Prevalence and risk factors of hepatitis B and C virus infections among the general population and blood donors in Morocco

  • Warda Baha1, 2,

    Affiliated with

    • Abderrahim Foullous1,

      Affiliated with

      • Noureddine Dersi1,

        Affiliated with

        • Thierry Paluku They-they3, 4,

          Affiliated with

          • Khadija El alaoui3,

            Affiliated with

            • Nadia Nourichafi3,

              Affiliated with

              • Bouchra Oukkache4,

                Affiliated with

                • Fatiha Lazar1,

                  Affiliated with

                  • Soumaya Benjelloun1,

                    Affiliated with

                    • My Mustapha Ennaji2,

                      Affiliated with

                      • Abdelouhad Elmalki1,

                        Affiliated with

                        • Hassan Mifdal3 and

                          Affiliated with

                          • Abdelouaheb Bennani1Email author

                            Affiliated with

                            BMC Public Health201313:50

                            DOI: 10.1186/1471-2458-13-50

                            Received: 22 June 2012

                            Accepted: 15 January 2013

                            Published: 18 January 2013

                            Abstract

                            Background

                            Viral hepatitis is a serious public health problem affecting billions of people globally. Limited information is available on this issue in Morocco. This cross-sectional study was undertaken with the aim of determining the seroprevalence and risk factors of hepatitis B virus (HBV) and hepatitis C virus (HCV) among the general population and among blood donors.

                            Methods

                            Blood samples from volunteers, have been screened with ELISA tests for detecting the hepatitis-B surface antigen (HBsAg) and anti-HCV. Within the seroreactive patients for HCV in the general population, RT-PCR was performed by the Cobas Ampliprep/Cobas Amplicor.

                            Results

                            HCV and HBV-seropositivity was documented in 1.58% and 1.81% out of 41269 and 23578 participants respectively from the general population. Two patients were found to be co-infected. HCV-RNA was detected by PCR in 70.9% of the 195 anti-HCV positive subjects. The anti-HCV prevalence was not different among males and females (P = 0.3). It increased with age; the highest prevalence was observed among subjects with >50 years old (3.12%). Various risk factors for acquiring HCV infection were identified; age, dental treatment, use of glass syringes and surgical history. In addition to these factors, gender and sexual risk behaviors were found to be associated with higher prevalence of hepatitis B. The HBV positivity was significantly higher among males than females participants in all age groups (P < 0.01). The peak was noticed among males aged 30–49 years (2.4%). None of the 152 persons younger than 20 years had HBsAg or anti-HCV. The prevalence of anti-HCV and HBsAg among 169605 blood donors was 0.62% and 0.96% respectively.

                            Conclusions

                            Our study provided much important information concerning hepatitis B and C prevalence and risk factors; it confirmed the intermediate endemicity for HCV infection and pointed to a decreasing trend of HBV incidence, which might reclassify Morocco in low HBV endemicity area. This could be attributed primarily to the universal HBV vaccination among infants and healthcare workers over the past 13 years. HCV and HBV infections in the present survey were mainly associated with nosocomial exposures. Prevention and control of HBV infection are needed to reduce HBV transmission between adults.

                            Keywords

                            Hepatitis B Hepatitis C Prevalence General population Risk factors Blood donors Morocco

                            Background

                            Hepatitis B virus (HBV) and hepatitis C virus (HCV) are among the principal causes of severe liver disease, including hepatocellular carcinoma (HCC) and cirrhosis-related end-stage liver disease. The World Health Organization (WHO) has estimated that there are 360 million chronically HBV infected people and 5.7 million HBV-related cases worldwide [1]. HBV is highly infectious and transmitted mainly via blood, body-fluid contact, and vertical transmission [2]. The hepatitis B surface antigen (HBsAg) in serum is the first seromarker to indicate active HBV infection, either acute or chronic [3]. A hepatitis B vaccine, available since 1982, has a high efficacy in the prevention of HBV transmission [2] and has brought about remarkable changes in the global epidemiology of HBV infection. HCV infection is also common worldwide. It is transmitted in a manner similar to HBV and it is estimated that about 3% of the world’s population carry HCV, with 3 to 4 million new infections per year [4]. Hepatitis C is generally asymptomatic, with a strong tendency (up to 80%) for progression to persistent infection [5]. Chronic HCV infection progresses at a variable rate to cirrhosis in 15 to 20% of patients, who then have a 1 to 4% annual risk of developing hepatocellular carcinoma in 20–30 years [6].

                            Morocco has been placed by the WHO into the intermediate zone of prevalence for both hepatitis B and C; however the exact number of persons infected is unknown for the reason that no large-scale epidemic data exist to assess the true HCV and HBV infection burden in Morocco. Although a few studies have been carried out, they were affected by a selection bias because most studies are generally based on subjects from risk groups or blood donors with lacking information on children and senior citizens not generally included in as specialized groups [79].

                            The scarcity of data and the degree to which they are out of date were the main reasons behind a nationwide cross-sectional survey aimed to determine the prevalence and risk factors of HCV and HBV infections in the general population and among blood donors to unravel the true status of viral hepatitis in apparently healthy Moroccan persons and thus provide valuable information about surveillance and estimation.

                            Methods

                            Study design, setting and population

                            General population

                            This was a nationwide cross-sectional survey enrolling in the large screening program for hepatitis B and C conducted by the Pasteur Institute of Morocco and carried out in eleven major Moroccan regions between December 2005 and June 2011. The target subjects in this study were the apparently healthy Moroccan individuals which were selected to be as representative of the demographic characteristics as possible in regarding areas of Morocco. To construct the national probability sample, a stratified, random cluster sampling method was used to select the study population. In the first stage, names of private and public organizations (companies, agencies, banks, factories, schools…) from different prefectures and provinces of regions were obtained using directories. Lists were compiled using excel tool to select 288 organisms. To invite the selected structures to participate in the survey, a letter was sent with standardized information regarding the study. Each organism has agreed to participate provided a list of the active or retired personnel (also students in case of schools). The study population was selected by a systematic 1:3 sampling procedure; every third person from each list was selected and approached for participation. The study was also open for all persons who wish to participate.

                            The investigative team performing the fieldwork consisted of physicians who performed clinical examination, paramedics who collected blood samples, and trained social workers who explain the objectives of the study and interview each participant. No willful participation was allowed and if any eligible candidate declined to participate, his or her name was dropped from the list of participants. An informed consent was obtained from the participating subjects and, in the case of the minors, the parents or tutors. A standard and individual questionnaire was used to gather data related to demographic and socio-economic characteristics, age, gender, present and past health status, history of jaundice, and possible risk factors for transmitting viral hepatitis.

                            In the end, 280 structures (97.3%) and 41 269 out of 41 311 participants (99.9%) agreed to participate in the survey. The first 17 691 persons recruited were tested only for anti-HCV Ab and the subsequent 23 578 persons were tested for both anti-HCV and HBsAg. All subjects were grouped by sex and age range. The collected blood was transferred to the Molecular Biology Laboratory at Pasteur Institute of Morocco under sterile conditions in ice bags, separated and stored at −70°C until laboratory testing was performed.

                            The HBsAg and the IgG antibodies to HCV markers were serologically assessed using a third generation enzyme immunoassay (Murex HBsAg Version 3, Abbott-Murex, South Africa) and (Murex, anti-HCV version 4.0 Abbott Kyalami, South Africa) respectively. Positive samples were retested for confirmation using an automated microparticle enzyme immunoassay (Abbott, AxSYM. System, Wiesbaden, Germany).

                            Anti-HCV–positive subjects were recalled for further evaluation at a subsequent date. A detailed clinical examination was performed and blood samples were further assessed for HCV RNA by polymerase chain reaction using the Cobas Ampliprep/Cobas Amplicor HCV Test (Roche diagnostics, Mannheim, Germany), (limit of detection 50 IU/ml).

                            Blood donors

                            The participants in this cross-sectional study were all volunteer blood donors who donated blood at the Casablanca Regional Blood Transfusion Center between January 1st, 2008 and December 31, 2010.

                            The donors were interviewed by physicians before donation; each donor was requested to fill a blood donor’s form and was obliged to satisfy the center’s criteria: age over 18 and less than 65, body weight over 50 kg, normal body temperature, absence of clinical signs of an acute infective response, no history of infectious and chronic diseases and information about any high-risk behavior. Therefore all participants selected in this study are presumed without a history of known or obvious risk factor. Care was also taken to make sure that no donor was used more than once in this study. Unsuitable donors were excluded.

                            All blood samples were routinely screened for transfusion-transmitted diseases (HBV, HCV, HIV and Syphilis) according to established screening procedures and tests; hence specimens were tested for HBsAg and anti-HCV antibodies by Murex HBsAg Version 3 and Murex Ag/Ab HCV Combination Assay (Abbott-Murex, South Africa) respectively. Reactive samples were retested in duplicate. Repeatedly reactive samples were confirmed by means of recombinant immunoblot assay for HCV (RIBA, Innogenetics). Samples were considered to be positive if were reactive for both tests.

                            All procedures were followed in accordance with the current revision of the declaration of Helsinki, approved by the ethical committee of Pasteur Institute of Morocco.

                            Statistical analysis

                            Statistical analyses were performed by using SPSS 16.0 software. The overall prevalence of HCV and HBV markers was expressed as the percentage of seropositive samples. The prevalence odds ratios (OR) and Confidence intervals (CI) of 95% for OR estimates were also estimated. A level of p < 0.05 was used to indicate statistical significance.

                            Results

                            General population

                            In all, 41 269 (sex-ratio (M/F) = 2.30) serum samples were tested for anti-HCV Ab analysis and 23 578 (sex-ratio (M/F) = 1.84) subjects were enrolled for HBsAg detection. The overall mean age was 45 (± 10.9) years, ranging from 5 to 84 years.

                            The seroprevalence of anti-HCV Ab was found to be 1.58%, corresponding to 651 seropositive patients out of 41 269 participants, of those individuals, viral RNA was detected in 70.9%. The prevalence of anti-HCV in the <20, [20–29], [30–39], [40–49] and >50 age groups was 0%, 0.77%, 0.92%, 1.17% and 3.12%, respectively. For those subjects, the anti-HCV prevalence increased with age (Figure 1A).
                            http://static-content.springer.com/image/art%3A10.1186%2F1471-2458-13-50/MediaObjects/12889_2012_5248_Fig1_HTML.jpg
                            Figure 1

                            Serological features of anti-HCV prevalence in Morocco. Bars represent the number of subjects in each group indicated by left vertical axis, and the points represent the prevalence in each group indicated by right vertical axis. The horizontal axis represents the age ranges. A, Overall characterization of anti-HCV by age group. B, Overall characterization of anti-HCV by gender, M, male, F, female.

                            The overall prevalence of anti-HCV in 12 497 female subjects was 1.48% (185 positive), which was lower than that in the 28 772 male subjects, 1.62% (466 positive). For those subjects younger than 30 years, the prevalence of anti-HCV in females was lower than that in males, then it increased and became higher than that in males in >30 age groups (Figure 1B).

                            The overall prevalence of HBsAg was 1.81% (426 positive) in 23578 subjects. HBsAg prevalence in <20, [20–29], [30–39], [40–49] and >50 age groups was 0%, 1.41%, 2.12%, 1.95% and 1.71%, respectively, as well as it showed an increase with age from 1.41% in [20–29] group to 2.12% and 1.95% in [30–39] and [40–49] group respectively, then decrease in the older group >50 years old to 1.71% (Figure 2A).
                            http://static-content.springer.com/image/art%3A10.1186%2F1471-2458-13-50/MediaObjects/12889_2012_5248_Fig2_HTML.jpg
                            Figure 2

                            Serological features of HBsAg prevalence in Morocco. Bars represent the number of subjects in each group indicated by left vertical axis, and the points represent the prevalence in each group indicated by right vertical axis. The horizontal axis represents the age ranges. A, Overall characterization of HBsAg by age group. B, Overall characterization of HBsAg by gender, M, male, F, female.

                            When the overall prevalence of HBsAg marker was analyzed according to gender, the prevalence was 2.29% and 0.93% in male and female subjects respectively. The difference was found to be statistically significant (P < 0.01), and in all groups it showed higher prevalence in males than that in females (Figure 2B). The males in age groups [30–39] and [40–49] years represent the highest seroprevalence of HBsAg found in this study (2.47% and 2.45% respectively).

                            Regarding the seropositivity of HBV and HCV dual infection, the presence of both HBsAg and anti-HCV antibodies was noted in 2 cases Out of 23 578 tested subjects. These two patients were male subjects who belonged to age groups 20–29 years and ≥50 years respectively.

                            Table  1 lists the frequency of potential risk factors reported by subjects with positive and negative anti-HCV results and the crude OR estimated by univariate analysis. Factors significantly associated with HCV infection were increasing age, dental treatment, use of glass syringes and surgical history. Conversely, no association was observed between HCV seropositivity and gender, receiving blood transfusion, tattooing, body piercing, having multiple sexual partners, acupuncture and endoscopy. On the subject of HBV infection, HBsAg positivity was significantly associated with age, male gender (OR 2.5; p < 0.01), Dental procedure history (OR 3.0; p < 0.01), Use of glass syringes (OR 2.3; p < 0.01), history of jaundice (OR 1.4; p = 0.03) and history of sexual risk behaviors (OR 2.9; p < 0.01).
                            Table 1

                            Distribution of Hepatitis C virus serological marker and principal risk factors in the general population December 2005-June 2011

                            Risk factor

                            HCV-Positive Subjects

                            HCV-Negative Subjects

                            OR

                            (CI 95%)

                            P

                             

                            N

                            %

                            N

                            %

                              

                            Age

                                  

                             <40

                            144

                            0.9

                            16 686

                            99.1

                            2.5 (2.0-2.9)

                            <0.01

                             >40

                            507

                            2.1

                            23 932

                            97.9

                            Sex

                                  

                             Female

                            185

                            1.5

                            12 312

                            98.5

                            0.9 (0.8-1.0)

                            0.3

                             Male

                            466

                            1.6

                            28 306

                            98.4

                            Dental therapy

                                  

                             No

                            244

                            0.8

                            28 351

                            99.2

                            3.8 (3.3- 4.5)

                            <0.01

                             Yes

                            407

                            3.2

                            12 267

                            96.8

                            Use of glass syringes

                                  

                             No

                            329

                            1.2

                            27 905

                            98.8

                            2.1 (1.8- 2.5)

                            <0.01

                             Yes

                            322

                            2.5

                            12 713

                            97.5

                            Surgical history

                                  

                             No

                            403

                            1.4

                            28 027

                            98.6

                            1.37 (1.2-1.6)

                            0.01

                             Yes

                            248

                            1.9

                            12 591

                            98.1

                            Blood transfusion

                                  

                             No

                            546

                            1.6

                            34 566

                            98.4

                            1.1 (0.9-1.4)

                            0.4

                             Yes

                            105

                            1.7

                            6052

                            98.3

                            Piercing/tattoo

                                  

                             No

                            599

                            1.6

                            37 694

                            98.4

                            1.1 (0.8-1.5)

                            0.5

                             Yes

                            52

                            1.7

                            2924

                            98.3

                            Multiple Sexual partners

                                  

                             No

                            634

                            1.6

                            39 806

                            98.4

                            1.3 (0.8-2.1)

                            0.3

                             Yes

                            17

                            2

                            812

                            98

                            Acupuncture

                                  

                             No

                            649

                            1.6

                            40 578

                            98.4

                            3.1 (0.7-12.9)

                            0.3

                             Yes

                            2

                            4.8

                            40

                            95.2

                            Endoscopy

                                  

                             No

                            649

                            1.6

                            40 253

                            98.4

                            0.3 (0.1-1.4)

                            0.2

                             Yes

                            2

                            0.5

                            365

                            99.5

                              

                            OR: Odds ratios, CI: confidence interval.

                            Blood donors

                            A total of 169 605 voluntary blood donors were selected in the Transfusion Blood Center of Casablanca between January 2008 and December 2010 for the study, of whom 79.7% were males. The overall mean age was 35.7 (± 12.5) years, ranging from 18 to 65 years. The seroprevalence was estimated over the three-year study period. Among all analyzed subjects, 1057 were anti-HCV positive, representing an overall prevalence of 0.62% (Table  2). The seroprevalence was 0.57% in 2008 but subsequently increased to 0.64% in 2009 and 2010. Similarly, the prevalence of HBV was slightly increased from 1.1% in 2008 to 1.15% in 2009 and decreased to 0.63% in 2010. The overall seroprevalence rate of HBV was 0.96% corresponding to 1603 HBsAg-positive individuals.
                            Table 2

                            The frequency of seropositivity of HBV and HCV among blood donors at Blood Transfusion Center of Casablanca 2008-2010

                            Year

                            Total screened

                            HCV positive

                            HBV positive

                             

                            N

                            N (%)

                            N (%)

                            2008

                            52 279

                            300 (0.57)

                            575 (1.1)

                            2009

                            55 496

                            357 (0.64)

                            638 (1.15)

                            2010

                            61 830

                            400 (0.64)

                            390 (0.63)

                            Total

                            169 605

                            1057 (0.62)

                            1603 (0.95)

                            N = Number.

                            Discussion

                            We report here a cross-sectional study to assess the epidemiology of HCV and HBV prevalence among the general population residing or working in the major Moroccan regions and among blood donors from the Blood Transfusion Center of Casablanca, the largest commercial and densely populated city of Morocco. To the best of our knowledge this is the largest community-based epidemiologic study of HCV and HBV infections from Morocco. The sampling procedure adopted and the high participation rate (97.3%) support the absence of selection and non-response bias, ensuring thus an accurate assessment of the prevalence in our study. Most of the previous researchers in this field were limited due to the selective nature of the survey populations. The descriptive epidemiologic data presented in this study can provide new insight into the contribution of HCV and HBV in the etiology of liver disease in Morocco.

                            The overall prevalence of HCV infection in the general population in our study is found to be 1.58% and was lower than the prevalence reports from close countries; Algeria (2.5%), Libya (3%) and Egypt (15%-20%) [1012]. Our estimate was also too much lower compared to what has been reported in the prior decade by Cacoub et al.[13] in which the estimated HCV infection rate was 7.7%. This result is surely related to the nature of the participants enrolled in the study who were mostly hospitalized patients and those who come for consultation suffering from chronic hepatopathy or with nephrological manifestations. Most HCV-seropositive subjects in the present survey had detectable viremia (70.9%), which is consistent with findings in studies from France (80.6%) and Italy (75.9%) [14, 15].

                            No statistically significant difference in HCV distribution according to gender was found in our study, which is similar to other reports on community-acquired hepatitis C from United states and Belgium [16, 17], However, higher prevalence was observed in advanced age groups; indeed, no anti-HCV seropositive case was found in 152 subjects in age groups younger than 20 years, nevertheless the seropositivity increased progressively from adults (0.77%) to older persons (3.12%). This can be supported by two major reasons. First, before 1994, anti-HCV screening among blood donors was not conducted throughout Morocco and the association of blood transfusion with HCV seropositivity should not be surprising given that the blood product had not been previously screened for HCV. Second, the higher prevalence of HCV in older people could be attributed to a longer exposure to risk factors for HCV transmission; for instance iatrogenic transmission resulting from inadequately sterilized equipments, inappropriate reuse of supplies, etc. This risk factor is considered the main risk associated with HCV infection in the majority of participants from the general population included in this study. This same risk is the primary cause for HCV transmission in many outbreaks documented in United States and European Union health care [18, 19].

                            Regarding HBV infection, the overall prevalence of HBsAg was significantly lower (1.81%) than that reported from Algeria (3.6%) and Tunisia (4-7%) [20, 21]. Despite the large number of young in <20 group tested (152 subjects), none was positive for HBsAg, These results indicate that the strong efforts made among youngers have had some success since the HBV infant vaccination was introduced in 1992 and integrated into the national immunization program in 1999, in addition, hepatitis B immunoglobulin and HBV vaccine treatment for newborns of HBV-infected mothers at delivery could also contribute to the significant reduction of vertical or perinatal transmission of HBV.

                            On the other hand, the age-related prevalence of HBsAg showed a progressive decrease after 50 years (1.71%), so among participants who were older than 50 years, the prevalence of anti-HCV was higher (3.12%) than that of HBsAg (1.71%). This can be probably due to deaths caused by HBV-related cirrhosis and hepatocellular carcinoma in this group [22]. Additionally, it has been reported that HBV-associated HCC occurs approximately 10 years earlier than HCV-associated HCC [23, 24]. Conversely, on the whole, the prevalence of HBV in our study population was slightly higher than that of HCV (1.81% vs. 1.58%). Thus, the comparative incidence of the two viruses is consistent with findings in studies conducted in India, China and Bosnia-Herzegovina [3, 5, 25].

                            Analysis by gender reveals that, the seroprevalence of hepatitis B among males is significantly higher than that found in females; this data was comparable to other reports [26], and no plausible explanation has been given for the higher rate in males in the general population but probably due to the higher exposure to occupational HBV risk factors in men, or else females clear the HBV more efficiently as compared to males [27].

                            Our research shows a very low prevalence (two cases among 23 578 personts tested) of hepatitis co-infection comparing with Tunisia (5%) and Egypt (22.5%) [28, 29], these results indicate that the HBV positive patients investigated herein do not have an increased risk of exposure to HCV infection. Although this small sample size of reactive cases does not allow data to be compared with other reports, one Italian study found that rates of dual infection increased with age, and was more common in patients over 50 years of age [30]. In this report, the two cases were male subjects belonging to age groups 20–29 years and ≥50 years respectively. Moreover several authors have reported that HBV can reciprocally inhibit HCV replication [31]; specifically, HBV DNA replication has been shown to correlate with decreased HCV RNA levels in coinfected patients [32]. In another Italian study, coinfected patients had a rate of HCV RNA clearance of 71% compared to 14% with HCV monoinfection [31]. Furthermore, coinfected patients have been demonstrated to have lower levels of both HBV DNA and HCV RNA than corresponding mono-infected controls, inicating that concurrent suppression of both viruses by the other virus can also occur [33].

                            After all, according to research regarding HBV prevalence, Morocco has been estimated as a moderately endemic area; thus, in a WHO collaborative study on viral hepatitis B in which 20 countries have participated, the seroprevalence were reported was 3.3% [34]. Among barbers and their customers, the positive ratio for HBsAg was found to be 2.0% by Zahraoui et al. in 2004 and 28.0% by Belbacha et al. in 2011 [7, 35]. Comparison of these findings with the HBsAg carrier rate estimated in this exhaustive investigation and our preliminary results published by Sbai et al.[36], shows that the epidemiological picture is changing and that the vaccination program has shifted this trend to low endemicity.

                            In this study, we also measured over a period of three years, the frequency of HCV and HBV infections among 169 605 voluntary blood donors assumed to be without known or obvious risk factors. 0.62% and 0.96% of subjects were tested positive for HCV antibodies and HBsAg respectively, these results were significantly lower compared with the prevalence observed among the general population reported here. This could be explained by the fact that the volunteer blood donors are a preselected healthy group based on donor questionnaires and physical examination as blood is drawn only from those applicants who appear at low risk of having blood-borne pathogens [37]. Moreover, with regard to HCV infection, this prevalence is considerably lower in comparison with that reported among blood donors in 1998 at the same institution and in 1992 at the Regional Blood Transfusion Center of Rabat (0.70% and 1.56% respectively) [38]. This observation is probably due to the improvement of the effectiveness of the medical selection through self-exclusion from blood donation and medical examination. When the results of the present study were compared with those reported from similar blood donors of other countries, a comparable prevalence of HCV antibodies has been reported in blood donors from Libya (0.69%) and Germany (0.65%) [39, 40]. Studies from Tunisia (1.4 %), Senegal (0.8%) and United States (1.8%) reported higher HCV infection rate [4143], whereas Algeria (0.18 %), Spain (0.3%), England (0.1%), Bosnia and Herzegovina (0.27%) showed lower frequency of the HCV antibodies seropositivity in comparison to the present study [20, 4446].

                            Measurement of HBV seropositivity, has revealed that 0.96% of the Moroccan blood donors had HBV infection. This seroprevalence is lower than that reported in Algeria (3.6%), Libya (1.28%), Turkey (1.8%) and Iran (1.07%) [20, 37, 39, 46]. Nevertheless, it is higher than the reactivity rate reported in Rabat, Morocco (0.8%), a US community (0.15%), and Bosnia-Herzegovina (0.78%) [8, 25, 47].

                            Conclusion

                            Our study throws light for the first time, on the current epidemiological status of viral hepatitis B and C infections in Morocco among the general population and blood donors. This data shows that the prevalence of HBV and HCV in blood donors was significantly lower than that observed in the general population, which emphasizes that the blood transfusion was not a contributing risk factor for transmission of neither HBV nor HCV infection. The main transmission route in Morocco is still attributed to the nosocomial exposure to contaminated instruments.

                            The present survey reports that the HCV infection is at an intermediate level of endemicity. It also underlines the decrease of hepatitis B incidence rate compared with previous studies. Even with a moderate prevalence, there may be a large reservoir of HCV and HBV-infected persons in Morocco, which indicates that many people are at risk of developing chronic liver disease related to viral hepatitis, added to the fact that antiviral therapy is not affordable by the vast majority of people in developing countries. Therefore, nosocomial risk prevention as well as health education among population are the main interventions that might help limiting the spread of these blood-borne infections.

                            Abbreviations

                            HBV: 

                            Hepatitis B virus

                            HCV: 

                            Hepatitis C virus

                            HBsAg: 

                            Hepatitis B surface antigen

                            Anti-HCV: 

                            Anti-HCV antibody

                            ELISA: 

                            Enzyme-linked immunosorbent assay

                            RIBA: 

                            Recombinant immunoblot assay

                            PCR: 

                            Polymerase chain reaction

                            CI: 

                            Confidence Interval

                            OR: 

                            Odds ratio.

                            Declarations

                            Acknowledgement

                            The authors would like to thank Sara Melville, Sonia Boughattas and Riham El sayed, for their thoughtful review of this manuscript.

                            Authors’ Affiliations

                            (1)
                            Molecular Biology Laboratory, Department of Medical Biology, Pasteur Institute of Morocco
                            (2)
                            Faculty of Science and Technology, Virology, Hygien & Microbiology Laboratory
                            (3)
                            Regional Blood Transfusion Center
                            (4)
                            Hematology Laboratory, Centre Hospitalier Universitaire Ibn Rochd

                            References

                            1. World Health Organization: Western Pacific regional plan for hepatitis B control through immunization. Philippines: Regional Office for the Western Pacific Manila; [http://​www.​wpro.​who.​int/​publications/​publications.​htm]. Accessed 5 January 2009
                            2. Lok AS, McMahon BJ: Chronic hepatitis B. Hepatology 2007, 45:507–539.PubMedView Article
                            3. Sood S, Malvankar S: Seroprevalence of Hepatitis B surface antigen, antibodies to the Hepatitis C virus, and human immunodeficiency virus in a hospital-based population in Jaipur, Rajasthan. Indian J Community Med 2010, 35:165–169.PubMedView Article
                            4. World Health Organization: Hepatitis C. [http://​www.​who.​int/​mediacentre/​factsheets/​fs164/​en]. Accessed 27 April 2009
                            5. Jian L, Yongdong Z, Xiaojing L, Yongzhen J, Ruiguang T, Yonghui Z, Jia W, Fengwei Z, Yong Z, Yue W, Shengli B: General epidemiological parameters of viral hepatitis A, B, C, and E in six regions of china: a cross-sectional study in 2007. PLoS One 2009, 4:e8467.View Article
                            6. Yoshizawa H: Hepatocellular carcinoma associated with hepatitis C virus infection in Japan: projection to other countries in the foreseeable future. Oncology 2002,62(Suppl. 1):8–17.PubMedView Article
                            7. Belbacha I, Cherkaoui I, Akrim M, Dooley KE, El Aouad R: Seroprevalence of hepatitis B and C among barbers and their clients in the Rabat region of Morocco. East Mediterr Health J 2011,17(12):911–919.PubMed
                            8. Zohoun A, Hadef R, Zahid H, Benkirane M: Seroprevalence of HBV and HCV in blood donors at the Blood Transfusion Center of Mohammed V Military Teaching Hospital in Rabat Morocco. Med Trop 2011,71(5):513–514.
                            9. Benouda A, Boujdiya Z, Ahid S, Abouqal R, Adnaoui M: Prevalence of hepatitis C virus infection in Morocco and serological tests assessment of detection for the viremia prediction. Pathol Biol 2009, 57:368–372.PubMedView Article
                            10. Rouabhia S, Malek R, Bounecer H, Dekaken A, Bendali Amor F, Sadelaoud M, Benouar A: Prevalence of type 2 diabetes in Algerian patients with hepatitis C virus infection. World J Gastroenterol 2010, 16:3427–31.PubMedView Article
                            11. Zaied A, Elneihoum A, Elzouki A: Routine screening for anti-HIV antibodies, hepatitis B surface antigen and anti-hepatitis C antibodies among general hospital in-patients. Jamahiriya Med J 2010, 8–21.
                            12. Frank C, Mohamed MK, Strickland GT, Lavanchy D, Arthur RR, Magder LS, El Khoby T, Abdel-Wahab Y, Aly Ohn ES, Anwar W, Sallam I: The role of parenteral antischistosomal therapy in the spread of hepatitis C virus in Egypt. Lancet 2000, 355:887–891.PubMedView Article
                            13. Cacoub P, Ohayon V, Sekkat S, Dumont B, Sbai A, Lunel F, Benslimane A, Godeau P, Archane MI: Epidemiologic and virologic study of hepatitis C virus infections in Morocco. Gastroenterol Clin Biol 2000,24(2):169–173.PubMed
                            14. Dubois F, Desenclos JC, Mariotte N, Goudeau A: Hepatitis C in a French population based survey, 1994: seroprevalence, frequency of viremia, genotype distribution and risk factors. Hepatology 1997, 25:1490–1496.PubMedView Article
                            15. Guadagnino V, Stroffolini T, Rapicetta M, Costantino A, Kondili LA, Menniti-Ippolito F, Caroleo B, Costa C, Griffo G, Loiacono L, Pisani V, Focà A, Piazza M: Prevalence, risk factors and genotype distribution of hepatitis C virus infection in the general population: a community based survey in southern Italy. Hepatology 1997, 26:1006–1011.PubMedView Article
                            16. Alter MJ, Margolis HS, Krawczynski K, Judson FN, Mares A, Alexander WJ, Hu PY, Miller JK, Gerber MA, Sampliner RE: The natural history of community-acquired hepatitis C in the United States. The sentinel counties chronic non-A, non-B hepatitis study team. N Engl J Med 1992, 327:1899–1905.PubMedView Article
                            17. Van Damme P, Thyssen A, Van Loock F: Epidemiology of hepatitis C in Belgium: present and future. Acta Gastroenterol Belg 2002, 65:78–79.PubMed
                            18. Centers for Disease Control and Prevention (CDC): Hepatitis C virus infection among adolescents and young adults: Massachusetts, 2002–2009. MMWR Morb Mortal Wkly Rep 2011,60(17):537–541.
                            19. Rantala M, van de Laar MJ: Surveillance and epidemiology of hepatitis B and C in Europe - a review. Euro Surveill 2008, 22:13(21).
                            20. Ayed Z, Houinato D, Hocine M, Ranger-Rogez S, Denis F: Prevalence of serum markers of hepatitis B and C in blood donors and pregnant women in Algeria. B Soc Pathol Exot 1995, 88:225–228.
                            21. Triki H, Said N, Ben Salah A, Arrouji A, Ben Ahmed F, Bouguerra A, Hmida S, Dhahri R, Dellagi K: Seroepidemiology of hepatitis B, C and delta viruses in Tunisia. Trans R Soc Trop Med Hyg 1997, 91:11–14.PubMedView Article
                            22. Yuen MF, Hou JL, Chutaputti A: Hepatocellular carcinoma in the Asia pacific region. Asia Pacific Working Party on Prevention of Hepatocellular Carcinoma. J Gastroenterol Hepatol 2009, 24:346–353.PubMedView Article
                            23. Lee HS, Han CJ, Kim CY: Predominant etiologic association of hepatitis C virus with hepatocellular carcinoma compared with hepatitis B virus in elderly patients in a hepatitis B endemic area. Cancer 1993, 72:2564–2567.PubMedView Article
                            24. Jung SH, Kim BH, Joung YH, Han YS, Lee BH, Dong SH, Kim HJ, Chang YW, Lee JI, Chang R: Clinical features of hepatocellular carcinoma in the 1990s. Korean J Gastroenterol 2003, 42:322–329.PubMed
                            25. Petrovic J, Salkic N, Ahmetagic S, Stojic V, MottDivkovic S: Prevalence of chronic hepatitis B and hepatitis C among first time blood donors in northeast Bosnia and Herzegovina: An estimate of prevalence in general population. Hepat Mon 2011, 11:629–633.PubMedView Article
                            26. Dutta S, Shivananda PG, Chatterjee A: Prevalence of hepatitis B surface antigen and antibody among hospital admitted patients in Manipal. Indian J Public Health 1994, 38:108–112.PubMed
                            27. Qamer S, Shahab T, Alam S, Malik A, Afzal K: Age-specific prevalence of hepatitis B surface antigen in pediatric population of Aligarh, North India. Indian J Pediatr 2004, 71:965–967.PubMedView Article
                            28. Ben Halima S, Bahri O, Maamouri N, Cheikh I, Alaya NB, Sadraoui A, Azaiez O, Azouz M, Mami NB, Triki H: Serological and molecular expression of Hepatitis B infection in patients with chronic Hepatitis C from Tunisia. North Africa. Virol J 2010, 15:7–229.
                            29. El-Sherif A, Abou-Shady M, Abou-Zeid H, Elwassief A, Elbahrawy A, Ueda Y, Chiba T, Hosney AM: Antibody to hepatitis B core antigen as a screening test for occult hepatitis B virus infection in Egyptian chronic hepatitis C patients. J Gastroenterol 2009, 44:359–364.PubMedView Article
                            30. Gaeta GB, Stornaiuolo G, Precone DF, Lobello S, Chiaramonte M, Stroffolini T, Colucci G, Rizzetto M: Epidemiological and clinical burden of chronic hepatitis B virus/hepatitis C virus infection. A multicenter Italian study. J Hepatol 2003, 39:1036–1041.PubMedView Article
                            31. Pontisso P, Ruvoletto MG, Fattovich G, Chemello L, Gallorini A, Ruol A, Alberti A: Clinical and virological profiles in patients with multiple hepatitis virus infections. Gastroenterology 1993, 105:1529–1533.PubMedView Article
                            32. Zarski JP, Bohn B, Bastie A, Pawlotsky JM, Baud M, Bost-Bezeaux F, Tran van Nhieu J, Seigneurin JM, Buffet C, Dhumeaux D: Characteristics of patients with dual infection by hepatitis B and C viruses. J Hepatol 1998, 28:27–33.PubMedView Article
                            33. Jardi R, Rodriguez F, Buti M, Costa X, Cotrina M, Galimany R, Esteban R, Guardia J: Role of hepatitis B, C, and D viruses in dual and triple infection: influence of viral genotypes and hepatitis B precore and basal core promoter mutations on viral replicative interference. Hepatology 2001, 34:404–410.PubMedView Article
                            34. Sobeslavsky O: Prevalence of markers of hepatitis B virus infection in various countries: a WHO Collaborative Study. Bull World Health Organ 1980,58(4):621–628.PubMed
                            35. Zahraoui-Mehadji M, Baakrim MZ, Laraqui S, Laraqui O, El Kabouss Y, Verger C, Caubet A, Laraqui CH: Infectious risks associated with blood exposure for traditional barbers and their customers in Morocco. Sante 2004,14(4):211–216.PubMed
                            36. Sbai A, Baha W, Ougabrai H, Allalia T, Dersi N, Lazaar F, Ennaji MM, Benjouad A, El Malki A, Hassar M, Benani A: Hepatitis B prevalence and risk factors in Morocco. Pathol Biol (Paris) 2012,60(5):e65-e69.View Article
                            37. Karaosmanoglu HK, Aydin OA, Sandikci S, Yamanlar ER, Nazlican O: Seroprevalence of hepatitis B: Do blood donors represent the general population? J Infect Dev Ctries 2012, 6:181–183.PubMed
                            38. Sbiti M, Bahji M, Zahid H, Benkirane M, Naji M, Bouhamidi B, El jouadi A: Prévalence des marqueurs sériques du virus de l’hépatite C chez une population de donneurs de sang. gaz transfus 2002, Juillet-aout:8–10.
                            39. Khmmaj A, Habas E, Azabi M: Frequency of hepatitis B, C, and HIV viruses among blood donors in Libya. Libyan J Med 2010, 5:5333.View Article
                            40. Palitzsch KD, Hottentrager B, Schollotmann K: Prevalence of antibodies against hepatitis C virus in the adult German population. Eur J Gastroenterol Hepatol 1999, 11:1215–1220.PubMedView Article
                            41. Mastouri M, Ben othman S, Bouzgarrou N, Hassin M, Pozzetto B, Trabelsi A, Khedhei M: Virus de l'hépatite C chez les donneurs de sang dans la région de Monastir (Tunisie): Prévalence et facteurs de risque. MHA 2004, 16:59–62.
                            42. Etard JF, Colbachini P, Dromigny JA: Hepatitis C antibodies among blood donors in Senegal. Emerg Infect Dis 2001, 9:1492–1493.View Article
                            43. Alter MJ, Kruszon-Moran D, Nainan OV: The prevalence of hepatitis C virus infection in the United States, 1988 through 1994. N Engl J Med 1999, 341:556–562.PubMedView Article
                            44. Muroz-Gomez R, Garcia-Monzon C, Garcia-Buey L: Hepatitis C virus infection in Spanish volunteer blood donors: HCV RNA analysis and liver disease. Eur J Gastroenterol Hepatol 1996, 8:273–277.View Article
                            45. Petrik J, Hewitt P, Barbara J, Allain J: Large scale HCV RNA screening in first time blood donors; the first step towards genomic screening of blood donations. HCV RNA screening study group. Vox Sang 1999, 76:159–162.PubMedView Article
                            46. Ghavanini AA, Sabri MR: Hepatitis B surface antigen and anti-hepatitis C antibodies among blood donors in the Islamic Republic of Iran. East Mediterr Health J 2000, 6:1114–1116.PubMed
                            47. Kim WR, Benson JT, Therneau TM, Torgerson HA, Yawn BP, Melton LJ: Changing epidemiology of hepatitis B in a US community. Hepatology 2004, 39:811–816.PubMedView Article
                            48. Pre-publication history

                              1. The pre-publication history for this paper can be accessed here:http://​www.​biomedcentral.​com/​1471-2458/​13/​50/​prepub

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