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慢性乙型肝炎患者血清HBV DNA载量与肝组织病理改变的分析[J]. 中山大学学报(医学科学版), 2012,33(4).
Investigation on Serum HBV Viral Loads and Changes of Liver Pathological Features in 158 Patients with Chronic Hepatitis B[J]. Journal of Sun Yat-sen University (Medical Sciences), 2012, 33(4).
【目的】 探讨慢性乙型肝炎患者血清HBV DNA载量与肝组织病理改变的关系?【方法】 158例慢性乙肝患者根据血清HBeAg分为HBeAg阳性组和阴性组
回顾性分析血清HBV DNA载量与肝组织病理炎症分级?纤维化分期之间的关系?【结果】 HBeAg阳性组105例与HBeAg阴性组53例血清HBV DNA载量(lg copies/mL)分别为6.6 ± 1.9和4.8 ± 2.5
二者相比P = 0.000?HBeAg阳性组肝组织炎症活动度G0~1 6例?G2 74例?G3~4 25例
其血清HBV DNA载量(lg copies/mL)分别为5.6 ± 1.1?6.5 ± 2.0?7.0 ± 1.5
三者血清HBV DNA载量无差异(P = 0.250);肝组织纤维化程度S0~1 23例?S2 56例?S3~4 26例
其血清HBV DNA载量(lg copies/mL)分别为6.6 ± 1.8?6.6 ± 2.0?6.6 ± 1.6
三者血清HBV DNA载量无差异(P = 0.996)?HBeAg阴性组肝组织炎症活动度G0~1 8例?G2 17例?G3~4 28例
其血清HBV DNA载量(lg copies/mL)分别为2.1 ± 1.9?4.7 ± 2.2?5.6 ± 2.3
G2?G3~4者血清HBV DNA载量较G0~1者高(P = 0.001)
G2与G3~4者血清HBV DNA载量无差异(P = 0.332);肝组织纤维化程度S0~1 10例?S2 25例?S3~4 18例
其血清HBV DNA载量(lg copies/mL)分别为2.7 ± 3.2?5.1 ± 1.8?5.4 ± 2.4
S2?S3~4者血清HBV DNA载量较S0~1者高(P = 0.005)
S2与S3~4者血清HBV DNA载量无差异(P = 0.745)?【结论】 HBeAg阳性乙肝患者血清HBV DNA载量与肝组织炎症及纤维化程度无关?HBeAg阴性乙型肝炎患者血清HBV DNA载量较高者其肝组织炎症及纤维化程度均较高?
【Objective】 To investigate the relationship between serum HBV DNA loads and liver pathological changes in the patients with chronic hepatitis B. 【Methods】 The relationship among HBV DNA loads
live histological inflammation grades and fibrosis stages of 158 cases was analyzed. 【Results】 The serum HBV DNA loads (lg copies/mL) in HBeAg-positive group with inflammation grades G0~1 (6 patients)
G2 (74 patients) and G3~4 (25 patients) were 5.6 ± 1.1
6.5 ± 2.0 and 7.0 ± 1.5
respectively. There was no significant difference in the patients of three inflammation grades (P = 0.250). The serum HBV DNA loads in HBeAg-positive group with liver tissues fibrosis stages of S0~1 (23 patients)
S2 (56 patients)
S3~4 (26 patients) were 6.6 ± 1.8
6.6 ± 2.0
6.6 ± 1.6
respectively
the difference was not significant (P = 0.996). The serum HBV DNA loads in HBeAg-negative group with inflammation grades G0~1 (8 patients)
G2(17 patients) and G3~4 (28 patients) were 2.1 ± 1.9
4.7 ± 2.2 and 5.6 ± 2.3 respectively. The serum HBV DNA level in patients with G2 and G3~4 inflammation grades was significant higher than in patients with G0~1 inflammation grades (P = 0.001). The serum HBV DNA loads in HBeAg-negative group with liver tissues fibrosis stages of S0~1(10 patients)
S2 (25 patients)
S3~4 (18 patients) were 2.7 ± 3.2
5.1 ± 1.8
5.4 ± 2.4 respectively. The serum HBV DNA level in patients with fibrosis stages of S2 and S3~4 was significant higher than in patients with fibrosis stages of S0~1 (P = 0.005). 【Conclusions】 The serum HBV DNA level does not correlate with the inflammation grades and fibrosis stages of liver tissues in HBeAg-positive patients. The serum HBV DNA loads display a positive correlation with the inflammation grades and fibrosis stages of liver tissues in HBeAg-negative patients.
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