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作 者:汤桂芳[1] 袁霞[1] 陈瑞玲[1] 姜友珍[1]
出 处:《新医学》2009年第7期436-438,共3页Journal of New Medicine
基 金:广西壮族自治区卫生厅科研资助项目(Z2006136)
摘 要:目的:探讨HBV前S1抗原(pre-S1antigen,Pre-S1Ag)与HBV DNA、HBeAg的相关性,并评价Pre-S1Ag的临床应用价值。方法:对178例慢性乙型病毒性肝炎(慢乙肝)患者采用ELISA法检测Pre-S1Ag、HBeAg,采用荧光定量PCR法检测HBV DNA,比较Pre-S1Ag、HBeAg与HBV DNA的诊断符合率,并根据HBV DNA载量分为低复制组、中等复制组及高复制组,分析HBV DNA载量与Pre-S1Ag阳性率的相关性。结果:178例的HBVDNA均为阳性,其中Pre-S1Ag阳性144例(80.9%),Pre-S1Ag阴性34例(19.1%);HBeAg阳性112例(62.9%),HBeAg阴性66例(37.1%)。Pre-S1Ag、HBeAg与HBV DNA的诊断符合率分别为80.9%、62.9%,上述两诊断符合率比较差异有统计学意义(P<0.05)。112例HBeAg阳性慢乙肝者中,Pre-S1Ag的阳性率80.4%;66例HBeAg阴性慢乙肝者中,Pre-S1Ag阳性率82%。HBV高复制组的Pre-S1Ag阳性率(93%)高于中等复制组(80%)和低复制组(64%),且HBV DNA载量与Pre-S1Ag的阳性率呈正相关(r=0.293,P<0.01)。结论:Pre-S1Ag与HBV DNA有较好的相关性,在无法开展HBV DNA检测的基层医院,对于HBeAg阴性慢乙肝患者应增加检测Pre-S1Ag,以提高检测的准确度。Objective: To investigate the relationship among HBV pre-S1 antigen (Pre-S1Ag), HBV DNA and HBeAg, and to evaluate the clinical significance of Pre-S1Ag. Methods:Serum HBeAg and Pre-S1Ag were de- tected by ELISA in 178 patients with chronic Hepatitis B. HBV DNA was tested by quantitative fluorescence PCR technique. The positive concordance rate of HBV DNA ( + )/Pre-S1Ag( + ) and HBV DNA( + )/HBeAg( + ) was compared. All patients were divided into three groups according to their HBV DNA levels: low duplication group, medium duplication group and high duplication group. The correlation between HBV DNA levels and Pre- SlAg was analyzed. Results:In 178 patients with HBV DNA( + ), Pre-S1Ag positive was 144 cases(80. 9% ) and Pre-S1Ag negative was 34 cases ( 19. 1% ). For HBeAg, 112 cases (62. 9% ) were positive and 66 cases (37. 1% ) were negative. The positive concordance rate of HBV DNA( + )/Pre-S1Ag( + ) and HBV DNA( + )/ HBeAg( + ) was 80. 9% and 62.9%, respectively, there was statistically significant(P 〈0. 05). In 112 cases with HBeAg( + ), the positive rate of Pre-S1Ag was 80.4%. In 66 HBeAg( - ) cases, the positive rate of Pre- SlAg was 82%. The positive rate of Pre-S1Ag (93%) in high duplication group was higher than in the medium's (80%) and low's(64% ). The level of HBV DNA was significantly related to the positive rate of Pre-S1Ag(r = 0. 293 ,P 〈0.01 ). Conclusion: There is a better correlation between the Pre-SIAg and HBV DNA. In order to en- hance the examination accuracy, Pre-S1Ag should be measured in chronic Hepatitis B patients with HBeAg( - ), if some hospitals are not able to detect HBV DNA.
关 键 词:乙型病毒性肝炎 乙型肝炎病毒 前S1抗原 乙型肝炎病毒脱氧核糖核酸 乙型肝炎E抗原
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