| Abstract|| |
Background: In hepatitis C virus (HCV), infection viral and IL28B genotype along with many clinical and biochemical factors can influence response rates to pegylated interferon plus ribavirin (Peg-IFN-a/R) therapy and progression to chronic hepatitis C (CHC). Aims: The present study was conducted to determine the effect of biochemical and risk factors on treatment outcome in CHC patients in relation to their viral and host genotype. Settings and Design: The present study was a prospective Pe- IFN efficacy study consisting of Peg-IFN-a/R therapy for 24–48 weeks including 250 HCV infected patients. Materials and Methods: Biochemical parameters were determined by Beckman Coulter AU680 automated analyzer. HCV and Interleukin 28B (IL28B) genotyping were carried out by polymerase chain reaction-restriction fragment length polymorphism and viral load was determined by quantitative real-time PCR. Results: Wild outnumbered the variant genotypes in rs 12979860, rs 12980275, and rs 8099917 SNP of IL28B gene. Sustained virological response (SVR) SVR and viral genotype were significantly associated with age, hepatic steatosis, low-grade varices, and serum aspartate transaminase levels (at the end of treatment) (P < 0.05). In addition, SVR was significantly influenced by body mass index (BMI), insulin resistance, serum low-density lipoprotein , and ferritin levels (P < 0.05). Viral genotype 1 infected patients had higher serum cholesterol and triglyceride levels (P < 0.05). Conclusions: Although the IL28B sequence variation is the major factor that can influence response rates to antiviral therapy, viral and biochemical factors also have a definite role to play in the diagnosis, etiology, and treatment outcome in HCV-infected patients.
Keywords: Biochemical, chronic hepatitis C, IL28B, pegylated interferon, viral genotype
|How to cite this article:|
Shoukat A, Khan MS, Mudassar S, Kawoosa Z, Shah AH, Zargar SA. The role of biochemical variations and genotype testing in determining the virological response of patients infected with hepatitis C virus. J Global Infect Dis 2018;10:89-98
|How to cite this URL:|
Shoukat A, Khan MS, Mudassar S, Kawoosa Z, Shah AH, Zargar SA. The role of biochemical variations and genotype testing in determining the virological response of patients infected with hepatitis C virus. J Global Infect Dis [serial online] 2018 [cited 2019 Sep 15];10:89-98. Available from: http://www.jgid.org/text.asp?2018/10/2/89/232997
| Introduction|| |
Hepatitis C virus (HCV) is a positive-stranded RNA virus that chronically infects 130–150 million people comprising of nearly 3% of the world population. Approximately 7,00,000 people die each year from hepatitis C-related liver diseases. Infection with HCV induces a wide range of innate and adaptive immune responses that achieve permanent control of HCV in 20% to 50% of infected individuals. Most HCV infections persist (70%–80%), and about 30% of individuals with a persistent infection develop chronic liver diseases, including cirrhosis, and hepatocellular carcinoma (HCC). A variety of host, viral, and environmental factors are associated with the rate of progression of fibrosis and cirrhosis. Obesity is a metabolic risk factor for the development of HCC in the setting of chronic hepatitis C (CHC). Males, diabetic patients, smokers, and patients with increased hepatic iron are more likely to have advanced fibrosis. Lipid metabolism is profoundly disturbed in HCV infection. Hepatic steatosis as well as superimposed steatohepatitis is important risk factors for fibrosis progression in CHC. In individuals with CHC, viral load and elevated serum alanine transaminase (ALT) levels may have clinical relevance.
The goal of treating CHC patients with peginterferon plus ribavirin and direct acting antivirals (DAA's) is to eradicate the virus so as to attain SVR (SVR12 and SVR24); defined as viremia after completion of antiviral therapy for chronic HCV infection., Although there are DDA's such as telaprevir and boceprevir ( first generation); faldaprevir, simeprevir, and sofosbuvir (second generation) used nowadays for treatment of HCV infections, this treatment modality is expensive and not available at all medical centers. Still, long-acting pegylated interferon-α plus oral treatment with ribavirin (Peg-IFN-a/R) is considerably less potent than newer DAAs, and the end-of-treatment response is generally substantially higher than SVR24. Virus-specific characteristics but also clinical and biochemical parameters are among the baseline predictors of response to HCV treatment. Metabolic factors, such as high body mass index (BMI), presence and severity of liver steatosis, increasing homeostasis model assessment of insulin resistance score and older age, advanced stage of fibrosis and high viral load at baseline have been reported as negative predictors of response., Of known pretreatment variables, a powerful predictor of response to treatment is the viral genotype. Genotypes 2 and 3 have got a better outcome than genotypes 1 and 4 with an SVR of 75%–85% versus 45%–55%, respectively. Pretreatment ALT levels were found to be correlated positively with SVR.
Among the baseline predictors of response, the pretreatment host genetic polymorphisms have been the subject of recent, major studies. Several independent studies have consistently shown that single nucleotide polymorphisms (SNPs) near IL28B, which encodes the type III IFN-λ3 are strongly associated with the response to treatment of CHC and is assumed to explain the heterogeneity in HCV clearance across individuals. In particular, the homozygous wild genotypes TT at marker rs8099917, CC at marker rs12979860 and AA at marker rs12980275 are all associated with favorable treatment outcomes. These data have been confirmed in populations of different ancestry and HCV genotypes, and in various clinical scenarios.
Although, IL28B genotype is only one of many factors that can influence response rates to Peg-IFN-a/R therapy in HCV infection and progression to CHC it should be interpreted in the context of other clinical and biochemical factors. With this background in mind, the present study was conceived to study the correlation of IL28B polymorphism with clinical, biochemical and viral characteristics in patients with CHC in relation to treatment outcome (SVR) in the only tertiary care hospital in the valley of Kashmir.
| Materials and Methods|| |
The present work was a prospective Peg IFN efficacy study conducted in the Department of Gastroenterology and Clinical Biochemistry, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, Jammu and Kashmir, India between July 2012 and July 2015. The study was approved by the Ethical Committee of SKIMS.
Inclusion and exclusion criteria
The patients of any age group or sex with HCV-RNA level higher than 50 U/ml and not on treatment for HCV infection were included in the study. Patients with hemoglobin <7 g/dl, an absolute neutrophil count <500/mm 3, platelet count <50,000/mm 3, decompensated liver disease, active malignancies, severe psychiatric illness, the presence of HCC, the presence of autoimmune disorder, and on immunosuppressive drugs were excluded from the study.
The study included 250 HCV-infected patients. Blood samples were collected in clot activator vials for HCV serology and other serum biochemical parameters. Blood collected in ethylenediaminetetraacetic acid vials was used for HCV RNA levels, viral and host genotyping. A complete history was taken from all the patients before testing. All the procedures were performed after taking the proper consent from the patients and their caretakers.
Hepatitis C virus serology and genotyping
Serum samples were screened for Hepatitis C and anti-HCV antibodies using commercially available ELISA kits (HCV: Anti-HCV (ELISA): Murex, Biotech, Kyalami, South Africa). HCV genotyping was done using Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) employing the method of Chinchai et al.
Hepatitis C virus RNA levels and treatment responses
The HCV RNA was determined using a COBAS Amplicor HCV Monitor, v2.0 (Roche Diagnostics, Branchburg, NJ, USA) with a precision value of 50 IU/ml before, during and after the treatment.
Estimation of biochemical parameters like serum fasting blood glucose, albumin, cholesterol, triglyceride, low-density lipoprotein (LDL), bilirubin, ALT, aspartate transaminase (AST), ALP, ferritin, hemogram, vitamin D, vitamin B12 and TSH before the start of treatment. Investigations were performed on fully automated biochemistry analyzer (Beckman Coulter AU 680, USA) and Immunoassay Analyzer (Beckman Coulter Access II, USA). Some of the parameters such as ALT, AST, total leukocytic count (TLC), Hb, and platelet count were estimated at the end of the therapy to estimate the efficacy of therapy and complications associated with the drugs.
All patients were subjected to esophagogastroduodenoscopy (EGD) and ultrasonography. EGD was performed with an Olympus (Olympus, Japan) endoscope to look for varices. Abdominal ultrasonography was performed with the Aloka SSD 260 Ultrasonographer (Aloka Science and Humanity, Tokyo, Japan, with a 5 or 7.5 MHz transducer) on all patients.
IL28B gene polymorphism
PCR-RFLP was established for polymorphic analysis of rs 12979860, rs 12980275 and rs 8099917 SNPs in the promoter region of IL28B gene. Restriction digestion products for each were separated on 3% agarose gels stained with ethidium bromide for visualization on a ultraviolet trans-illuminator.
All qualitative variables were expressed as mean ± standard deviation Patient's baseline characteristics, and outcome measures were compared with the use of Student's t-test for parametric data, the Mann–Whitney U-test for nonparametric data for qualitative variables and Pearson's Chi-square test or Fisher's exact test for proportions. Multivariate analysis was performed by binary logistic regression for the parameters significant on univariate analysis. Statistical analysis was performed using the statistical software package SPSS (SPSS version 20 Inc., Chicago, IL, USA).
| Results|| |
During the study period of 3 years, 250 HCV-infected patients were enrolled in the study. [Table 1] summarizes the various methods for detection of HCV. Of the 250 patients, males were 170 (68.0%) and 80 (32.0%) were females. Majority of the patients were <50 years of age (74%; 185 of 250) and <70 kg of weight (69.8%; 117 of 250). Most of the patients had normal BMI (18.5–24.99 kg/m 2; 63.6%) followed by preobese class (25–29.99 kg/m 2; 25.2%), obese Class I (4.8%) underweight class (4.8%), obese Class II (1.6%) and underweight (4.8%). Patients were enrolled from almost every district of the state with a higher frequency of rural patients (55.6%; 139 of 250) [Figure 1]. Genotype 3 was the predominant genotype seen in 187 (74.8%) patients. [Table 2] depicts the frequency distribution of selected demographic and risk factors in 250 HCV-infected patients. [Table 3] depicts the levels of various physical parameters, biochemical factors altered due to complications associated with the drugs (Hb, TLC, Plt, PT, INR, etc.,) and the factors which influence outcome to treatment (HCV viral load, serum ferritin, vitamin D, vitamin B12 levels, triglyceride (TG), LDL, cholesterol, ALT, AST, etc).
|Figure 1: District wise distribution of hepatitis C virus infected patients|
Click here to view
|Table 2: Frequency distribution analysis of selected demographic and risk factors in hepatitis C patients (n=250)|
Click here to view
|Table 3: Levels of various patient characteristics and biochemical parameters|
Click here to view
In case of IL28B rs 12979860 polymorphism, 136 patients (54.4%) had wild genotype (CC) while as variant genotype (CT + TT) was seen in 114 patients (45.6%) [Table 4]. In rs 12980275 SNP 132 patients (52.8%) had AA genotype, whereas 118 patients (47.2%) had variant (AG + GG) genotype. Among the patients having nonalcoholic fatty liver disease (NAFLD) only 44% were having AA genotype compared to 61.8% of patients without NAFLD (P < 0.05) [Table 4]. In case of rs 8099917 SNP wild genotype (TT) was present in 59.6% compared to 40.4% having variant genotype (TG + GG). Wild-type genotype (TT) was present in 87.5% of patients with initially elevated levels of ALP with a significant association (P < 0.05). Association between IL28B genotypes, demographic, and biochemical characteristics of HCV patients is shown in [Table 4].
|Table 4: Association between rs12979860 (C to T) rs12980275 (A to G) and rs8099917 (T to G) genotypes, demographic and biochemical characteristics of hepatitis C virus patients|
Click here to view
Most of the patients having <50 years of age and <70 kg of weight achieved SVR (P < 0.05). Patients having normal baseline LDL levels responded very well to antiviral therapy compared to patients having elevated levels (P < 0.05). All the patients with normal ferritin levels achieved SVR (P < 0.05). Nearly 99% of patients who had normal AST levels after 24 weeks of treatment achieved SVR (P < 0.05). The association between SVR and majority of biochemical and risk factors of HCV patients is shown in [Table 5].
|Table 5: Association of various biochemical and risk factors of hepatitis C virus patients with sustained virological response and viral genotype|
Click here to view
Among the patients having <50 years of age 80.5% (149 of 185) were infected with genotype 3, while as only 19.5% of patients with virus having genotype 1 (P < 0.05). Among the patients infected with genotype 3 majority were having normal cholesterol and TG levels compared to elevated cholesterol and TG levels in patients infected with genotype 1 virus (P < 0.05). One hundred and ten of 187 (58.8%) patients with genotype 3 infection have normal AST levels at the end of treatment compared to patients with genotype 1 virus (26 of 63; 41.2%) (P < 0.05). The various parameters and laboratory investigations in relation to viral genotypes are shown in [Table 5].
[Table 6] depicts the multivariate analysis of various parameters with respect to viral and host genotype. Viral genotype was significantly associated with EGD, DM, TG, ALT Last, and AST (P < 0.05). All the three SNPs were significantly associated with each other (P < 0.05).
|Table 6: Multivariate analysis viral genotype and single nucleotide polymorphisms with various parameters by logistic regression|
Click here to view
| Discussion|| |
The basic aim of this study was to find out the association of viral and host genotypes with biochemical and other risk factors of HCV infected patients in relation to their treatment outcome. Outnumbering of favorable genotypes, good responders, genotype 3 virus, normal lipid profiles, nondiabetics along with normal vitamin status has been the major observations in this study. Similarly, apart from being significantly associated with each other a positive association of polymorphic SNPs with SVR, viral genotype, BMI, NAFLD, liver enzymes was observed along with a positive association of SVR and Viral genotype with age, NAFLD, diabetes mellitus, low-grade varices and lipid profile. Although many inferences have been made from this study, there is still a lot to be known from the investigations of this kind.
Since screening methods were the major source of detection of CHC in our study and probably males frequently participate in screening camps than females, it was no surprise that majority of our HCV infected patients were males (68%; 170 of 250) which is also consistent with many studies from India and abroad  [Table 1].
History of diabetes mellitus was present in 37 (14.8%) patients which is comparable to around 15% reported by Loguercio et al. but higher than 8.2% reported by Tohra et al. Recently, the presence and severity of hepatic steatosis have emerged as an important marker of progressive liver disease as well as virological response to anti-HCV therapy. The LDL receptors could permit the entry of HCV in hepatocytes leading to decreased serum LDL levels. Moreover, HCV replication could decrease intrahepatic cholesterol synthesis  supporting the presence of normal lipid profile in our set of patients [Table 2].
Majority of studies support the association of SNPs near the IL28B gene region encoding IFN lambda 3 with virological response and spontaneous elimination of the virus. Little is known about the IFN-λ family, but the evidence is mounting to support a role for them in the immune response to viral infections. Therefore, associations made between IL28B variants and HCV clearance in large-scale genetic studies provide an exciting mechanistic link between innate immunity and viral clearance. In this study, we genotyped three IL28B polymorphisms in 250 HCV infected patients in which the regularity of wild (favorable) allele was greater than variant alleles in all the analyzed SNPs giving the preliminary thought about the encouraging antiviral therapy response of HCV infected patients of valley. In case of rs12979860 SNP frequency of wild genotype (CC) was 54.4% which is higher than reported by previous studies. On elucidation of rs 12980275 SNP, the frequency of wild genotype (AA) was 52.8% which is higher than the frequency of 39% reported by Fattovich et al. 59.6% in our patients were wild (TT) for rs 8099917 SNP which is comparable to 56% reported by Fattovich et al. and many other studies  [Table 4].
The study showed significant association of IL28B rs 12979860 (CC) and rs 8099917 (TT) favorable alleles with HCV genotype 2/3 in agreement with several studies. Favorable genotypes of rs 12979860, rs 12980275, and rs 8099917 were found to be significantly associated with SVR (P < 0.05) which has previously been validated. The presence of variant alleles of IL28B SNPs has been linked to severe hepatic steatosis  in treaty with our study where we observed the higher percentage of variant allele for rs 12980275 SNP (P < 0.05) in patients with NAFLD. Surprisingly, wild allele of rs8099917 SNP was strongly associated with elevated baseline ALP levels and decreased platelet count (P < 0.05) which is in contrast to many studies  [Table 4].
Of the 250, 238 (96.8%) went on to attain SVR [Table 5]. Young patients (<50 years) were found to have an excellent outcome on treatment in compliance with many studies. Overweight and increased BMI is a negative predictor of SVR in HCV-infected patients. Since the mean weight and BMI was lower in our patients, the SVR was achieved in the majority of cases. Different studies have revealed that NAFLD, higher grades of fatty liver and hepatic steatosis are associated with poor SVR  in harmony with our observations. Almost all the patients with normal EGD attained SVR in our study supporting the presence of varices as an independent factor associated with poor SVR. The presence of insulin resistance and other factors associated with it such as diabetes mellitus and high LDL levels have been shown to have a negative impact on achieving SVR  in coherence with our study. As obese patients are known to have poor lymphatic circulation, this effect can limit the serum levels of pegylated IFN-a, leading to a reduction in SVR rates. Almost all the patients with SVR had normal AST levels at the end of treatment (P < 0.05) which does not support the majority of studies established previously. Although many studies have indicated that low Vitamin D and Vitamin B12 levels are associated with poor treatment outcome, we did not find any correlation between vitamin levels and SVR.
When stratified according to viral genotype the majority of patients were infected with genotype 3 alike many studies. In contrast to the majority of studies, there was a significantly higher percentage of patients with ≥50 years of age in genotype 3 than genotype 1 (58.5% vs. 41.5%; P = 0.0004). Nonalcoholic steatohepatitis (NASH) is a more advanced form of NAFLD in which there is inflammation in and around the fatty liver cells. NASH is now considered to be one of the main causes of cirrhosis. Among the patients with NAFLD, 31.5% were infected with genotype 1 virus as against 18.7% of patients in non-NAFLD group infected with the same genotype (P = 0.01) which is in contradiction to previous studies showing a strong association between genotype 3 and steatosis. High serum cholesterol and serum triglyceride were associated with genotype 1 (P = 0.008 and 0.001). Ching-Sheng et al. demonstrated the association of elevated lipid profile with viral genotype 2. Genotype 3 HCV has been correlated with dyslipidemia. However, the differential associations of lipid profiles between different viral genotypes remain largely unknown and deserve further studies. Of the various laboratory parameters which were significantly higher in genotype 1 compared to genotype 3 included AST levels (at the end of treatment; P = 0.01) in accordance with many studies  [Table 5].
| Conclusions|| |
Although the IL28B sequence variation is one of the major factors that can influence response rates to antiviral therapy, viral and biochemical factors also have a definite role to play in the diagnosis, etiology, and treatment outcome in HCV infected patients. A greater understanding of the mechanism behind the association of host and viral factors should provide insight into viral/host interactions leading to opportunities for improved anti-HCV therapeutics and more effective individualized therapy.
The authors are grateful to the technical and resident staff of the Department of Gastroenterology who helped us in procuring the HCV infected blood samples.
Financial support and sponsorship
This study was supported by SKIMS, Soura, Srinagar, Kashmir, 190011, India (Grant no # No. SIMS/ACAD/13-786).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Seeff LB. Natural history of chronic hepatitis C. Hepatology 2002;36:S35-46.
Shakil AO, Conry-Cantilena C, Alter HJ, Hayashi P, Kleiner DE, Tedeschi V, et al.
Volunteer blood donors with antibody to hepatitis C virus: Clinical, biochemical, virologic, and histologic features. The Hepatitis C Study Group. Ann Intern Med 1995;123:330-7.
Ohki T, Tateishi R, Sato T, Masuzaki R, Imamura J, Goto T, et al.
Obesity is an independent risk factor for hepatocellular carcinoma development in chronic hepatitis C patients. Clin Gastroenterol Hepatol 2008;6:459-64.
Pearlman BL, Traub N. Sustained virologic response to antiviral therapy for chronic hepatitis C virus infection: A cure and so much more. Clin Infect Dis 2011;52:889-900.
Thorlund K, Druyts E, Mills EJ. SVR12 is higher than SVR24 in treatment-naïve hepatitis C genotype 1 patients treated with peginterferon plus ribavirin. Clin Epidemiol 2014;6:49-58.
Vasudevan S, Shalimar, Kavimandan A, Kalra N, Nayak B, Thakur B, et al.
Demographic profile, host, disease and viral predictive factors of response in patients with chronic hepatitis C virus infection at a tertiary care hospital in North India. Indian J Med Res 2016;143:331-40.
] [Full text]
Zeuzem S, Hultcrantz R, Bourliere M, Goeser T, Marcellin P, Sanchez-Tapias J, et al.
Peginterferon alfa-2b plus ribavirin for treatment of chronic hepatitis C in previously untreated patients infected with HCV genotypes 2 or 3. J Hepatol 2004;40:993-9.
Berg T, Sarrazin C, Herrmann E, Hinrichsen H, Gerlach T, Zachoval R, et al.
Prediction of treatment outcome in patients with chronic hepatitis C: Significance of baseline parameters and viral dynamics during therapy. Hepatology 2003;37:600-9.
Rauch A, Kutalik Z, Descombes P, Cai T, Di Iulio J, Mueller T, et al.
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: A genome-wide association study. Gastroenterology 2010;138:1338-45, 1345.e1-7.
Fukuhara T, Taketomi A, Motomura T, Okano S, Ninomiya A, Abe T, et al.
Variants in IL28B in liver recipients and donors correlate with response to peg-interferon and ribavirin therapy for recurrent hepatitis C. Gastroenterology 2010;139:1577-85, 1585.e1-3.
Chinchai T, Labout J, Noppornpanth S, Theamboonlers A, Haagmans BL, Osterhaus AD, et al.
Comparative study of different methods to genotype hepatitis C virus type 6 variants. J Virol Methods 2003;109:195-201.
Venegas M, Villanueva RA, González K, Brahm J. IL28B polymorphisms associated with therapy response in Chilean chronic hepatitis C patients. World J Gastroenterol 2011;17:3636-9.
Rodriguez-Torres M, Jeffers LJ, Sheikh MY, Rossaro L, Ankoma-Sey V, Hamzeh FM, et al.
Peginterferon alfa-2a and ribavirin in Latino and non-Latino whites with hepatitis C. N
Engl J Med 2009;360:257-67.
Loguercio C, Federico A, Masarone M, Torella R, Blanco Cdel V, Persico M, et al.
The impact of diet on liver fibrosis and on response to interferon therapy in patients with HCV-related chronic hepatitis. Am J Gastroenterol 2008;103:3159-66.
Tohra SK, Taneja S, Ghosh S, Sharma BK, Duseja A, Dhiman RK, et al.
Prediction of sustained virological response to combination therapy with pegylated interferon alfa and ribavirin in patients with genotype 3 chronic hepatitis C. Dig Dis Sci 2011;56:2449-55.
Lonardo A, Adinolfi LE, Loria P, Carulli N, Ruggiero G, Day CP, et al.
Steatosis and hepatitis C virus: Mechanisms and significance for hepatic and extrahepatic disease. Gastroenterology 2004;126:586-97.
Fabris C, Federico E, Soardo G, Falleti E, Pirisi M. Blood lipids of patients with chronic hepatitis: Differences related to viral etiology. Clin Chim Acta 1997;261:159-65.
Tanaka Y, Nishida N, Sugiyama M, Kurosaki M, Matsuura K, Sakamoto N, et al.
Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Nat Genet 2009;41:1105-9.
Mach T, Ciesla A, Sanak M, Glowacki MK, Warunek W, Owczarek D. The importance of IL28B polymorphism in response to pegylated interferon α and ribavirin in chronic hepatitis caused by HCV Genotype 1b. Prz Gastroenterol 2012;7:38-42.
Bugianesi E, Salamone F, Negro F. The interaction of metabolic factors with HCV infection: Does it matter? J Hepatol 2012;56 Suppl 1:S56-65.
Fattovich G, Covolo L, Bibert S, Askarieh G, Lagging M, Clément S, et al.
IL28B polymorphisms, IP-10 and viral load predict virological response to therapy in chronic hepatitis C. Aliment Pharmacol Ther 2011;33:1162-72.
Mangia A, Thompson AJ, Santoro R, Piazzolla V, Tillmann HL, Patel K, et al.
An IL28B polymorphism determines treatment response of hepatitis C virus genotype 2 or 3 patients who do not achieve a rapid virologic response. Gastroenterology 2010;139:821-7, 827.e1.
Falleti E, Bitetto D, Fabris C, Cussigh A, Fornasiere E, Cmet S, et al.
Role of interleukin 28B rs12979860 C/T polymorphism on the histological outcome of chronic hepatitis C: Relationship with gender and viral genotype. J Clin Immunol 2011;31:891-9.
Michael RC, Alexander T, Bart JV, Kym W, Hans T, John JP, et al
. Interleukin-28B Polymorphisms are associated with histological recurrence and treatment response following liver transplantation in patients With hepatitis C virus infection. Hepatology 2010;58:317-24.
Kau A, Vermehren J, Sarrazin C. Treatment predictors of a sustained virologic response in hepatitis B and C. J Hepatol 2008;49:634-51.
Patton HM, Patel K, Behling C, Bylund D, Blatt LM, Vallée M, et al.
The impact of steatosis on disease progression and early and sustained treatment response in chronic hepatitis C patients. J Hepatol 2004;40:484-90.
Di Marco V, Calvaruso V, Grimaudo S, Ferraro D, Pipitone RM, Di Stefano R, et al.
Role of IL-28B and inosine triphosphatase polymorphisms in efficacy and safety of peg-interferon and ribavirin in chronic hepatitis C compensated cirrhosis with and without oesophageal varices. J Viral Hepat 2013;20:113-21.
Poustchi H, Negro F, Hui J, Cua IH, Brandt LR, Kench JG, et al.
Insulin resistance and response to therapy in patients infected with chronic hepatitis C virus genotypes 2 and 3. J Hepatol 2008;48:28-34.
Chowdhury A, Santra A, Chaudhuri S, Dhali GK, Chaudhuri S, Maity SG, et al.
Hepatitis C virus infection in the general population: A community-based study in West Bengal, India. Hepatology 2003;37:802-9.
Zeuzem S, Diago M, Gane E, Reddy KR, Pockros P, Prati D, et al.
Peginterferon alfa-2a (40 kilodaltons) and ribavirin in patients with chronic hepatitis C and normal aminotransferase levels. Gastroenterology 2004;127:1724-32.
Rocco A, Compare D, Coccoli P, Esposito C, Di Spirito A, Barbato A, et al.
Vitamin B12 supplementation improves rates of sustained viral response in patients chronically infected with hepatitis C virus. Gut 2013;62:766-73.
Iqbal S, Khalil-Ur-Rahman, Sheikh MA, Arshad M. Response of different HCV genotypes to interferon therapy in different age groups of chronic hepatitis-C patients. J Ayub Med Coll Abbottabad 2014;26:310-5.
Adinolfi LE, Gambardella M, Andreana A, Tripodi MF, Utili R, Ruggiero G, et al.
Steatosis accelerates the progression of liver damage of chronic hepatitis C patients and correlates with specific HCV genotype and visceral obesity. Hepatology 2001;33:1358-64.
Hsu CS, Liu CH, Liu CJ, Wang CC, Chen CL, Lai MY, et al.
Association of lipid profiles with hepatitis C viral load in chronic hepatitis C patients with genotype 1 or 2 infection. Am J Gastroenterol 2009;104:598-604.
Rubbia-Brandt L, Fabris P, Paganin S, Leandro G, Male PJ, Giostra E, et al.
Steatosis affects chronic hepatitis C progression in a genotype specific way. Gut 2004;53:406-12.
Liu P, Li Y, Sun C. Correlations of serum hepatitis C virus RNA and alanine transaminase with liver histopathological changes in patients with chronic hepatitis C. Lab Med 2009;40:167-9.
Prof. Showkat Ali Zargar
Department of Gastroenterology, Sher-I-Kashmir Institute of Medical Sciences, Soura, Srinagar - 190 011, Jammu and Kashmir
Source of Support: None, Conflict of Interest: None
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]