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Correlation of serum chemokine RANTES level with serum biochemical indices, HBeAg and HBV DNA load in patients with chronic hepatitis B / 中华实验和临床病毒学杂志
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-325595
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the level of the serum chemokine RANTES and its correlation with serum biochemical indices of liver function test, HBeAg and HBV DNA load in patients with chronic hepatitis B.</p><p><b>METHODS</b>144 patients with chronic hepatitis B (observed group) and 18 normal cases (control group) were enrolled in this study. The serum level of chemokine RANTES was detected with an ABC-ELISA assay. Statistical analysis was performed on the software of SPSS13.0.</p><p><b>RESULTS</b>The serum chemokine RANTES level in the observed group (3930.12 ng/ml 2856.96) ng/ml was significantly higher than that in the control group (329.46 ng/ml +/- 152.23) ng/ml. The results from the observed group indicated the positive correlation of serum RANTES level with indices of liver function test, including ALT (r = 0.197, P = 0.018), AST(r = 0.239, P = 0.004) and TBil (r = 0.316, P = 0.001), but did not with PTA (r = - 0.078, P = 0.357). Neither difference of serum chemokine RANTES level between HBeAg-positive group and HBeAg-negative group nor that between high HBV DNA load group (> or = 10(5) copies/ml) and low HBV DNA load group (< 10(5) copies/ml) were statistically significant (P = 0.407 and 0.185, respectively).</p><p><b>CONCLUSIONS</b>Serum chemokine RANTES level in patients with chronic hepatitis B elevates significantly and is not affected by HBeAg or HBV DNA load. Its positive correlation with indices of liver function test indicates that RANTES might play an important role in the pathogenesis of chronic hepatitis B.</p>
Subject(s)
Full text: Available Health context: SDG3 - Health and Well-Being / SDG3 - Target 3.3 End transmission of communicable diseases / SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Hepatitis / Digestive System Diseases Database: WPRIM (Western Pacific) Main subject: Physiology / Virology / Blood / Case-Control Studies / Hepatitis B virus / Chemokine CCL5 / Viral Load / Hepatitis B, Chronic / Diagnosis / Hepatitis B e Antigens Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adolescent / Adult / Aged / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Experimental and Clinical Virology Year: 2009 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being / SDG3 - Target 3.3 End transmission of communicable diseases / SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Hepatitis / Digestive System Diseases Database: WPRIM (Western Pacific) Main subject: Physiology / Virology / Blood / Case-Control Studies / Hepatitis B virus / Chemokine CCL5 / Viral Load / Hepatitis B, Chronic / Diagnosis / Hepatitis B e Antigens Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adolescent / Adult / Aged / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Experimental and Clinical Virology Year: 2009 Document type: Article
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