市妇幼保健院病理科,江苏徐州,221009); 李海 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 耿建祥 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 李丽 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 刘忠伦 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 王晓红 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 王宏景 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 夏林 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001); 夏思钧 (南京中医药大学附属第三医院病理科HPV协作组,江苏南京,210001);
基金项目:南京市卫生局中医专项资助项目(项目编号:2009-92)
摘    要:目的探讨苏州地区妇女宫颈感染人乳头状瘤病毒(HPV)的基因型分布及其临床意义。方法采用基因扩增结合基因芯片技术对4 862例宫颈上皮细胞标本进行23种HPV基因分型检测。结果宫颈上皮细胞HPV阳性率为31.74%(1543/4 862)。其中,一重感染、多重感染的阳性率分别为21.43%(1 042/4 862)、10.30%(501/4 862)。前7位高危型HPV分别为16、58、52、33、18、56、31型,占59.09%,而低危型HPV分别为11、6、43型,占23.70%。结论基因扩增结合基因芯片技术可应用于宫颈细胞HPV分型检测。

关 键 词:子宫颈  人乳头瘤病毒  基因型  芯片分析技术

A research of genotypes of human papillomavirus infected in cervix uteri of women in Suzhou region
Gong Peiyao,Li Hai,Geng Jianxiang,Li Li,Liu Zhonglun,Wang Xiaohong,Wang Hongjing,Xia Lin,Xia Sijun.A research of genotypes of human papillomavirus infected in cervix uteri of women in Suzhou region[J].International Journal of Laboratory Medicine,2013,34(23):3127-3128,3130.
Authors:Gong Peiyao  Li Hai  Geng Jianxiang  Li Li  Liu Zhonglun  Wang Xiaohong  Wang Hongjing  Xia Lin  Xia Sijun
Institution:1. Department of Pathology ,Xuzhou Health Hospital for Women and Children ,Xuzhou,Jiangsu 221009 ,China ;2. HPV Collaborative Group, Department of Pathology, Nanjing Hospital of Traditional Chinese Medicinethe Third Affiliated Hoslital of Nanjing University of Traditional Chinese Medicine ,Nanjing,Jiangsu 210001 ,China)
Abstract:Objective To investigate the genotype distribution of human papillomavirus(HPV)infected in cervix uteri of women in Suzhou region and its clinical significance.Methods Microarray gene amplification technique was employed to assay 23 kinds of HPV genotype in 4 862 samples of cervical epithelial cells.Results The HPV-positive rate of cervical epithelial cells was 31.74%(1 543/4 862).Among them,mono-infection rate and multiple infection rate were 21.43%(1 042/4 862) and 10.30%(501/4 862). The top seven high-risk HPV types were 16,58,52,33,18,56,31,accounting for 59.09%,while the low-risk HPV types were 11, 6,43,accounting for 23.70%.Conclusion Microarray gene amplification technique can be applied to assay HPV genotyping in cer- vical cells.
Keywords:cervix uteri  human papillomavirus  genotype  microchip analytical procedures
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