Manuscript accepted on :May 23, 2017
Published online on: --
Plagiarism Check: Yes
Shahrzad Nokhbeh Zaeem
Islamic Azad University of parand, Parand, Iran.
Corresponding Author E-mail: shahezad.nz@gmail.com
DOI : https://dx.doi.org/10.13005/bpj/1264
Abstract
Hepatitis B Vs in most cases appears to chronic liver inflammation and liver in the long term can lead to cirrhosis or cancer. Attempts have been made to treat and control the disease as a major health problem in the world and is considered done. Recent studies on the biology of the virus cause diagnostic markers including hepatitis B virus genotypes Vs and seeking nuclear gene has been mutated strains. On the other hand the distribution of genotypes of the virus in different countries and the relationship between genotype and different serotypes in the world. Determine the different types of hepatitis genotype should be determined in each country of the region, such as determining the therapeutic protocol to implement antiviral therapy based on genotype will be different. In this study published papers related to the prevalence of hepatitis B virus genotypes and cultivars Vs mutant genotypes were searched. The results show that in patients with hepatitis B genotype dominant form in Asia C In northern and central Europe genotype A, in the countries around the Mediterranean and East Europe genotype D in Latin America genotype H and F, Genotypes in Africa a and E In patients with genotype 1 Hepatitis C virus. Also, in the United States and northern Europe, genotype 2 in sub-Saharan Africa and Central and West Africa and South-East Asia, genotype 3 in sub-Saharan Africa and the Far East and the Indian subcontinent, genotype 4 in the Middle east and Africa, genotype 5 in south Africa and genotype 6 in south China and south east Asia are high. Cirrhosis of the liverin genotype 1 and 4 are more common. With the arrival of protease inhibitors of Hepatitis C virus in the field of treatment and drug resistance observed in these types of treatments, studied the genome of hepatitis C in the presence of mutations associated with resistance to protease inhibitors has become important. In hepatitis C from the marker gene polymorphisms I LB 28 and genotype, gene polymorphisms ITPA to identify mutations associated with resistance to inhibitors are used.
Keywords
epidemiology; genotype; Hepatitis B Vs;molecular markers;
Download this article as:Copy the following to cite this article: Zaeem S. N. Epidemiology of Hepatitis B Virus Genetic Diversity Vs and Diagnostic Molecular Markers of Hepatitis C Virus Core Gene. Biomed Pharmacol J 2017;10(3). |
Copy the following to cite this URL: Zaeem S. N. Epidemiology of Hepatitis B Virus Genetic Diversity Vs and Diagnostic Molecular Markers of Hepatitis C Virus Core Gene. Biomed Pharmacol J 2017;10(3). Available from: http://biomedpharmajournal.org/?p=15817 |
Introduction
Hepatitis 10 or 15 years ago were identified. Management of hepatitis viruses has changed since the early nineties. Today, the proliferation of hepatitis B and C can be a powerful anti-virus suppressed. Many new antiviral drugs, especially Protease polymerase inhibitors, are currently under development. Hepatitis B virus genotypes and response to treatment of chronic hepatitis C is one of the most important criteria are considered as well as the distribution of genotypes of the virus in certain communities is different.
Determine the distribution of different genotypes of hepatitis B Vs must be determined in each country of the region, such as determining the therapeutic protocol to implement antiviral therapy based on genotype will be different. Hepatitis C genotype by diagnostic markers including search and core genes can be mutated strains of hepatitis C genotype determined resistance to the drug. [2001.1, Simmonds et al]
Hepatitis B Virus Genotypes
10 genotypes of hepatitis B virus (A-J), various types of different serotypes (ayr, adw, adr ayw) Is the distribution of genotypes of the virus in different countries and the relationship between genotype and different serotypes in the world. [2, 2014 Pourkarim et al]
Epidemiology of Hepatitis B Virus
Worldwide prevalence of hepatitis B virus has a wide range. In 12% of the population, including West Europe, USA, Canada, Australia and New Zealand show a lower prevalence of hepatitis B virus. In these areas, Risk of infection is less than 20%. About 43 percent of the world population, including the Mediterranean countries, Japan, Central Asia, Middle East, South America and Latin shows the average prevalence of hepatitis B virus. In more than 60% of the world’s population, South East Asia, China and sub-Saharan Africa shows a high prevalence of hepatitis B virus] Wasley et al [4, 1975, Stevens et al
3, 2008]. Iran Hepatitis B is an average areas booklet. In Iran, 35% of people with the virus have an average of 3% (approximately 2/000/000) are carriers of the virus, but the rate of prevalence in different provinces, for example, Sistan and Baluchestan differ by more than 5% arrives. In high prevalence areas where the standard of living is lower and where the socio-economic standard is lower, more disease have been reported. The difference in the prevalence of the disease in different parts of the world is probably age-related diseases. [Haghshenas et al, 2014, 5]
According to the vaccination of infants and high-risk individuals, the prevalence percentage (and number) diseases in the world has decreased. The prevalence of chronic hepatitis B In different parts of the world is different from the direction of the three Logic prevalence of high, medium and low yields are areas with low prevalence, including the US, Western Europe, Australia and New Zealand that 1 to 2 percent of the population are chronic carriers of hepatitis B Respectively. Areas with intermediate prevalence, including the countries of the Mediterranean area, Japan, India,
Singapore, Middle East, South America and Latin 3 to 5 percent of the population carries hepatitis B Respectively.
Regions with high style, Southeast Asia and Africa, 10 to 7% of the population are chronic carriers of hepatitis B Respectively.
Africa
African countries have the highest rates of hepatitis B virus. Research with several countries Including Ivory Coast, Ghana, Cameroon and Uganda took place showed high genetic diversity in the genotype of the virus. Prevailing in the country genotypes Genotype A and E have been reported. Genotype A With serotypes A1, A2 and A3 is that all serotypes A It is in these countries. Genotype E Have different serotypes, of which serotype ayw4 and adw2 the highest frequency among patients, respectively [6, 2013 Joseph et al].
Latin America
Latin American countries have average rates of infection are hepatitis B virus. Among the features of different Latin American countries, the genotype of the virus. Hepatitis B virus genotypes in Latin America, including Mexico Type H and in Central America of F is. Liver cancer is rare in Mexico, but the relationship between liver cancers with serotype Fb 1 has been found in Argentina. This shows the importance of ensuring that genetic and environmental factors in the development of liver disease associated with hepatitis B virus in Latin America., [Roman e t al, 2014, 7]
Asia
Southeast and East Asia, with 25 percent of the world’s population with the highest rates of infectious diseases. The prevalence of hepatitis B virus in a wide range of areas. Genotypes that appeared in this logic are: A, B, C, D. In Asian countries such as Korea, Japan, Taiwan and China often, chronic hepatitis B is transmitted from infected mothers to babies. The predominant genotype in South Korea C Is that the rate of mortality from liver diseases in this country is relatively high. [Hyun Bae et al, 2005, 8]
China, Asia’s most populous country with the highest immigrant populations is therefore different genotypes of hepatitis B virus is distributed in this region. The most common genotypes, respectively. B and C High rates of genotype C in China due to rapid adaptation of the virus with the host environment. Liver disease caused by infection with genotypes C There were periods are more aggressive disease. [9, 2011, Chan]
Now Iran is among the areas with low prevalence. In 1980, the prevalence of hepatitis B in Iran about 3%, but in recent decades the prevalence significantly reduced where responsibility can be public awareness about risk factors, the vaccination of 1993 for all newborns and people with risk high, such as health care workers and use of disposable syringes named. The main route of transmission from mother to infant and injecting drug users is and 56-51 percent of Iranian patients with cirrhosis of HBsAg Are positive. Genotypes in Iran D And subtype ayw2 is dominant and approximately 80% of patients with chronic hepatitis B in Iran HBeAg Negative [Haghshenas et al, 2014, 5].
Europe
Genotype in North and Central Europe A While more common in the countries around the Mediterranean and East Europe, the genotype D Sunburn appear in patients with genotype G Germany, the Netherlands and Georgia were diagnosed. [Schaefer et al, 2007, 10][Van der Kuy e t al, 2011, 12] [Vieth et al, 2002, 11]
Hepatitis C Genotype
Based on the differences in the genome, hepatitis C virus genotypes and subtypes are different. Hepatitis C with genotype 6 (6 5-4-3-2-1) and more than 100 subtypes that genotypes 1 and 4 of its global expansion and genotypes 5 and 6 specific areas of the world are seen. Determine the different types of hepatitis genotype should be determined in each country of the region. When determining treatment protocols to implement antiviral therapy based on genotype will be different. Iran conducted studies in order to identify the genotype of each specific objective pursued and on certain groups of society often have done. 13, 2014, Gower et al]
Epidemiology of Hepatitis
Hepatitis C prevalence in different parts of the world there is a wide range. In some countries such as Egypt prevalence (> 10%) [14, 2013, WHO]. In West Africa, the Pacific and its prevalence is significantly higher than North America and Europe. It is estimated that 2 to 5 million patients with hepatitis C virus exist in Europe. The prevalence of hepatitis C virus antibodies in healthy blood donors US (1/6%), Italy (1/15%), Germany (0/4%) and Scandinavia (0/23%) [15, Hatzakis et al 2011]. In Europe and the US have chronic hepatitis C, the most common cause of cirrhosis, liver diseases and hepatomegaly cell carcinoma is the most important reason for liver transplantation. 16, 2009, Vogel et al]
The rate of infection in Iran is about 1% of the population. Hepatitis C virus genotypes significant differences in nucleotide and amino acid sequences themselves, which leads to differences in biological activity and thus viral pathogenesis can be caused by any of these genotypes. Among the most important differences in the genotype are considered physicians is significant difference between treatment response in patients with genotype 1 compared with patients with genotype 3 is, as in treatment with a combination of interferon alpha Pegylated and sustained viral response ribavirin in patients with genotype 1 patients with genotype 3 between 40 and 50 and between 70 and 80 percent. The prevalence of hepatitis C virus genotypes vary according to geographic locations: genotype 1 hepatitis C worldwide, including developed areas like North America and Europe can be found. Hepatitis C virus genotype 2 virus has spread in Central and West Africa and South East Asia as well as some Western countries, while genotype 3 hepatitis C, mainly in the Far East and the Indian subcontinent has been found [17, 2004 Simmonds]. Meanwhile, figures genotype 4, 5 and 6 of hepatitis C. Native particular geographic areas are as follows: genotype 4 hepatitis C, mainly in Egypt and sub-Saharan Africa, genotype 5 Hepatitis C in South Africa, 2010, [Antaki et al 18], and hepatitis C genotype 6 is found in southern China and South East Asian countries there. [Mellor et al, 1995, 19] [Alter, 2007, 20]
Genotype 1
Genotype 1 is the most common type of hepatitis C worldwide, especially in the United States and Northern Europe, which is about 70 percent sufferer’s hepatitis C Chronic in the world [Hnatyszyn et al, 2005, 21]. Genotype 1 is the most common type of hepatitis C worldwide, the predominant subtypes a 1 b 1. Subtypes b 1 is transmitted through blood.
In addition, genotype 1 ratio to treatment with interferon-alpha / ribavirin were resistant. Increase response rates stable emergence of viral drug resistance is a concern that may affect the result of new treatments. [Sarrazin et al, 2012, 22]
Genotype 2
Hepatitis C genotype 2 for sub-Saharan Africa and South East Asia, [Sulbaran et al, 2010, 23]. In some European countries such as the Netherlands and France 2 hepatitis C genotype is more prevalent among immigrant populations. [van de Laar et al, 2006, 24]
Genotype 3
Research in Africa represent different genotypes on the continent. In Central and West Africa genotype 2 and genotype 3 hepatitis C has been developed South Africa. Hepatitis C genotype 3 in the first was established in South Africa to the Far East and the Indian subcontinent immigrants then moved [Abid et al, 2000, 25]. The researchers found a significant association between genotype 3 hepatitis C fibrosis and progression of fibrosis by increasing the speed of getting there. These observations may have important implications for the management of patients infected with the genotype. Subtypes a 3 is found mainly among intravenous drug users. [Bochud et al, 2009, 26]
Genotype 4
Genotype 4 hepatitis C in the Middle East and Africa, is common in Egypt prevalence is extremely high, the prevalence of ultra-high causing an increasing incidence of hepatocellular carcinoma in Egypt, which is currently the second leading cause of cancer mortality cancer among men in this country. The genotypes resistant to existing treatments. [el-Zayadi et al, 2005, 27]
Genotype 5
40% of patients with hepatitis C genotype 5 in South Africa, but sporadic cases in four countries: France, Spain, Syria and Belgium have been found. [Antaki et al, 2010, 28]
Genotype 6
6 genotypes of hepatitis C in southern China and South-East Asia is limited, and sometimes among immigrants
Native countries can be found. Among the countries with high prevalence of genotype 6 than other genotypes include Vietnam, Thailand, Laos. Patients with this genotype most responsive to treatment than genotypes 3 Mybashnd.myzan injecting drug users, but higher than genotype 1. [Pham et al, 2009, 29][ Yan et al, 2009, 30][Pybus et al 2012, 31]
Hepatitis C Diagnostic Molecular Markers
Recent studies on the biology of the virus, including genotypes of hepatitis C cause diagnostic markers, and search for the core gene is mutated strains. With the arrival of protease inhibitor drugs to treat hepatitis B virus into Vs and observed drug resistance to these therapies, the hepatitis B virus genome Vs investigated for the presence of mutations associated with resistance to protease inhibitors has become important.
Gene Polymorphisms Ilb 28
Gene ILB 28 protein gene IFN λ 3 which has an important role in the innate immune response to Hepatitis C virus infection. In the intermediate genes ILB 28 ILA 28 Number of genetic polymorphisms that are the most important ones polymorphisms rs12979860 and rs8099917. In patients with the favorable genotype of these polymorphisms, ie,
rs12979860 CC and rs8099917 TT rates of spontaneous viral clearance and response to interferon combination therapy containing a significant increase compared to unfavorable genotypes of these polymorphisms, ie, rs12979860 TT and rs8099917 GG. The effect of this polymorphism on spontaneous viral clearance and response to treatment in patients infected with genotype 1-infected patients has been demonstrated, but in genotype 3 is located in the cool of ambiguity. Finally, it can be concluded IL28B One of the most powerful predictor of treatment response in patients infected with genotype 1 prior to treatment is and now it can be used as a prognostic factor in the treatment of Hepatitis C virus. [Domagalski et al, 2013, 32] [Amol et al, 2013, 33]
Genotype, Gene Polymorphisms ITPA
Dual therapy with ribavirin and interferon in some patients with adverse events such as anemia. This condition is one of the most important factors lowering the dose of ribavirin and reduce to pass your feet of virus Will cost. One of the genetic factors influencing the use of ribavirin and interferon anemia, gene polymorphisms
ITPA In particular polymorphism rs1127354 and rs7270101. Variants of these polymorphisms are associated with a decrease in protein activity ITPase As a result, resistance against anemia associated with ribavirin, respectively. Knowing the genotype of these polymorphisms are of anemia during treatment with ribavirin and for measures such as the use of erythropoietin predicted taken into account. [Aghemo et al, 2014, 34][Jyh Hwang et al, 2015, 35]
Resistance to Protease Inhibitors
In recent years, the supply of drugs, including protease inhibitors and Boceprevir and Telaprevir, hepatitis C treatment changed. While treatment with these drugs with a call lasting more virus than the usual treatment in combination with interferon-alpha pegylated and ribavirin is the use of these drugs may be associated with the emergence of variants resistant to the treatment of virus that use restrictions protease inhibitors is. Protease inhibitors inhibit serine protease encoded by genes NS 3 Virus replication of hepatitis C inhibit and if variants containing mutations of resistance to these drugs in the treatment chosen viral load increases and therapy needed to clear the virus will not be, the result could be over treatment sequence analysis NS 3 Hepatitis C in the presence of resistant variants to investigate and, if necessary, to better manage patient [Fatima et al, 2014, 36].
Result
The results show that in patients with hepatitis B genotype dominant form in Asia C In northern and Central Europe genotype A, in the countries around the Mediterranean and East Europe genotype D in Latin America genotype H and F, Genotypes in Africa A and E In patients with genotype 1 Hepatitis C virus. Also, in the United States and northern Europe, genotype 2 in sub-Saharan Africa and Central and West Africa and South East Asia, Far East genotype 3 in sub-Saharan Africa and the Indian subcontinent, genotype 4 in the Middle east and Africa, genotype 5 in south Africa and genotype 6 in south China and south east Asia are high. Cirrhosis of the liver in genotype 1 and 4 are more common. With the arrival of protease inhibitor drugs to treat hepatitis B virus into Vs and observed drug resistance to these therapies, investigate hepatitis C viral genome for the presence of mutations associated with resistance to protease inhibitors has become important. In hepatitis C from the marker gene polymorphisms IL28B and genotype, gene polymorphisms ITPA to identify mutations associated with resistance to inhibitors are used.
Acknowledgement
This research was supported by Islamic Azad university of Parand. We are thankful to our colleagues who provided expertise that greatly assisted the research.
Reference
- Simmonds P. The origin and evolution of hepatitis viruses in humans. J Gen Virol. 2001;(4):693-712.
CrossRef - Pourkarim M. R., Amini-Bavil-Olyaee S., Kurbanov F., Ranst M. V., Tacke F. Molecular identification of hepatitis B virus genotypes subgenotypes: Revised classification hurdles and updated resolutions. World J Gastroenterol. 21;2014; 20(23):7152–7168.
- Wasley A., Grytdal S., Gallagher K. Centers for Disease Control and Prevention (CDC).Surveillance for acute viral hepatitis United States. MMWR Surveill Summ. 2008;(57):1-24.
- Stevens C. E., Beasley R. P., Tsui J., Lee W. C. Vertical transmission of hepatitis B antigen inTaiwan. N Engl J Med. 1975;(292):771-4.
CrossRef - Haghshenas M. R., Arabi M., Mousavi T. Hepatitis B Genotypes in Iran .Mater Sociomed. 2014;(2):129–133.
CrossRef - Forbi J. C., Ben-Ayed Y., Guo-liang X., Vaughan G., Drobeniuc J., William M. S and Yury E. Khudyakov. Disparate distribution of hepatitis B virus genotypes in four sub-Saharan African countries. J Clin Virol. 2013;58(1):59–66. doi:10.1016/j.jcv.2013.06.028.
CrossRef - Roman S., Jose-Abrego A., Alma Fierro N., Escobedo-Melendez G., Ojeda- Granados C., Martinez-Lopez E., Panduro A. Hepatitis B virus infection in Latin America: A genomic medicine approach”. WJG 20th Anniversary Special Issues (9): Hepatitis B virus. World J Gastroenterol. 2014;21;20(23):7181–7196.
- Bae S. H., Yoon S. K ., Jang J. W., Kim C. W., Nam S. W., Choi J. Y., Kim B. S., Park Y. M., Suzuki S., Sugauchi F., Mizokami M. Hepatitis B Virus Genotype C Prevails Among Chronic Carriers of the Virus in Korea. J Korean Med Sci. 2005;20:816-20. ISSN 1011-8934.
- Chan H. L. Significance of hepatitis B virus genotypes and mutations in the development of hepatocellular carcinoma in Asia. J Gastroenterol Hepatol. 2011;26:8–12.
CrossRef - Schaefer S. Hepatitis B virus genotypes in Europe. Hepatol Res: Offic J Jpn Soc Hepatol. 2007;37(s1):S20–6.
CrossRef - Vieth S., Manegold C., Drosten C., Nippraschk T., Gunther S. Sequence and phylogenetic analysis of hepatitis B virus genotype G isolated in Germany Virus Genes. 2002;24(2):153–6.
- van der Kuy A. C., Zorgdrager F., Hogema B., Bakker M., Jurriaans S., Back N. K., et al. High prevalence of hepatitis B virus dual infection with genotypes A and G in HIV-1 infected men in Amsterdam, the Netherlands, during2000–2011. BMC Infect Dis. 2013;13:540.
CrossRef - Gower E., Estes C., Blach S., Razavi-Shearer K., Razavi H. Global epidemiology and genotype distribution of the hepatitis C virus infection. J Hepatol. 2014;61:S45–S57.
CrossRef - Who. World Health Organization. 2003. “HepatitisC”.www.who.int/csr/disease/hepatitis/Hepc.pdf
- Hatzakis A., Wait S., Bruix J., Buti M., Carballo M., Cavaleri M., Colombo M., Delarocque-Astagneau E., Dusheiko G., Esmat G., Esteban R., Goldberg D., Gore C., Lok A. S., Manns M., Marcellin P., Papatheodoridis G., Peterle A., Prati D., Piorkowsky N., Rizzetto M., Roudot-Thoraval .F, Soriano V., Thomas H.C., Thursz M., Valla D., van Damme P., Veldhuijzen I. K., Wedemeyer H., Wiessing L., Zanetti A. R., Janssen H. L. The state of hepatitis B and C in Europe: report from the hepatitis B and C summit conference. J Viral Hepat. 2011;(1):1-16.
- Vogel M., Deterding K., Wiegand J., Grüner N. H., Baumgarten A., Jung M. C., Manns M. P., Wedemeyer H., Rockstroh J. K. Initial presentation of acute hepatitis C virus (HCV) infection among HIV-negative and HIV-positive individuals-experience from 2 large German networks on the study of acute HCV infection. Clin Infect Dis. 2009;(49):317-9.
CrossRef - Simmonds P. Genetic diversity and evolution of hepatitis C virus–15 years on. J Gen Virol. 2004;85:3173–3188.
CrossRef - Antaki N., Craxi A., Kamal S., Moucari R., Van der Merwe S., Haffar S., Gadano A., Zein N., Lai C. L., Pawlotsky J. M., et al. The neglected hepatitis C virus genotypes 4, 5 and 6: an international consensus report. Liver Int. 2010;30:342–355.
CrossRef - Mellor J., Holmes E. C., Jarvis L. M., Yap P. L., Simmonds P. Investigation of the pattern of hepatitis C virus sequence diversity in different geographical regions: implications for virus classification. The International HCV Collaborative Study Group. J Gen Virol. 1995;76(10):2493–2507.
CrossRef - Alter M. J. Epidemiology of hepatitis C virus infection. World J Gastroenterol. 2007;13:2436–2441.
CrossRef - Hnatyszyn H. J. Chronic hepatitis C and genotyping: the clinical significance of determining HCV genotypes. Antivir Ther. 2005;10:1–11.
- Sarrazin C., Hezode C., Zeuzem S., Pawlotsky J. M. Antiviral strategies in hepatitis C virus infection. J Hepatol. 2012;56(1):S88–S100.
CrossRef - Sulbarán M. Z., et al. 2010. “ Genetic history of hepatitis C virus in Venezuela: high diversity and long time evolution of HCV genotype 2”. PLoS One 5:e14315 doi:10.1371/journal.pone.0014315. 24.
CrossRef - van de Laar T. J., et al. Diversity and origin of hepatitis C virus infections among unpaid blood donors in the Netherlands. Transfusion. 2006;46:1719–1728.
CrossRef - Abid K., Quadri R., Veuthey A. L., Hadengue A & Negro F. A novel hepatitis C virus (HCV) subtype from Somalia and its classification into HCV clade 3. J Gen Virol. 2000;81:1485–1493.
CrossRef - Bochud P. Y., Cai T., Overbeck K., Bochud M., Dufour J. F., Mullhaupt B., Borovicka J., Heim M., Moradpour D & other authors Genotype 3 is associated with accelerated fibrosis progression in chronic hepatitis C. J Hepatol. 2009;51:655–666.
CrossRef - el-Zayadi A. R., Badran H. M., Barakat E. M., Attia Mel-D., Shawky S., Mohamed M. K., et al. Hepatocellular carcinoma in Egypt: a single center study over a decade. World J Gastroenterol. 2005;11(33):5193–5198.
- Antaki N., Craxi A., Kamal S., Moucari R., Van der Merwe S., Haffar S., Gadano A., Zein N., Lai C. L., Pawlotsky J. M., Heathcote E. J., Dusheiko G., Marcellin P. The neglected hepatitis C virus genotypes 4, 5 and 6: an international consensus report. Liver Int. 2010;30(3):342-55. doi: 10.1111.
- Pham D. A., Leuangwutiwong P., Jittmittraphap A., Luplertlop N., Bach H. K., Akkarathamrongsin S., Theamboonlers A., Poovorawan Y. High prevalence of Hepatitis C virus genotype 6 in Vietnam. Asian Pac J Allergy Immunol. 2009;27:153–160.
- Pybus O. G., Barnes E., Taggart R., Lemey P., Markov P. V., Rasachak B., Syhavong B., Phetsouvanah R., Sheridan I., Humphreys I. S., et al. Genetic history of hepatitis C virus in East Asia. J Virol. 2009;83:1071–1082.
CrossRef - Yan Z., Fan K., Wang Y., Fan Y., Tan Z., Deng G. Changing pattern of clinical epidemiology on hepatitis C virus infection in southwest china.Hepat Mon. 2012;12:196–204.
CrossRef - Domagalski K., Pawlowska M., Tretyn A., Halota W., Pilarczyk M., Smukalska E., Linkowska K., Grzybowski T. Impact of IL-28B polymorphisms on pegylated interferon plus ribavirin treatment response in children and adolescents infected with HCV genotypes 1 and 4. Eur J Clin Microbiol Infect Dis. 2013;32(6):745–754.
CrossRef - Amol S. Rangnekar and Robert J. Fontana. IL-28B polymorphisms and the response to antiviral therapy in HCV genotype 2 and 3 varies by ethnicity a meta-analysis. J Viral Hepat. 2013;20(6):377–384.
CrossRef - Aghemo A., Grassi E., Rumi M. G., D’Ambrosio R., Galmozzi E., Degasperi E., Castaldi D., Soffredini R., Colombo M. Limited Utility of ITPA Deficiency to Predict Early Anemia in HCV Patients with Advanced Fibrosis Receiving Telaprevir. PLoS One. 2014;9(4):e95881.
CrossRef - Hwang J. J.,Lo C. H. C., Lin C. H. H., Cheng H. S., Hung I. W., Tsai W. J., Hung C. H. H. Association between IPTA Gene Polymorphisms and Hematological Abnormalities in Hepatitis C Virus-Infected Patients Receiving Combination Therapy. Gut Liver. 2015;9(2):214–223. 36.
- Fatima K., Azhar E., Mathew S. H., Damanhouri G. H., Qadri I. Comparison of Structural Architecture of HCV NS3 Genotype 1 versus Pakistani Genotype 3a. Biomed Res Int. 2014:749254.
CrossRef - Naybin M. Y. Study on the relationship between hepatitis C virus and hepatitis B virus blood level and plasma protein profile. Thesis Submitted for the degree Master of Science. 2015.