Skip to main content

Hepatitis C virus genotypes in Saudi Arabia: a future prediction and laboratory profile

Abstract

Background

Hepatitis C virus (HCV) genotypes and subtypes are considered an important tool for epidemiological and clinical studies and valuable markers for disease progression and response to antiviral therapy. The aim of this study was to identify the prevalence of HCV genotypes and their relation to socio-demographic factors particularly age and sex, various biochemical profiles and viral load.

Methods

The records (630) of Saudi patients positive for HCV (2007–2011) reported in the system of the Molecular Pathology Laboratory at a tertiary reference hospital in Riyadh, Saudi Arabia were analyzed. Socio-demographic characteristics, liver biochemical profile, viral load and co-infection with HBV and HIV were retrieved from the hospital database. The associations of continuous and categorical variables with genotypes were analyzed.

Result

The overall mean age of the surveyed patients was 59 years ±0.5 years (21% were <50 years (p = 0.02). The rate of infection is lower in males than in females (47.6% vs. 52.4%).

HCV genotype 4 was the most prevalent (60.7%), followed by genotype 1 (24.8%). However, genotype 1 and 3 were found more in males (29.7% vs. 20.3% and 6% vs. 2.1%, respectively, p = 0.001), while genotype 2 and 4 were more among females (4.8% vs. 2% and 68.5% vs. 52.3%, respectively). In addition, genotype 1 was found dominant in younger males (33.8%).

Biochemical parameters across gender showed significant variation in particular for the ALT (p = 0.007). The mean viral load was significantly higher in genotype 1 than genotype 4 (4,757,532 vs. 1,435,012, p = <001). There is a very low overall percentage of co-infection of HBV or HIV in this study (around 2% for each).

Conclusion

Although HCV genotype 4 shows an overall high prevalence in this study, a clear decline in the rate of this genotype was also demonstrated in particular among the younger age group who displayed increasing trends toward the global trend of genotype 1, rather than genotype 4. This finding would be of clinical interest in relation to future planning of the therapy for HCV infected patient.

Background

Hepatitis C virus (HCV) is a positive-strand RNA virus of the genus Hepacivirus within the Flaviviridae family infection [1]. It is a well-known causative agent of a serious, contagious, and inflammatory disease, which affects the normal function of the liver, predominantly as chronic infection [2, 3]. The global pattern of this infection is on the increase despite the improvement in transfusion practices and general health measures directed to limit the transmission of this disease [4].

Most studies have indicated that HCV is an endemic medical condition, and numerous steps are followed to eliminate the risk of this infection. Nonetheless the distributions of the variables of the viral infection such as genotype, age, and race across the world are on the increase despite the availability and efficacy of the HCV therapy [5, 6].

Indeed, various epidemiological studies have presented evidence indicating that the high incidence rate of HCV infection is a major threat for the population [5], and reports on the prevalence of HCV in Saudi Arabia are still inconsistent between different studies with wide variations in their target population. Although the prevalence of HCV was found to be around 50% among infected hemodialysis patients, the prevalence rates of 0.4–1.1% could be accepted among the general population based on data from blood donor screening centers [7,8,9].

On the other hand, the most prevalent genotype in Saudi Arabia is genotype 4, which is often followed by the genotype 1 [10,11,12,13,14,15,16,17,18,19,20,21,22,23]. These two genotypes are not only difficult to treat, but also are highly pathogenic. Most of these early studies in Saudi Arabia barely discussed the relation between the genotypes and age of the affected individuals. For example, the incidence of the infection was found to be high among the old people (>50 years) indicating past infection [24]. In most of those early publications the dominant genotype was genotype 4. This raised the question, whether the same genotype is currently prevalent in the younger Saudi generations? Also, could we predict the future genotype based on the currently available genotype analysis, in Saudi Arabia? Thus, the rationale behind conducting this study is to assess the relationship between HCV genotypes and certain epidemiologic and biologic features of HCV infected patients. Accordingly, the aim of this study was to find answers to these questions and also to correlate the HCV genotypes with the biochemical profiles and viral load. The study also aims to describe the prevalence of HCV genotypes based on socio-demographic factors (particularly age and sex) and to identify HCV genotypes with co-infection with HBV and HIV.

Methods

Participants and samples

A total of 630 Saudi patients were studied at a tertiary reference hospital in Riyadh, Saudi Arabia (King Abdulaziz Medical City). They were confirmed as HCV positive with the HCV-RNA genotype amplification polymerase chain reaction (PCR) method in the period from 2007 to 2011. HCV genotype results were retrieved from the Molecular Pathology Laboratory (MPL) database with additional information related to socio-demographic characteristics, and liver biochemical profile. The viral load (IU/ml) of the diagnosed patients was also retrieved from the Laboratory Information System (LIS) and QuadraMed Clinical Pathology Record (QCPR) system. Patients with incomplete HCV genotype results were excluded.

The recorded variables included: age, sex, clinical diagnosis, genotype, and biochemical profile, mainly alanine transaminase (ALT), aspartate aminotransaminase (AST), alkaline phosphates (ALP) and total serum bilirubin measures. Other variables related to the HCV characteristics were recorded, including viral load [reported in international units per milliliter (IU/mL) and copies per milliliter] and co-infection with HBV or HIV.

Statistical analysis

The results are expressed as means ± standard deviations or as percentages. The means between groups were compared by using the student t test. The frequency distributions of the different genotypes within age groups and proportion were used. The associations between categorical variables were assessed using the Chi Square and Fisher’s exact tests. Statistical analysis was performed using SPSS 20.0 software (SPSS Inc., USA) and P values of 0.05 or less were considered significant.

No informed consent was needed since the analyzed laboratory data was secondary (without names or identity). Nonetheless, this study was reviewed and approved by the internal Institutional Review Board (IRB) in the College of Public Health and Health Informatics (CPHHI), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) and King Abdullah International Medical Research Center (KAIMRC) under # SP 14/053.

Results

Demographic characteristics (Table 1 and Table 2)

Socio-demographic factors of the patients’ positive for HCV genotypes are presented in Table 1. The mean age of the studied population was 59 years ±0.5 years. However, of the 630 recruited patients, 132 (21%) were below 50 years, and more than half (56.0%) were in the age group 50–69 years; the difference between the age groups is significant (p = 0.02). The rate of infection in male is lower than in females (47.6% vs. 52.4%, p = 0.02).

Table 1 Demographic Characteristics of the Study Group
Table 2 Distribution of genotype tests over a five year period (2007–2011)

The number of HCV infected cases increased gradually over the period of 5 years (2007–2011) (Table 2). The highest reported rate was in the year 2010 (31.6%) and the lowest in the year 2008 (6.2%), but the annual infection rate remained almost unchanged (p = 0.409).

Distribution of genotypes according to gender and age (Table 3)

The overall distribution of the genotypes showed predominance of genotype 4 (60.7%) followed by genotype 1 (24.8%) including subtypes (a) and (b); for other genotypes the rate ranged between 3.5% for genotypes 2, 3 and mixed genotypes (3.5%, 4.1% and 7%, respectively). On the other hand, the genotype distribution varied significantly by gender (P < 0.001) as genotype 1 and 3 were more predominant in males, compared to females (29.7% vs. 20.3% and 6% vs. 2.1%, respectively, P = 0.001), while genotypes 2 and 4 were more predominant in females than in males (4.8% vs. 2% and 68.5% vs. 52.3%, respectively).

Table 3 The HCV genotype and subtype distribution are related to the genders

When comparing genotype 1 and 4 by age groups among the males and females, the overall rate of genotype 1 was higher among males than in females (30% vs. 20%, respectively, P < 0.001). Although a limited number of males was noted at the age group <50 years (74/300) with hepatitis C virus genotypes, 33.8% of them were males with genotype 1 infection, in comparison to females in the same age group (58/330, P < 0.001) seen with genotype 1 infection (20.7%). In contrast, genotype 4 was the predominant genotype among elder females (50–69 and ≥70 years) than among males of the same age groups (67% and 68%, vs 54% and 53%, respectively, P = 0.539). No significant differences were found in age between genotypes 1 or 4 (Fig. 1).

Fig. 1
figure 1

Genotypes distribution by age groups and gender

Biochemical profile (Table 4 and Table 5)

Table 4 shows a statistically significant variation in the mean value of the biochemical parameters across gender of some biochemical parameters, in particular the ALT (P = 0.007); similar trend was also noted for the viral load (P < 0.001). No significant differences were found between gender with respect to the biochemical parameters such as AST, ALP and total serum bilirubin.

Table 4 Biochemical profile of the study group
Table 5 HCV Genotype one and four Distribution across Biochemical Profile (630)

When focusing on the main issue of the current study, i.e. genotype 4 and genotype 1, the findings of the viral load showed significantly higher mean viral load in genotype 1 than genotype 4 (4,757,532 IU/ml vs. 1,435,012 IU/ml, P = <001). The rest of the tests showed no significant difference between genotype 1 and 4 (Table 5). As to the co-infection of HCV with either HBV or HIV, no significant relation could be established. Besides there is a very low overall percentage of co-infection in this study (around 2% for each).

Predictive factor analysis was conducted for genotype 1 using univariate and multivariate logistic analysis, considering genotype 4 as reference. The unadjusted odds of genotype 1 increased by 85.5% in males, 80% among patients with moderate viremia, 3 times more in patients with high viremia, and 90.7% among patients with high AST. However the odds decreased by 41.4% in patients with high ALT. According to the multivariate logistic regression analysis, the adjusted odds for genotype 1 showed an increase by 69.7% in males, 83.6% of patients with moderate viremia, and increased 3 times in patients with high viremia (Table 6).

Table 6 Univariate and multivariate analysis of gender, age, and biochemical profile in reference to genotypes 1 and 4a

Discussion

Hepatitis C virus is one of the most enduring causes of viral hepatitis, and numerous studies found strong connection between hepatitis C infection and various other infections, co-morbidities, and increased mortality rates [25].

The present study on the genotypes of 630 hepatitis C infected patients revealed that genotype 4 was confirmed in the majority of these patients (60.8%). This finding confirms previous reports where genotype 4 is a landmark of the infected cases of HCV in Saudi Arabia [7, 17, 18]. Besides, many review articles that described the global distribution of HCV genotypes [11, 23, 26, 27], defined clearly that genotype 4 is the dominant genotype in Middle Eastern countries, particularly Saudi Arabia, Egypt, Jordan, Yemen, Oman, and Sudan [11,12,13, 28]. We also found that genotype 4 was found in higher rate among females than males, but the different was not statistically significant, and this is in line with a similar earlier study in the Kingdom of Saudi Arabia (KSA) [12].

Age and past exposure

In the present study 79% of HCV cases were above 50 years old, indicating that the majority of these cases were born before the year 1965. Past evidence showed that in Saudi Arabia, like other neighboring countries, most of the health and educational indicators did not reflect a satisfactory level of protection from exposure to blood borne contaminants including viral hepatitis [29, 30]. Such protective measures include among others, the unsafe and unprotected blood transfusion or the use of such phlebotomy procedure as one of the most common invasive procedures in health care for either the collection of blood or the injection of patients with medications. It was common to see a phlebotomist carry out such procedures known to increase the risk of needle-stick injury and transmission of blood borne infective microorganisms include viruses [9, 31, 32].

Future prediction of HCV genotype 1

In Saudi Arabia as in most countries in the region, blood transfusion is quite recent therapeutic measure [33]. Nowadays, it is mandatory to undertake screening for the two major hepatitis viruses (HCV and HBV) in all donated blood in the country, and this includes testing for HCV (anti-HCV HCV RNA) and HBV (anti-HBc as well as the HBV RNA using molecular techniques) [16, 20]. Based on our assumption on HCV infection being more common disease among the old generations and with predominance of genotype 4, this status is certainly changing in the near future. There will probably be a tremendous decline in HCV infection rate, particularly the rate of genotype 4 but with dominance of genotype 1, thereby conforming with worldwide distribution of this genotype [26, 27]. Some studies have shown a clear decline in the incidence of HCV infection in the Saudi Arabia in comparison with previous data from the year 1990, with more decline among children compared to adults [9, 34]. This was explained by the fact that the perinatal and childhood transmission was not a major mode of transmission as assumed before the last three decades [34]. Blood transfusion is safer today than previously and is no longer a risk for HCV, HBV, or HIV transmission in the region, particularly after the improvements in the quality of blood supply with especial reliable screening tests and consequent reduction in the risk of transfusion-transmitted infectious diseases [26, 35, 36]. However, despite the availability of effective measures to ensure the quality and safety of blood and blood products, recently, the WHO has urged regional member states to ensure transfusion safety by promoting safe blood donation, reduce the risk associated with the clinical use, injection safety and infection control in the health care setting, and reducing the resort for unnecessary injections [37]. Issues concerning the safety of blood during the past 25 years have been associated with changes in blood use and triggered reevaluation of the clinical practices of blood transfusion [36]. Moreover, the role of health education and the high average income probably allowed more and better access to educational resources in preventive care including physician advice; all together played an important role in the reduction in the transmission of infection [38].

Although some early studies explored the dominance of HCV genotypes 4 in Saudi Arabia, the majority of these studies did not show the differences in genotypes according to age, Saudis versus non-Saudis, or other ethnicity related factors [7, 17, 18, 39, 40]. A recent study from KSA, showed increased trend of HCV genotype 1 among those below 50 years old in comparison to genotype 4 in the same age group (46.4% vs. 44.8%) [12]. Interestingly reports from Bahrain and the United Arab Emirates found genotype 1 to be dominant among the studied population [10, 41,42,43]. It is known that different genotypes of hepatitis C virus predominate in different regions of the globe. HCV genotypes 1, 2, and 3 can be found across the globe, while genotype 4 is mainly found in the Middle Eastern or African countries [7, 44, 45]. Confirming this observation, the present study found that 60% of the selected participants had genotype 4 HCV.

The current study has also compared the relationship between HCV genotypes and viral load (viremia level). Viral load refers to the number of virus particles present in the serum or blood. In this study, male patients demonstrated higher rates of viral load than female patients and that viral load was three times more in genotype 1 than genotype 4. Our findings were disagree with those of Al Zayed et al. where viral load levels (IU/ml) were more found with higher reading among patients with genotype 4; however, this could be due to the fact that this sample size was much smaller than our study [12]. Besides, our findings also disagreement from Indian results which showed that the viral load was higher in genotype 1 indicating that viral clearance of the virus was also delayed. This probably exacerbates the occurrence of higher rates of complications and chronicity of liver disease among their population [46, 47].

On the other hand the biochemical profiles showed a significant association of AST with genotype 1 and ALT with genotype 4. Clearly, the interaction between the virus and these enzyme in such population infected with HCV genotype 1 in particular needs more clarification and further definitions in large prospective studies.

Although, the rate of co-infections with HBV or HIV in the present study was very low in concordance with the genotypes, our findings demonstrated that patients infected with HCV genotype 4 did not carry any co-infection. This raises the question whether the genotype of HCV is a determinant factor of co-infection with other types of hepatitis viruses and/or with HIV for example? Further studies are needed on the association of other hepatitis viral infections with the specific genotype of HCV.

Factors related to blood transfusion practices:

In Saudi Arabia, blood supply has shifted dramatically from imported blood, to paid donors and, lately, to the current total dependence on the indigenous predominantly voluntary donators with some contribution from donors mainly family members of patients [9]. However, some studies showed that the rate of blood donation among Saudis was less than satisfactory, probably due to misconceptions, poor knowledge and unfavorable attitudes towards donation [48,49,50,51,52].

As to the possible transmission of some of these transfusion-transmitted infectious diseases some of the patients in the present study, in the mid 1970–1990, must have received blood products mainly in the form of imported blood products which could have been contaminated by some of the viral agents including HCV before the era of the introduction of sensitive screening laboratory tests.

In his recent study on the epidemic dynamics of HCV Al-Qahtani has demonstrated clearly that genotype 4 was transmitted between countries in the region but originated from Egypt. Viral spread between Saudi Arabia and Egypt is predominantly directed towards Saudi Arabia, showing that both HCV genotype 4 epidemics are connected through a source-sink relation, perhaps linked to the large flow of Egyptian migrant workers [53].

Most of the studies including those by the WHO reported HCV prevalence in Saudi Arabia in the range of 0.4 to 1.1% [24, 54,55,56], which means that the rate of the infection categorizes the country among those with the lowest prevalence of HCV in the region, according to WHO classification [57].

This overall reduction in exposure rate may be due to several factors including public awareness of the disease, more and better access to health educational resources such as internet as well as preventive health care. Moreover, the improvement of socio-economic conditions and the level of general education might have also changed the social behavior and cultural habits resulting in reduction in the risks of contamination, in addition to the improvement in donor screening including the use of highly sensitive laboratory assays [38, 39].

Other measures have been undertaken by the government, such as the barring expatriate who are HCV carrier or chronic HBV carriers when applying for jobs in the KSA. No doubt these steps helped in limiting the sources of infection in the country34. Besides, the successful and effective therapy of chronic hepatitis C patients is now available in the KSA and this step helped in removing the residual sources of new infections. All these steps are expected to play a major contributory role in future in the transformation of the dominant genotype in the country40.

Converted rates of HCV genotypes were demonstrated in our study among the young and young adult generation (< 50 years old). This is probably due to the increased risk of being infected with the HCV genotype 1 among the non-Saudi residents in whom this genotype is dominant in their home countries. A study by Bashawri et al., (2004) found a higher rate of HCV genotype 1 among non-Saudi blood donors than Saudi donors36.

Nowadays, it is crucial to have detailed understanding of the relative HCV genotype prevalence and subtypes in the country and also to develop national treatment strategies including direct acting antiviral therapies. The outcome of such strategies will also facilitate undertaking therapeutic programs that will eventually show a clear cut-off point for the required duration of treatment, cure rates, and the need for interferon and other HCV anti-drugs.

According to our knowledge this is the first study of its types in Saudi Arabia on the correlation between the different HCV genotypes and their contribution to the liver and viral biomarkers.

Conclusion

Although HCV Genotype 4 shows an overall high prevalence in the current cohort of the infected Saudi patients, a clear decline in the rate of this genotype was also demonstrated in particular among the younger age group. This is taken to indicate a trend in the transformation in the mapping of HCV genotypes towards the globalize dominance of genotype 1. This situation is not unique for Saudi Arabia but probably so in many other Arabic Gulf countries. The findings of this study could be of great value for those in clinical practice encouraging them to undertake the quantifying of the viral load before designing strategies for therapies in patients suffering from HCV infection. Further broad-based and age-stratified studies should be carried out to determine the future genotype mapping of HCV across the country.

Abbreviations

ALP:

Alkaline phosphates

ALT:

Alanine transaminase

AST:

Aspartate amino transaminase

CPHHI:

College of Public Health and Health Informatics

HBV:

Hepatitis B virus

HCV:

Hepatitis C virus

HIV:

Human Immunodeficiency virus

IRB:

Institutional Review Board

IU/ml:

International Unit per milliliter

KAIMRC:

King Abdullah International Medical Research Center

KSA:

Kingdom of Saudi Arabia

KSAU-HS:

King Saud bin Abdulaziz University for Health Sciences

LIS:

Laboratory Information System

MPL:

Molecular Pathology Laboratory

PCR:

Polymerase chain reaction

QCPR:

QuadraMed Clinical Pathology Record

TB:

Total bilirubin

References

  1. Galdino AS, Santos JC, Souza MQ, Nobrega YK, Xavier MA, Felipe MS, et al. A novel structurally stable Multiepitope protein for detection of HCV. Hepat Res Treat. 2016;6592143(10):28.

    Google Scholar 

  2. Ly KN, Xing J, Klevens RM, Jiles RB, Ward JW, Holmberg SD. The increasing burden of mortality from viral hepatitis in the United States between 1999 and 2007. Ann Intern Med. 2012;156:271–8. https://www.ncbi.nlm.nih.gov/pubmed/22351712.

  3. Supram HS, Gokhale S, Sathian B, Bhatta DR. Hepatitis B virus (HBV) and hepatitis C virus (HCV) co-infection among HIV infected individuals at tertiary Care Hospital in Western Nepal. Nepal J Epidemiol. 2015;5(2):488–93.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Petruzziello A, Marigliano S, Loquercio G, Cozzolino A, Cacciapuoti C. Global epidemiology of hepatitis C virus infection: an up-date of the distribution and circulation of hepatitis C virus genotypes. World J Gastroenterol. 2016;22(34):7824–40. https://www.ncbi.nlm.nih.gov/pubmed/27678366.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Perz JF, Armstrong GL, Farrington LA, Hutin YJ, Bell BP. The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide. J Hepatol. 2006;45(4):529–38. https://www.ncbi.nlm.nih.gov/pubmed/16879891.

    Article  PubMed  Google Scholar 

  6. Chidi AP, Rogal S, Bryce CL, Fine MJ, Good CB, Myaskovsky L, et al. Cost-effectiveness of new antiviral regimens for treatment-naïve US veterans with hepatitis C. Hepatology. 2016;63(2):428–36.

    Article  PubMed  Google Scholar 

  7. Karkar A. Hepatitis C in dialysis units: the Saudi experience. Hemodial Int. 2007;11(3):354–67.

    Article  PubMed  Google Scholar 

  8. Abdo AA, Sanai FM, Al-Faleh FZ. Epidemiology of viral hepatitis in Saudi Arabia: are we off the hook? Saudi J Gastroenterol. 2012;18(6):349–57. http://www.ncbi.nlm.nih.gov/pubmed/23150019.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Gader AGMA, Osman AMA, Al Gahtani FH, Farghali MN, Ramadan AH, Al-Momen AKM. Attitude to blood donation in Saudi Arabia. Asian J Transfus Sci. 2011;5(2):121.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Abdulla MA, Murad EA, Aljenaidi HA, Aljowder DR, Aljeeran OI, Farid E, et al. Interrelationship of hepatitis C virus genotypes with patient characteristics in Bahrain. Hepatic med. 2017;9:7.

    Article  Google Scholar 

  11. Sadeghi F, Salehi-Vaziri M, Almasi-Hashiani A, Gholami-Fesharaki M, Pakzad R, Alavian SM. Prevalence of hepatitis C virus genotypes among patients in countries of the eastern Mediterranean regional office of WHO (EMRO): a systematic review and meta-analysis. Hepat Mon. 2016;16(4):e35558.

    PubMed  PubMed Central  Google Scholar 

  12. Al Zayed RM, Hamdy NM, Al-Ajlan HH, Aref NM. Prevalence of HCV genotypes and viral load in Saudi Arabia. Int J Intern Med. 2015;4(2):26–41.

    Google Scholar 

  13. Al Balwi MA. Prevalence of mixed hepatitis C virus (HCV) genotypes among recently diagnosed dialysis patients with HCV infection. sjkdt. 2011;22(4):712. https://www.ncbi.nlm.nih.gov/pubmed/21743215.

    Google Scholar 

  14. Bosmans J, Nouwen E, Behets G, Gorteman K, Huraib S, Shaheen F, et al. Prevalence and clinical expression of HCV-genotypes in haemodialysis-patients of two geographically remote countries: Belgium and Saudi-Arabia. Clin Nephrol. 1997;47(4):256–62.

    CAS  PubMed  Google Scholar 

  15. Hajeer A, Al Knawy B, Alhaj-Hussein B, Al-Rubiaan S. Hepatitis B virus: a study of genotypes in an infected Saudi cohort. Br J Biomed Sci. 2007;64(2):93.

    CAS  PubMed  Google Scholar 

  16. Alzahrani AJ. Simultaneous detection of hepatitis C virus core antigen and antibodies in Saudi drug users using a novel assay. J Med Virol. 2008;80(4):603–6. https://www.ncbi.nlm.nih.gov/pubmed/21743215.

    Article  PubMed  Google Scholar 

  17. Abdel-Moneim AS, Bamaga MS, Shehab GM, Abu-Elsaad SAA-A, Farahat F. HCV infection among Saudi population: high prevalence of genotype 4 and increased viral clearance rate. PLoS One. 2012;7(1):e29781. https://doi.org/10.1371/journal.pone.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Boriskin YS, Bakir TM. Al-Aska AI, booth JC. Is hepatitis C virus genotype 4 predominant in Saudi Arabia? New Microbiol. 1999;22(3):173–80. https://www.ncbi.nlm.nih.gov/pubmed/10423734.

    CAS  PubMed  Google Scholar 

  19. Zhao R, Peng J, Tang L, Huang H, Liu M, Kong W, et al. Epidemiological distribution and genotype characterization of hepatitis C virus and HIV co-infection in Wuhan, China, where the prevalence of HIV is low. J Med Virol. 2013;85(10):1712–23. http://www.ncbi.nlm.nih.gov/pubmed/23868809.

    Article  CAS  PubMed  Google Scholar 

  20. Khan A, Al Balwi M, AlAyyar L, AlAbdulkareem I, Albekairy A, AlJumah A. Tracing the epidemic history of hepatitis C virus genotypes in Saudi Arabia. Infect Genet Evol. 2017;52:82–8.

    Article  PubMed  Google Scholar 

  21. Al-Faleh F, Huraib S, Sbeih F, Al-Karawi M, Al-Rashed R, Al-Mofleh I, et al. Hepatitis C virus genotypes in patients with chronic liver disease and haemodialysis patients from Saudi Arabia. J Viral Hepat. 1995;2(6):293–6. www.ncbi.nlm.nih.gov/m/pubmed/8732175.

    Article  CAS  PubMed  Google Scholar 

  22. Shobokshi OA, Serebour FE, Skakni LI. Hepatitis C genotypes/subtypes among chronic hepatitis patients in Saudi Arabia. Saudi Med J. 2003;24(7):87–91.

    Google Scholar 

  23. Al-Traif I, Handoo FA, Al-Jumah A, Al-Nasser M. Chronic hepatitis C. Genotypes and response to anti-viral therapy among Saudi patients. Saudi Med J. 2004;25(12):1935–8. https://www.ncbi.nlm.nih.gov/pubmed/15711670.

    PubMed  Google Scholar 

  24. Memish ZA, Al Knawy B, El-Saed A. Incidence trends of viral hepatitis a, B, and C seropositivity over eight years of surveillance in Saudi Arabia. Int J Infect Dis. 2010;14(2):e115–20. https://www.ncbi.nlm.nih.gov/pubmed/19540786.

    Article  PubMed  Google Scholar 

  25. Louie KS, St Laurent S, Forssen UM, Mundy LM, Pimenta JM. The high comorbidity burden of the hepatitis C virus infected population in the United States. BMC Infect Dis. 2012;12(1):1.

    Article  Google Scholar 

  26. Messina JP, Humphreys I, Flaxman A, Brown A, Cooke GS, Pybus OG, et al. Global distribution and prevalence of hepatitis C virus genotypes. Hepatology. 2015;61(1):77–87.

    Article  PubMed  Google Scholar 

  27. 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;61:45–57.

    Article  Google Scholar 

  28. Qasim L, Abed E, Memish Z, AlBasheer A. Pattern of viral hepatitis infection in a selected population from Saudi Arabia. Mil Med. 2003;168(7):565–8.

    PubMed  Google Scholar 

  29. Sebai ZA, Milaat WA, Al-Zulaibani AA. Health care services in Saudi Arabia: past, present and future. J Family Community Med. 2001;8(3):19–23. https://www.ncbi.nlm.nih.gov/pubmed/23008647.

    CAS  PubMed  PubMed Central  Google Scholar 

  30. Almalki M, Fitzgerald G, Clark M. Health care system in Saudi Arabia: an overview. East Mediterr Health J. 2011;17(10):784–93. https://www.ncbi.nlm.nih.gov/pubmed/22256414.

  31. World Health Organization. WHO guidelines on drawing blood: best practices in phlebotomy. 2010. Available at: http://whqlibdoc.who.int/publications/2010/9789241599221_eng.pdf. Accessed 18 Nov 2016.

  32. World Health Organization (WHO). Infection prevention and control during health care for probable and confirmed cases of novel coronavirus (nCov) infection. http://www.who.int/csr/disease/coronavirus_infections/IPCnCoVguidance_06May13.pdf. Accessed 22 Mar 2016.

  33. Daw MA, Dau AA. Hepatitis C virus in Arab world: a state of concern. Sci World J. 2012;2012:719494. https://www.hindawi.com/journals/tswj/2012/719494/.

    Google Scholar 

  34. Alqahtani JM, Abu-Eshy SA, Mahfouz AA, El-Mekki AA, Asaad AM. Seroprevalence of hepatitis B and C virus infections among health students and health care workers in the Najran region, southwestern Saudi Arabia: the need for national guidelines for health students. BMC Public Health. 2014;14:577. https://bmcpublichealth.biomedcentral.com/articles/10.1186/1471-2458-14-577.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Cheraghali AM. Blood safety concerns in the eastern Mediterranean region. Hepat Mon. 2011;11(6):422–6.

    PubMed  PubMed Central  Google Scholar 

  36. Bashawri LA. Pattern of blood procurement, ordering and utilization in a University Hospital in Eastern Saudi Arabia. Saudi Med J. 2002;23(5):555–61. https://www.ncbi.nlm.nih.gov/pubmed/12070581.

    PubMed  Google Scholar 

  37. WHO. Strategic framework for blood safety and availability 2016–2025. Cairo: World Health Organization, Regional Office for the Eastern Mediterranean; 2017. http://applications.emro.who.int/dsaf/EMROPub_2017_EN_19608.pdf?ua=1.

    Google Scholar 

  38. Al-Thaqafy MS, Balkhy HH, Memish Z, Makhdom YM, Ibrahim A, Al-Amri A. Improvement of the low knowledge, attitude and practice of hepatitis B virus infection among Saudi national guard personnel after educational intervention. BMC Res Notes. 2012;5:597. https://bmcresnotes.biomedcentral.com/articles/10.1186/1756-0500-5-597.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Al-Humayed SM. Hepatitis B and C viral infections in Tihamet Aseer,South-western Saudi Arabia: are there gender differences? Saudi J Med Med Sci. 2017;5:110–5. http://www.sjmms.net/temp/SaudiJMedMedSci52110-4814988_132229.pdf.

    Google Scholar 

  40. Shobokshi OA, Serebour FE, Al-Drees AZ, Mitwalli AH, Qahtani A, Skakni LI. Hepatitis C virus seroprevalence rate among Saudis. Saudi Med J. 2003;24(7):81–6. https://www.smj.org.sa/index.php/smj/article/viewFile/4295/2069

    Google Scholar 

  41. Abdulla MA, Al Qamish JR. Hepatitis C virus infection: a single center experience. Bahrain Med Bull. 2008;30(1):3–8.

    Google Scholar 

  42. Mohamoud YA, Riome S, Abu-Raddad LJ. Epidemiology of hepatitis C virus in the Arabian gulf countries: systematic review and meta-analysis of prevalence. Int J Infect Dis. 2016;46:116–25. http://www.ijidonline.com/article/S1201-9712(16)30999-7/pdf.

    Article  PubMed  Google Scholar 

  43. Abro AH, Al-Dabal L, Younis NJ. Distribution of hepatitis C virus genotypes in Dubai, United Arab Emirates. J Pak Med Assoc. 2010;60(12):987–90. http://jpma.org.pk/PdfDownload/2448.pdf.

    PubMed  Google Scholar 

  44. Kanwal F, Hoang T, Kramer JR, Asch SM, Goetz MB, Zeringue A, et al. Increasing prevalence of HCC and cirrhosis in patients with chronic hepatitis C virus infection. Gastroenterol. 2011;140(4):1182–8. e1181

    Article  Google Scholar 

  45. Antaki N, Craxi A, Kamal S, Moucari R, Van der Merwe S, Sea H. The neglected hepatitis C virus genotypes 4, 5 and 6: an international consensus report. Liver Int. 2010;30:342–55. http://onlinelibrary.wiley.com/doi/10.1111/j.1478-3231.2009.02188.x/pdf.

    Article  CAS  PubMed  Google Scholar 

  46. Chakravarti A, Dogra G, Verma V, Srivastava AP. Distribution pattern of HCV genotypes & its association with viral load. Indian J Med Res. 2011;133:326–31. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103160/.

    PubMed  PubMed Central  Google Scholar 

  47. Malik YP, Kumar N, Rawat V, Sharma K, Kumar A, Singhai M, et al. Detection and distribution pattern of prevalent genotypes of hepatitis-C virus among chronic hepatitis patients from Kumaon region of Uttarakhand, India. Indian J Med Microbiol. 2015;33(Suppl):161–3. http://www.ncbi.nlm.nih.gov/pubmed/25657142.

    PubMed  Google Scholar 

  48. Alfouzan N. Knowledge, attitudes, and motivations towards blood donation among king Abdulaziz Medical City population. Int J Family Med. 2014;2014:539670. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238271/.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Abolfotouh A, Al-Assiri MH, Al-Omani M, Al Johar A, Al Hakbani AS. AS. A. Public awareness of blood donation in Central Saudi Arabia. Int J Gen Med. 2014;7:401–10. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140232/pdf/ijgm-7-401.pdf.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Tayi A, Alhatlan M, AlBujays IA, Saleh A. Blood donation among Al-Ahsa population in Saudi Arabia: attitudes, practice and obstacles. Blood. 2016;101:1.73–72.99.

    Google Scholar 

  51. Al-Drees AM. Attitude, belief and knowledge about blood donation and transfusion in Saudi population. Pak J Med Sci. 2008;24:74–9. http://pjms.com.pk/issues/janmar08/pdf/transfusion.pdf.

    Google Scholar 

  52. Al-Faris AK, Bahabri AS, Al-Aqeel AA, Al-Momi MS, Al-Dojain MK, Al-Zahem TA, et al. Attitude to blood donation among male students at King Saud University. J Appl Hematol. 2013;4:70–7.

    Google Scholar 

  53. Al-Qahtani AA, Baele G, Khalaf N, Suchard MA, Al-Anazi MR, Abdo AA, et al. The epidemic dynamics of hepatitis C virus subtypes 4a and 4d in Saudi Arabia. Sci Rep. 2017;7:44947. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359580/pdf/srep44947.pdf.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Bashawri L, Fawaz N, Ahmad M, Qadi A, Almawi W. Prevalence of seromarkers of HBV and HCV among blood donors in eastern Saudi Arabia, 1998–2001. Clin Lab Haematol. 2004;26(3):225–8. https://www.ncbi.nlm.nih.gov/pubmed/15163322.

    Article  CAS  PubMed  Google Scholar 

  55. El-Hazmi MM. Prevalence of HBV, HCV, HIV-1, 2 and HTLV-I/II infections among blood donors in a teaching hospital in the central region of Saudi Arabia. Saudi Med.J. 2004;25:26–33. https://www.ncbi.nlm.nih.gov/pubmed/14758374.

    PubMed  Google Scholar 

  56. Mehdi SR, Pophali A, Rahim KA-A. Prevalence of hepatitis B and C and blood donors. Saudi MedJ. 2000;21(10):942–4. https://www.ncbi.nlm.nih.gov/pubmed/11369958.

    CAS  Google Scholar 

  57. World Health Organization: The growing threats of hepatitis B and C in the Eastern Mediterranean region: a call for action. Technical Paper EM/RC56/3. 2009. Available from: http://applications.emro.who.int/docs/EM_RC56_3_en.pdf. Accessed 15 Nov 2017.

Download references

Acknowledgements

The authors acknowledge and grateful to Ms. Zoe P. Camarig for her secretarial support in reviewing and editing the manuscript. Also we are highly appreciate King Abdullah International Medical Research Center (KAIMRC) for helping in publishing this manuscript.

Funding

Not applicable.

Availability of data and materials

Materials described in the manuscript are freely available to any scientist wishing to use them.

Author information

Authors and Affiliations

Authors

Contributions

AB developed the idea and the project. FA and MA for data collection. AB and HJ data analysis. FA and AB develop the result, discussion. AB draft the manuscript. All authors AB, FA, AG, MA, and HJ edited, read and approved the final version of the manuscript.

Corresponding author

Correspondence to Amen Bawazir.

Ethics declarations

Ethics approval and consent to participate

No informed consent was needed since the analyzed laboratory data was secondary (without names or identity). Nonetheless, this study was reviewed and approved by the internal Institutional Review Board (IRB) in the College of Public Health and Health Informatics (CPHHI), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) and King Abdullah International Medical Research Center (KAIMRC) under # SP 14/053.

Consent for publication

Not applicable.

Competing interests

The author declares they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bawazir, A., AlGusheri, F., Jradi, H. et al. Hepatitis C virus genotypes in Saudi Arabia: a future prediction and laboratory profile. Virol J 14, 208 (2017). https://doi.org/10.1186/s12985-017-0873-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12985-017-0873-7

Keywords