Tarana Gupta, Hari K Aggarwal, Sandeep Goyal, Virendra Singh
{"title":"基因3型对慢性丙型肝炎肝硬化的预测","authors":"Tarana Gupta, Hari K Aggarwal, Sandeep Goyal, Virendra Singh","doi":"10.5005/jp-journals-10018-1311","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Genotype 3 increases fibrosis in chronic hepatitis C (CHC).</p><p><strong>Aim: </strong>To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC.</p><p><strong>Materials and methods: </strong>Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May 2017 were enrolled in the study. We compared biochemical and hematological parameters, HCV RNA load, transient elastography, and ultrasound, in genotype 3 and nongenotype 3 patients. Cirrhosis was diagnosed in patients with liver stiffness measurement (LSM) ≥13 kPa.</p><p><strong>Results: </strong>Out of 835 CHC patients, overall, genotype 3 had higher LSM (11.3 vs 7.62, <i>p</i> = 0.01), higher aspartate aminotransferase (AST) (88.4 vs 68.6, <i>p</i> = 0.02), and low platelets (228.4 vs 261, <i>p</i> = 0.03) with higher prevalence of cirrhosis (115/415 vs 25/245, <i>p</i> = 0.01) than nongenotype 3. However, decompensation rates were not significantly different between two groups (32/115 vs 7/25, <i>p</i> = 0.98). The subgroup analysis revealed that cirrhotic genotype 3 had advanced age (50 vs 35, <i>p</i> < 0.01), male predominance, and higher AST (74.4 vs 57, <i>p</i> = 0.01) as compared to noncirrhotic genotype 3 patients. On multivariate analysis, age and AST values were higher in cirrhotic than noncirrhotic genotype 3 patients.</p><p><strong>Conclusion: </strong>Genotype 3 patients have higher prevalence of cirrhosis and fibrosis compared to nongenotype 3 patients; however, decompensation was not different between two groups.</p><p><strong>How to cite this article: </strong>Gupta T, Aggarwal HK, Goyal S, <i>et al.</i> Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3. Euroasian J Hepato-Gastroenterol 2020;10(1):7-10.</p>","PeriodicalId":11992,"journal":{"name":"Euroasian Journal of Hepato-Gastroenterology","volume":"10 1","pages":"7-10"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/92/d8/ejohg-10-7.PMC7376599.pdf","citationCount":"3","resultStr":"{\"title\":\"Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3.\",\"authors\":\"Tarana Gupta, Hari K Aggarwal, Sandeep Goyal, Virendra Singh\",\"doi\":\"10.5005/jp-journals-10018-1311\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Genotype 3 increases fibrosis in chronic hepatitis C (CHC).</p><p><strong>Aim: </strong>To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC.</p><p><strong>Materials and methods: </strong>Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May 2017 were enrolled in the study. We compared biochemical and hematological parameters, HCV RNA load, transient elastography, and ultrasound, in genotype 3 and nongenotype 3 patients. Cirrhosis was diagnosed in patients with liver stiffness measurement (LSM) ≥13 kPa.</p><p><strong>Results: </strong>Out of 835 CHC patients, overall, genotype 3 had higher LSM (11.3 vs 7.62, <i>p</i> = 0.01), higher aspartate aminotransferase (AST) (88.4 vs 68.6, <i>p</i> = 0.02), and low platelets (228.4 vs 261, <i>p</i> = 0.03) with higher prevalence of cirrhosis (115/415 vs 25/245, <i>p</i> = 0.01) than nongenotype 3. However, decompensation rates were not significantly different between two groups (32/115 vs 7/25, <i>p</i> = 0.98). The subgroup analysis revealed that cirrhotic genotype 3 had advanced age (50 vs 35, <i>p</i> < 0.01), male predominance, and higher AST (74.4 vs 57, <i>p</i> = 0.01) as compared to noncirrhotic genotype 3 patients. On multivariate analysis, age and AST values were higher in cirrhotic than noncirrhotic genotype 3 patients.</p><p><strong>Conclusion: </strong>Genotype 3 patients have higher prevalence of cirrhosis and fibrosis compared to nongenotype 3 patients; however, decompensation was not different between two groups.</p><p><strong>How to cite this article: </strong>Gupta T, Aggarwal HK, Goyal S, <i>et al.</i> Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3. 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引用次数: 3
摘要
背景:基因3型增加慢性丙型肝炎(CHC)的纤维化。目的:探讨丙型肝炎病毒(HCV)基因型对CHC患者肝脏疾病患病率和严重程度的影响。材料与方法:2016年6月至2017年5月,949例抗- hcv阳性患者入组研究。我们比较了基因3型和非基因3型患者的生化和血液学参数、HCV RNA负荷、瞬时弹性成像和超声。肝硬度测量值(LSM)≥13 kPa时诊断为肝硬化。结果:在835例CHC患者中,总体而言,基因3型比非基因3型有更高的LSM (11.3 vs 7.62, p = 0.01)、更高的天冬氨酸转氨酶(AST) (88.4 vs 68.6, p = 0.02)、低血小板(228.4 vs 261, p = 0.03)和更高的肝硬化患病率(115/415 vs 25/245, p = 0.01)。然而,两组失代偿率无显著差异(32/115 vs 7/25, p = 0.98)。亚组分析显示,与非肝硬化基因3型患者相比,肝硬化基因3型患者年龄较大(50 vs 35, p < 0.01),男性居多,AST较高(74.4 vs 57, p = 0.01)。在多变量分析中,肝硬化患者的年龄和AST值高于非肝硬化基因3型患者。结论:基因3型患者肝硬化和纤维化发生率高于非基因3型患者;然而,失代偿在两组之间没有差异。如何引用本文:Gupta T, Aggarwal HK, Goyal S,等。基因3型对慢性丙型肝炎肝硬化的预测中华肝病与胃肠病杂志[J]; 2010;10(1):7-10。
Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3.
Background: Genotype 3 increases fibrosis in chronic hepatitis C (CHC).
Aim: To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC.
Materials and methods: Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May 2017 were enrolled in the study. We compared biochemical and hematological parameters, HCV RNA load, transient elastography, and ultrasound, in genotype 3 and nongenotype 3 patients. Cirrhosis was diagnosed in patients with liver stiffness measurement (LSM) ≥13 kPa.
Results: Out of 835 CHC patients, overall, genotype 3 had higher LSM (11.3 vs 7.62, p = 0.01), higher aspartate aminotransferase (AST) (88.4 vs 68.6, p = 0.02), and low platelets (228.4 vs 261, p = 0.03) with higher prevalence of cirrhosis (115/415 vs 25/245, p = 0.01) than nongenotype 3. However, decompensation rates were not significantly different between two groups (32/115 vs 7/25, p = 0.98). The subgroup analysis revealed that cirrhotic genotype 3 had advanced age (50 vs 35, p < 0.01), male predominance, and higher AST (74.4 vs 57, p = 0.01) as compared to noncirrhotic genotype 3 patients. On multivariate analysis, age and AST values were higher in cirrhotic than noncirrhotic genotype 3 patients.
Conclusion: Genotype 3 patients have higher prevalence of cirrhosis and fibrosis compared to nongenotype 3 patients; however, decompensation was not different between two groups.
How to cite this article: Gupta T, Aggarwal HK, Goyal S, et al. Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3. Euroasian J Hepato-Gastroenterol 2020;10(1):7-10.