慢性乙型肝炎伴与不伴肝纤维化患者t -调节细胞、血清丙氨酸转氨酶和天冬氨酸转氨酶的差异

Yostila Derosa, Nasrul Zubir, Raveinal Arnelis
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引用次数: 0

摘要

背景:乙型肝炎是由乙型肝炎病毒引起的急性或慢性肝脏炎症,可发展为肝硬化或肝癌。慢性乙型肝炎有很高的肝纤维化风险。慢性炎症与肝纤维化是相互关联的过程。本研究旨在确定t调节细胞、丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)在慢性乙型肝炎伴肝纤维化和不伴肝纤维化患者中的差异。方法:本研究采用横断面法,对巴东市其他医院内科M. Djamil Padang博士住院部和门诊部诊断为慢性乙型肝炎的患者进行为期6个月的研究。按纳入标准和排除标准连续取样。肝纤维化是通过纤维扫描诊断的。数据采用SPSS 21.0进行分析。结果:慢性乙型肝炎32例,肝纤维化50%。无肝纤维化的慢性乙型肝炎患者t调节细胞水平为2.08%,肝纤维化患者为2.25%,但差异无统计学意义(p 0.05)。无纤维化组平均ALT水平为19 IU/L (7IU/L- 71iu /L),肝纤维化组平均ALT水平为61 IU/L (13IU/L- 625iu /L)。无纤维化组AST平均水平为15.5 IU/L (10IU/L- 32iu /L),肝纤维化组AST平均水平为35.5 IU/L (10IU/L- 476iu /L)。两组间ALT、AST比较差异有统计学意义(p < 0.05)。合并肝纤维化的乙肝患者ALT和AST水平高于未合并肝纤维化的乙肝患者。结论:两组患者t调节细胞水平有差异,但差异无统计学意义。肝纤维化组ALT、AST水平升高,差异有统计学意义。
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The Differences of T-Regulator Cells, Alanine Aminotransferase Serum and Aspartate Aminotranspherase Between Hepatitis B Chronic Patients with and without Liver Fibrosis
Background: Hepatitis B is acute or chronic liver inflammation caused by hepatitis B viral and can progress to hepatic chirrosis or liver cancer. Chronic hepatitis B has a high risk for liver fibrosis. Chronic inflammation and liver fibrosis are interrelated processes. This study aimed to determine the differences in T-regulator cells, Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) between chronic hepatitis B patients with and without liver fibrosis.Method: This study used a cross-sectional method for patients diagnosed with chronic hepatitis B in the Inpatient and Outpatient Department of the Internal Medicine Department  DR. M. Djamil Padang and other hospitals in Padang city for 6 months. Samples were selected by consecutive sampling according to inclusion and exclusion criteria. Liver fibrosis is identified by fibroscan. Data were analyzed by SPSS 21.0.Results: thirty-two patients were diagnosed with chronic hepatitis B and 50% had liver fibrosis. The levels of T-regulator cells in chronic hepatitis B patients without liver fibrosis were 2.08% and liver fibrosis 2.25%, but this difference was not statistically significant (p 0.05). Mean ALT levels in the group without fibrosis were 19 IU/L (7IU/L-71IU/L) and liver fibrosis 61 IU / L (13IU/L-625IU/L). The mean AST level in the group without fibrosis were 15.5 IU/L (10IU/L-32IU/L) and liver fibrosis 35.5 IU/L (10IU/L-476IU/L). The difference between ALT and AST in the two groups was significant (p 0.05). Hepatitis B patients with liver fibrosis had higher ALT and AST levels than without fibrosis.Conclusion: There were differences levels of T-regulator cells in the two groups, but it was not statistically significant. ALT and AST levels were higher in the liver fibrosis group and statistically significant.
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