Skip to main content
  • Research note
  • Open access
  • Published:

Epidemiology of viral hepatitis in the Republic of Congo: review

Abstract

Objective

Considered an endemic zone, Republic of Congo has a high seroprevalence rate of hepatitis B and C virus. To know the extent of hepatitis infection as a public health problem, we reviewed published literature and other sources for reports of these viral infections in the country.

Results

High seroprevalence of HBV and HCV carriage in blood donors were observed in studies confirming Congo’s place in the hyperendemic area of HBV and HCV infection. These prevalence were compared by Chi square test. We compared the prevalence of three studies conducted in 1996, 2015 and 2016. The statistical results were very significant. HBV genotype E was most prevalent. Very few studies were done on pregnant women. Difficulties in the care and management of patients were also noted because of the high cost of often unavailable treatments. Difficulties arise, however, when an attempt was made to implement the National Hepatitis Control Program. Despite studies conducted on hepatitis prevalence, health interventions are still needed to care and manage these patients and the need to implement the national hepatitis control is more pressing in the Congo.

Introduction

Viral hepatitis is caused by five types of viruses (A, B, C, D and E) that are transmitted differently [1]. Type A and E are transmitted through food and water [2]. Infection with these viruses can lead to epidemic outbreaks of hepatitis in populations without safe drinking water and in poor sanitation conditions [3,4,5]. These two types of hepatitis (A and E) do not cause infection or chronic liver disease and do not require specific treatment [6, 7]. Types B and C are infections transmitted by blood during injection or medical interventions performed in poor sanitary conditions [8,9,10,11]. Hepatitis B virus is also transmitted sexually [12,13,14]. There is also transmission from mother to the child [15,16,17,18] which turns out to be the most important in the Congo, where pregnant women were found with significant proportions of hepatitis markers [19, 20].

Considered an endemic zone, Congo has a high seroprevalence rate of hepatitis C virus. A study conducted in 2014 among 17,351 blood donors, in the two major cities of the country revealed that the relative frequency was 4.1% in Brazzaville and 4.3% in Pointe-Noire [21]. At Brazzaville, the seroprevalence rate among 1363 blood donors was documented to be 9.9%. Hepatitis B infection remains also a public health problem in Congo [22].

To appreciate the extent of hepatitis infection as a public health problem in Republic of Congo, we reviewed published literature and other sources for reports of viral hepatitis in the country. The objective of this review is to report the overall prevalence of viral hepatitis in the Republic of Congo.

Methods

Main text

Although there is no comprehensive report on viral hepatitis in ROC, all studies focusing on hepatitis in the ROC have been considered. PubMed database was used to retrieve research articles about viral hepatitis in ROC. The search terms were: ((“hepatitis”[MeSH Terms] OR “hepatitis”[All Fields] OR “hepatitis a”[MeSH Terms] OR “hepatitis a”[All Fields]) AND (“congo”[MeSH Terms] OR “congo”[All Fields])) NOT (Democratic [All Fields] AND Republic [All Fields] AND (“congo”[MeSH Terms] OR “congo”[All Fields]).

Criteria of inclusion

This review considered full articles and abstracts published in peer review journals between 1952 up to 2016 which have reported incidence and prevalence of viral hepatitis in Republic of Congo.

Target population

Most studies on hepatitis in the Republic of Congo reported on blood donors. So our conclusion will be made based on blood donors.

Strategy

Data were extracted and verified in full by one author (GLLS) on the following: country, year of publication, year of collection; study type, study design, biomarkers tested, study population, sample size, proportion male, age, HCV seroprevalence, PCR test based prevalence, genotype, subtypes.

Analysis data

After collecting the related information, the data were transferred into the computer and analyzed by EpiInfo version 7.1.1. Data were analyzed using descriptive statistical methods, Chi square and correlation at a significant level of < .05.

Results

We retrieved 16 research articles from the PubMed database. We excluded 7 articles from this review because their content did not mention any subtype. Table 1 summarizes the description of studies on hepatitis in the Republic of Congo.

Table 1 Description of selected studies

Localisation of studies

Most of the studies were conducted in Brazzaville and Pointe-Noire and one study was conducted in several localities: Niari, Bouenza, Lekoumou among ethnic groups (Bantu et Pygmy) [23].

Hepatitis: a public health concern

In Congo, many people carry the virus B and/or C [19,20,21,22]. However, most of them are unaware of this, believing that the only chronic viral disease is HIV/AIDS [24, 25]. This situation is exacerbated by the lack of a response strategy that incorporates specific awareness-raising actions [26,27,28]; co-infection with hepatitis viruses and HIV/AIDS [29], the low or non-existence of immunization coverage against the B virus [30,31,32,33] or a lack of knowledge of HIV status, even among health workers [34, 35]. In addition, the difficulties in caring and management of patients were also noted because of the high cost of often unavailable treatments. Vaccines are available to prevent hepatitis B at a cost of 27,000 FCFA for adults and 9000 FCFA for the child for three doses [36], vaccination is the best way to get immunity to these viruses [37,38,39,40].

Effective drugs are available, but treatment remains inaccessible to many patients because of its high cost. In the Republic of Congo, hepatitis C treatment costs about one million FCFA per month and lasts at least 1 year. For hepatitis B, there is no treatment as such in the country. Treatment is now being done using antiretrovirals for HIV control that also act on hepatitis B [41, 42]. The screening costs is currently 30,000 FCFA and the full biological testing is of the order of 450,000–500,000 FCFA [36].

Epidemiology of viral hepatitis

Hepatitis B

The high incidence of HBsAg carriage in blood donors was observed in the Pointe-Noire, Niari and Bouenza departments, confirming Congo’s place in the hyperendemic area of HBV infection. Atipo-Ibara et al. [22] in their study observed the frequence of HBsAg carriage in blood donors in few localities of the country: Pointe-Noire (10.8%), Nkayi (9.3%), Dolisie (8.9%), Madingou (5.9%) and Mouyondzi (5.2%) [22].

Angounda et al. [19] indicated a prevalence of HBeAg was 15.3 and 73% of patients were anti-HBe positive. In this study Angounda et al. detected the Chronic HBV among 111 patients at high risk of hepatitis disease progression. And the presence of HBeAg was high in chronic active hepatitis (CAH) (41.18%) and HBeAb positive was higher in the age group 39–45 year with a prevalence of 56.7% [43].

The prevalence of serological markers of hepatitis B was higher in the study of Angounda et al. among 648 blood donors in Brazzaville, which confirms the high risk of blood transfusion [44]. Over all, although the prevalence of hepatitis B was different from one study to another (see Table 2), this prevalence especially for HBsAg was above 6%, which is considered high.

Table 2 Summary of the prevalence of hepatitis B according to selected studies and biomarkers

Hepatitis C

Central Africa is considered as a high-prevalence region of anti-HCV antibodies, detected in about 2–20% of the population [45,46,47]. In ROC, HCV seroprevalence studies have been conducted among blood donors [23, 48, 49] or carried out among the Bantu and Pygmy populations. And HCV seroprevalence was lower in Pygmies (3.8%) [23]. The similarly study demonstrated a low prevalence of HCV infection among pygmies living in Cameroon [50].

In the previous study conducted in 2014 in Pointe-Noire, seroprevalence of anti-HCV antibodies in the blood donors has been reported to 4.7% [48].

The last study conducted among adults in one HIV clinic in the capital, Brazzaville in 2010, showed that the prevalence of HCV antibody was 5.7%. Studies have revealed that the majority of HCV positive patients were predominantly male [21, 51].

The key problem with this explanation is that generally, blood donors are male [52] and there are multiple restrictions for blood donation by women [53], which are linked either to breastfeeding [54, 55], menstruation [56] or pregnancy [57].

Genotyping of hepatitis

Hepatitis B

In the single study on the genotyping of hepatitis B in the Republic of Congo, 82 samples out of 111 (73.9%) were genotyped in the HBV S region. Of these, 58 (70.7%) subjects were infected with HBV genotype E and 24 (29.3%) were infected with HBV genotype A. Previously in Cameroon, the two prevalent genotypes identified were 69.6% HBV genotype E and 30.4% HBV genotype A among the HIV-1 infected patients [58]. HBV genotype E was also the most prevalent genotype in Angola, found in 87.5%, followed by genotype A in 10% [59]. Genotypes E and A are the most prevalent among blood donors in areas of high endemicity [43].

Hepatitis C

In the study conducted by Cantaloube et al. in 2010, the genotyping was performed through amplification and sequencing of a 339 pb amplicon located from position 8370 to 8708 in the NS5b region and a 357-nucleotide sequence located from position 1029 to 1385 in the E1 region. The results of this study showed 21 strains belonged to characterized subtypes, that is 4c in 8 (25.8%), 4h in 2 (6.5%), 4k in 3 (9.7%), and 4r in 8 (25.8%) [23]. The most common subtypes were 4c and 4r. All these subtypes were identified in a study conducted in DRC [60].

Atipo-ibara et al. used only the NS5B region, they obtained sequencing of 17 samples, 16 genotypes 4 (G4) and 1 genotype 2 (G2) [22]. The distribution of genotype 4 subtypes in this article shows great genetic diversity and predominance of one subtype G4. The epidemic history of HCV subtype 4c and 4r slowed considerably [23]. Similarly genetic diversity has been observed in Kinshasa in DRC by Iles et al. in 2013 and 2015 [60,61,62]. Zeba et al. in 2014 in Burkina Faso observed that HCV genotype 4 was the least frequent among the blood donors [63].

Risk factors for hepatitis B and C

Blood transfusion remains the most important mode of transmission of hepatitis C [64, 65]. In the Republic of Congo, Elira et al. in 2003 reported the seroprevalence of anti-HCV antibodies among 252 multitransfused patients to be 1.7% [49]. In one of their previous study they observed a prevalence of 6.7% of anti-HCV antibodies in blood donors [51]. Atipo Ibara et al. in 2013 on the other side indicated that blood transfusion was a risk factor in 143 donors out of a total of 1363 (10.5%) donors [22].

Thus, such as HIV/AIDS, hepatitis C is a major concern in blood transfusion services that requires mandatory pre-transfusion screening [49, 66]. ELISA is the most common routine test for hepatitis C screening [67,68,69]. The risk of false positive reactions that are due to cross-reactions with other viruses is very common [70, 71].

Global response: implementation of the national program for the control of viral hepatitis B and C

A strategic plan was drawn for 2016–2021 and has to be implemented [72, 73]. It focuses on public awareness and prevention as well as access to safe, affordable and effective care and treatment [74, 75]. One of the goals of this strategy is to reduce the number of new cases of chronic hepatitis by 30% by 2020 and 90% by 2030 [76, 77] and to reduce mortality rates due to hepatitis B and C by 10% by 2020 and by 65% by 2030 [78].

So far in the Congo, a short term national program for the control of viral hepatitis B and C drawed since 2014 could not assure affordability of drugs and the care of patients remained very costly in the country [36, 79]. The national program will be responsible for regular supply of medicines biological tests necessary for the care and management of patients suffering from hepatitis. This program will play an important role in the collection of statistical data in the Republic of Congo.

Difficulties arise, however, when an attempt was made to implement the National Hepatitis Control Program. The few studies conducted in ROC showed that, there were the unmet needs for routine HBsAg screening and implementation of immunization against HBV as effective means to prevent hepatitis B [22]. New strategies must be developed to include routine screening of pregnant women and implementation of vaccination programs for newborns [43].

Conclusion

Hepatitis is a major health problem that requires greater attention in Republic of Congo.

Although prevalence vary from one study to another, this prevalence was high, above 6% for HBsAg, one of the most reliable markers for hepatitis B infection. Also, genotype B was the most prevalent. This review reports finding of significant public health importance revealing a high frequency of co-infection with HBV/HCV in HIV infected individuals in Congo with risk factors for co-infection in the population. This review also stress that blood to be transfused should undergo systematic analyses in order to exclude viral infections including hepatitis.

Limitations

In this study we summarized insights of hepatitis virus; pathology which is not well explored in our country. This review based finding of previous studies; data incompleteness and poor document retention system were limitation of this study.

Abbreviations

HBV:

Hepatitis B Virus

HCV:

Hepatitis C Virus

ROC:

Republic of Congo

References

  1. Franca R, Silva L, Melo MC, Cavalcante S, Lima B, Rocha A, et al. Pediatric knowledge about acute viral hepatitis. Braz J Infect Dis. 2004;8:361–6.

    Article  Google Scholar 

  2. Teshale EH, Hu DJ, Holmberg SD. The two faces of hepatitis E virus. Clin Infect Dis. 2010;51:328–34.

    Article  PubMed  Google Scholar 

  3. Franco E, Meleleo C, Serino L, Sorbara D, Zaratti L. Hepatitis A: epidemiology and prevention in developing countries. World J. Hepatol. 2012;4:68.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Hakim ST, Afaque F, Javed S, Kazmi SU, Nadeem SG. Microbial agents responsible for diarrheal infections in flood victims: a study from Karachi, Pakistan. Open J Med Microbiol. 2014;4:106–14.

    Article  Google Scholar 

  5. Kamal SM, Mahmoud S, Hafez T, El Fouly R. Viral hepatitis A to E in South Mediterranean countries. Mediterr J Hematol Infect Dis. 2010. http://www.mjhid.org/article/view/5424. Accessed 27 May 2017.

  6. Matheny SC, Kingery Do JE. Hepatitis A. Am Fam Physician. 2012;86:1027–34.

    PubMed  Google Scholar 

  7. Péron JM. Hepatitis E virus infection and cirrhosis of the liver. Gastroenterol Hepatol. 2016;12(9):565–7.

    Google Scholar 

  8. Hosoglu S, Celen M, Geyik M, Soyoral Y, Kara I. Transmission of hepatitis C by blood splash into conjunctiva in a nurse. Am J Infect Control. 2003;31:502–4.

    Article  PubMed  Google Scholar 

  9. Jafari S, Copes R, Baharlou S, Etminan M, Buxton J. Tattooing and the risk of transmission of hepatitis C: a systematic review and meta-analysis. Int J Infect Dis. 2010;14:e928–40.

    Article  PubMed  Google Scholar 

  10. Seo DH, Whang DH, Song EY, Han KS. Occult hepatitis B virus infection and blood transfusion. World J Hepatol. 2015;7:600.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Yuen M-F, Ka-Ho Wong D, Lee C-K, Tanaka Y, Allain J-P, Fung J, et al. Transmissibility of hepatitis B virus (HBV) infection through blood transfusion from blood donors with occult HBV infection. Clin Infect Dis. 2011;52:624–32.

    Article  PubMed  Google Scholar 

  12. Handsfield HH. Hepatitis A and B immunization in persons being evaluated for sexually transmitted diseases. Am J Med. 2005;118:69–74.

    Article  Google Scholar 

  13. Lin AWC, Sridhar S, Wong KH, Lau SKP, Woo PCY. Epidemiology of sexually transmitted viral hepatitis in human immunodeficiency virus-positive men who have sex with men in Asia. J Formos Med Assoc. 2015;114:1154–61.

    Article  PubMed  Google Scholar 

  14. Terrault NA, Dodge JL, Murphy EL, Tavis JE, Kiss A, Levin TR, et al. Sexual transmission of hepatitis C virus among monogamous heterosexual couples: the HCV partners study. Hepatology. 2013;57:881–9.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Indolfi G, Azzari C, Resti M. Perinatal transmission of hepatitis C virus. J Pediatr. 2013;163(1549–1552):e1.

    Google Scholar 

  16. Liu Y, Wen J, Chen J, Xu C, Hu Y, Zhou Y-H. Rare detection of occult hepatitis B virus infection in children of mothers with positive hepatitis B surface antigen. PLoS ONE. 2014;9:e112803.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Ranger-Rogez S, Alain S, Denis F. Hepatitis viruses: mother to child transmission. Pathol Biol (Paris). 2002;50:568–75.

    Article  CAS  PubMed  Google Scholar 

  18. Verghese VP, Robinson JL. A systematic review of hepatitis E virus infection in children. Clin Infect Dis. 2014;59:689–97.

    Article  PubMed  Google Scholar 

  19. Angounda BM, Bokilo Dzia A, Boumba LMA, Itoua C, Ahombo G, Moukassa D, et al. Prevalence of serologic markers and risk factors for hepatitis B virus among pregnant women in Brazzaville. Congo Int J Sci Res IJSR. 2016;5:1907–12.

    Google Scholar 

  20. Itoua-Ngaporo A, Sapoulou M, Ibara J, Iloki L, Denis F. Prevalence of hepatitis B viral markers in a population of pregnant women in Brazzaville (Congo). J Gynecol Obstet Biol Reprod. 1994;24:534–6.

    Google Scholar 

  21. Atipo-Ibara BI, Mimesse J, Bokilo-Dzia A, Deby-Gassaye Ahoui-Apendi C, Bossali F, et al. Virus de l’hépatite C: étude des génotypes au Congo (Brazzaville). J Afr Hépato-Gastroentérol. 2014;8:16–9.

    Article  Google Scholar 

  22. Atipo-Ibara BI, Itoua-Ngaporo AN, Dzia-Lepfoundzou A, Ahoui-Apendi C, Deby-Gassaye C, Bossali F, et al. Virus de l’hépatite B au Congo (Brazzaville): séroprévalence et diversité génétique chez les donneurs de sang en zones hyper endémiques. J Afr Hépato-Gastroentérol. 2015;9:127–31.

    Article  Google Scholar 

  23. Cantaloube J-F, Gallian P, Bokilo A, Jordier F, Biagini P, Attoui H, et al. Analysis of hepatitis C virus strains circulating in Republic of the Congo: HCV in Republic of the Congo. J Med Virol. 2010;82:562–7.

    Article  PubMed  Google Scholar 

  24. Kwak YE. Lack of awareness of hepatitis B infection status and risk of developing hepatic complications in the us population. Gastroenterology. 2017;152:S162.

    Google Scholar 

  25. Siddiqui MA, Ansari S, Alam Khan Q. Socio-Demographic profile of patients with hepatitis B and hepatitis C infections at Maswasi, Uttar Pradesh. Middle East J Rehabil Health. 2017 (In Press). http://www.jrehabilhealth.com/?page=article&article_id=44359. Accessed 29 May 2017.

  26. Locarnini S, Hatzakis A, Chen D-S, Lok A. Strategies to control hepatitis B: public policy, epidemiology, vaccine and drugs. J Hepatol. 2015;62:S76–86.

    Article  PubMed  Google Scholar 

  27. Mesquita F, Santos ME, Benzaken A, Corrêa RG, Cattapan E, Sereno LS, et al. The Brazilian comprehensive response to hepatitis C: from strategic thinking to access to interferon-free therapy. BMC Public Health. 2016;16. http://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-016-3784-4. Accessed 29 May 2017.

  28. Shiferaw F, Letebo M, Bane A. Chronic viral hepatitis: policy, regulation, and strategies for its control and elimination in Ethiopia. BMC Public Health. 2016;16. http://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-016-3459-1. Accessed 29 May 2017.

  29. de Oliveira SB, Merchan-Hamann E, Amorim LDAF. HIV/AIDS coinfection with the hepatitis B and C viruses in Brazil. Cad Saúde Pública. 2014;30:433–8.

    Article  PubMed  Google Scholar 

  30. Bekondi C, Zanchi R, Seck A, Garin B, Giles-Vernick T, Gody JC, et al. HBV immunization and vaccine coverage among hospitalized children in Cameroon, Central African Republic and Senegal: a cross-sectional study. BMC Infect Dis. 2015;15. http://bmcinfectdis.biomedcentral.com/articles/10.1186/s12879-015-1000-2. Accessed 29 May 2017.

  31. Hennessey K, Mendoza-Aldana J, Bayutas B, Lorenzo-Mariano KM, Diorditsa S. Hepatitis B control in the World Health Organization’s Western Pacific Region: targets, strategies, status. Vaccine. 2013;31:J85–92.

    Article  PubMed  Google Scholar 

  32. Musa B, Samaila A, Femi O, Borodo M, Bussell S. Prevalence of hepatitis B virus infection in Nigeria, 2000–2013: a systematic review and meta-analysis. Niger J Clin Pract. 2015;18:163.

    Article  CAS  PubMed  Google Scholar 

  33. Ropero Álvarez AM, Pérez-Vilar S, Pacis-Tirso C, Contreras M, El Omeiri N, Ruiz-Matus C, et al. Progress in vaccination towards hepatitis B control and elimination in the Region of the Americas. BMC Public Health. 2017;17. http://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-017-4227-6. Accessed 29 May 2017.

  34. Cherutich P, Kaiser R, Galbraith J, Williamson J, Shiraishi RW, Ngare C, et al. Lack of knowledge of HIV status a major barrier to HIV prevention, care and treatment efforts in Kenya: results from a nationally representative study. PLoS ONE. 2012;7:e36797.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Mohlabane N, Tutshana B, Peltzer K, Mwisongo A. Barriers and facilitators associated with HIV testing uptake in South African health facilities offering HIV Counselling and Testing. Health SA Gesondheid. 2016;21:86–95.

    Article  Google Scholar 

  36. Agence d’information d’Afrique Centrale. Lutte contre les hépatites virales B et C : les médecins de Pointe-Noire souhaitent la mise en place d’un programme national. 2014. http://www.adiac-congo.com/content/lutte-contre-les-hepatites-virales-b-et-c-les-medecins-de-pointe-noire-souhaitent-la-mise–3. Accessed 29 Jan 2016.

  37. Ciupe SM, Ribeiro RM, Perelson AS. Antibody responses during hepatitis B viral infection. PLoS Comput Biol. 2014;10:e1003730.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Halliday J, Klenerman P, Barnes E. Vaccination for hepatitis C virus: closing in on an evasive target. Expert Rev Vaccines. 2011;10:659–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Lauer GM. Immune responses to hepatitis C virus (HCV) infection and the prospects for an effective HCV vaccine or immunotherapies. J Infect Dis. 2013;207:S7–12.

    Article  CAS  PubMed  Google Scholar 

  40. Leuridan E, Van Damme P. Hepatitis B and the need for a booster dose. Clin Infect Dis. 2011;53:68–75.

    Article  PubMed  Google Scholar 

  41. Hill A, Khoo S, Fortunak J, Simmons B, Ford N. Minimum costs for producing hepatitis C direct-acting antivirals for use in large-scale treatment access programs in developing countries. Clin Infect Dis. 2014;58:928–36.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Rajbhandari R, Chung RT. Treatment of hepatitis B: a concise review. Clin Transl Gastroenterol. 2016;7:e190.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Angounda BM, Ngouloubi GH, Dzia AB, Boumba LMA, Baha W, Moukassa D, et al. Molecular characterization of hepatitis B virus among chronic hepatitis B patients from Pointe Noire, Republic of Congo. Infect Agent Cancer. 2016;11. http://infectagentscancer.biomedcentral.com/articles/10.1186/s13027-016-0088-3. Accessed 20 May 2017.

  44. Angounda B, Bokilo Dzia A, Niama FR, Ahombo G, Mboumba LMA, Moukassa D, et al. Seroprevalence of markers and risk factors of hepatitis B virus among blood donors in Brazzaville. Congo Int J Innov Sci Res. 2016;20:171–9.

    Google Scholar 

  45. Luma HN, Eloumou SAFB, Malongue A, Temfack E, Noah DN, Donfack-Sontsa O, et al. Characteristics of anti-hepatitis C virus antibody-positive patients in a hospital setting in Douala. Cameroon Int J Infect Dis. 2016;45:53–8.

    Article  PubMed  Google Scholar 

  46. Njouom R, Caron M, Besson G, Ndong-Atome G-R, Makuwa M, Pouillot R, et al. Phylogeography, risk factors and genetic history of hepatitis C virus in Gabon. Central Africa. PLoS ONE. 2012;7:e42002.

    Article  CAS  PubMed  Google Scholar 

  47. Vannata B, Zucca E. Hepatitis C virus-associated B-cell non-hodgkin lymphomas. Hematology. 2014;2014:590–8.

    Article  PubMed  Google Scholar 

  48. Alidjinou EK, Moukassa D, Ebatetou-Ataboho E, Mahoungou GH, Pambou J-P, Sané F, et al. Higher levels of hepatitis C virus RNA found in blood donors co-infected with HIV as compared to HCV mono-infected donors. J Infect Dev Ctries. 2014;8. http://www.jidc.org/index.php/journal/article/view/4767. Accessed 22 May 2017.

  49. Dokekias EA, Okandze-Elenga JP, Gouary Kinkouna AS, Bokilo Dzia Lepfoundzou A, Garcia S. Séroprévalence de l’hépatite virale C chez les malades polytransfusés au CHU de Brazzaville. Bull Soc Pathol Exot. 2003;96:279–82.

    PubMed  Google Scholar 

  50. Foupouapouognigni Y, Mba SAS, a Betsem EB, Rousset D, Froment A, Gessain A, et al. Hepatitis B and C virus infections in the three pygmy groups in Cameroon. J Clin Microbiol. 2011;49:737–40.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Dokekias EA, Okandze Elenga J, Manya Okanga D, Dzia-Lepfoundzou A. Prévalence des marqueurs viraux moyens chez les donneurs de sang à Brazzaville. Transf Clin Biol. 2001;8:84–9.

    Google Scholar 

  52. Erhabor O, Adias TC. Essentials of blood transfusion science. Author House UK. March 2013. pp 528.

  53. Danic B, Bigey F. Les contre-indications au don du sang. Impact de l’arrêté du 12 janvier. Transfus Clin Biol. 2009;2009(16):209–13.

    Article  Google Scholar 

  54. Prados Madrona D, Fernández Herrera MD, Al E. Women as whole blood donors: offers, donations and deferrals in the province of Huelva, south-western Spain. Blood Transfus. 2014. http://www.bloodtransfusion.it/articolo.aspx?idart=002601&idriv=90. Accessed 4 June 2017.

  55. Wambach K, Riordan J. Breastfeeding and human lactation. Burlington: Jones & Bartlett Publishers, University of Kansas School of Nursing Karen Wambach; 2014.

    Google Scholar 

  56. Dauar ET, Patavino GM, Mendrone Júnior A, Gualandro SFM, Sabino EC, de Almeida-Neto C. Risk factors for deferral due to low hematocrit and iron depletion among prospective blood donors in a Brazilian center. Rev Bras Hematol E Hemoter. 2015;37(5):306–15.

    Article  Google Scholar 

  57. Organization Pan American Health. Eligibility for blood donation: recommendations for education and selection of prospective blood donors. Washington, DC: Pan American Health Organization; 2009.

    Google Scholar 

  58. Magoro T, Gachara G, Mavhandu L, Lum E, Kimbi HK, Ndip RN, et al. Serologic and genotypic characterization of hepatitis B virus in HIV-1 infected patients from South West and Littoral Regions of Cameroon. Virol J. 2016;13. http://virologyj.biomedcentral.com/articles/10.1186/s12985-016-0636-x. Accesssed 22 May 2017.

  59. Valente F, Lago BV, Castro CAV, Almeida AJ, Gomes SA, Soares CC. Epidemiology and molecular characterization of hepatitis B virus in Luanda. Angola. Mem Inst Oswaldo Cruz. 2010;105(8):970–7.

    Article  PubMed  Google Scholar 

  60. Iles JC, Abby Harrison GL, Lyons S, Djoko CF, Tamoufe U, Lebreton M, et al. Hepatitis C virus infections in the Democratic Republic of Congo exhibit a cohort effect. Infect Genet Evol. 2013;19:386–94.

    Article  PubMed  Google Scholar 

  61. Iles JC, Raghwani J, Harrison GLA, Pepin J, Djoko CF, Tamoufe U, et al. Phylogeography and epidemic history of hepatitis C virus genotype 4 in Africa. Virology. 2014;464–465:233–43.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Iles JC, Njouom R, Foupouapouognigni Y, Bonsall D, Bowden R, Trebes A, et al. Characterization of hepatitis C virus recombination in Cameroon by use of nonspecific next-generation sequencing. J Clin Microbiol. 2015;53:3155–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Zeba M, Sanou M, Bisseye C, Kiba A, Nagalo B, Djigma F, et al. Characterisation of hepatitis C virus genotype among blood donors at the regional blood transfusion centre of Ouagadougou, Burkina Faso. Blood Transfus. 2014;12:s54.

    PubMed  PubMed Central  Google Scholar 

  64. Chen SL, Morgan TR. The natural history of hepatitis C virus (HCV) infection. Int J Med Sci. 2006;3:47–52.

    Article  PubMed  PubMed Central  Google Scholar 

  65. Westbrook RH, Dusheiko G. Natural history of hepatitis C. J Hepatol. 2014;61:S58–68.

    Article  PubMed  Google Scholar 

  66. Dzia-Lepfoundzou A, Angounda BM, Niama FR, Gambicky R, Oko APG, Okoko AR, et al. Suivi sérologique d’une cohorte d’enfants transfusés au CHU de Brazzaville, Congo. J Med Health Sci. 2017;18.

  67. Bajpai M, Gupta E, Choudhary A. Hepatitis C virus: screening, diagnosis, and interpretation of laboratory assays. Asian J Transfus Sci. 2014;8:19.

    Article  PubMed  PubMed Central  Google Scholar 

  68. Marwaha N, Sachdev S. Current testing strategies for hepatitis C virus infection in blood donors and the way forward. World J Gastroenterol. 2014;20:2948.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Rouet F, Deleplancque L, Mboumba BB, Sica J, Mouinga-Ondémé A, Liégeois F, et al. Usefulness of a fourth generation ELISA assay for the reliable identification of HCV infection in HIV-positive adults from Gabon (Central Africa). PLoS ONE. 2015;10:e0116975.

    Article  PubMed  PubMed Central  Google Scholar 

  70. Ioniţă E, Lupulescu E, Alexandrescu V, Chiriţă C, Bălteanu M, Neguţ AE. False-positive ELISA reactions for the hepatitis C virus and the human immunodeficiency virus after anti-influenzal vaccination. Bacteriol Virusol Parazitol Epidemiol Buchar Rom. 1990;1995(40):249–52.

    Google Scholar 

  71. Mullis CE, Laeyendecker O, Reynolds SJ, Ocama P, Quinn J, Boaz I, et al. High frequency of false-positive hepatitis C virus enzyme-linked immunosorbent assay in Rakai, Uganda. Clin Infect Dis. 2013;57:1747–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Seale A, Broutet N, Narasimhan M. Assessing process, content, and politics in developing the global health sector strategy on sexually transmitted infections 2016–2021: implementation opportunities for policymakers. PLOS Med. 2017;14:e1002330.

  73. WHO. Regional action plan for the implementation of the global health sector strategy on viral hepatitis 2017–2021 [Internet]. Cairo: WHO Regional Office for the Eastern Mediterranean: WHO; 2017 p. 34. Available from: http://apps.who.int/iris/bitstream/10665/258729/1/EMROPUB_2017_EN_19931.pdf.

  74. FitzSimons D, Hendrickx G, Hallauer J, Larson H, Lavanchy D, Lodewyckx I, et al. Innovative sources for funding of viral hepatitis prevention and treatment in low- and middle-income countries: a roundtable meeting report. Hepatol Med Policy. 2016;1. http://hmap.biomedcentral.com/articles/10.1186/s41124-016-0022-8. Accessed 29 May 2017.

  75. WHO. By 2030, viral hepatitis to be eliminated from the African Region. Media Center;2016. http://www.afro.who.int/en/media-centre/pressreleases/item/8921-by-2030-viral-hepatitis-to-be-eliminated-from-the-african-region.html.

  76. Easterbrook PJ, Roberts T, Sands A, Peeling R. Diagnosis of viral hepatitis. Curr Opin HIV AIDS. 2017;12:302–14.

    Article  PubMed  PubMed Central  Google Scholar 

  77. WHO. Global health sector strategies on HIV, viral hepatitis and sexually transmitted infections (STIs) 2016–2021. 2015.

  78. WHO. Combating hepatitis B and C to reach elimination by 2030. Geneva: WHO; 2016. p. 1–24. http://apps.who.int/iris/bitstream/10665/206453/1/WHO_HIV_2016.04_eng.pdf.

  79. Vox LE. Gouvernement annonce un programme national de lutte contre les hépatites. 2016. http://www.vox.cg/gouvernement-annonce-programme-national-de-lutte-contre-hepatites/. Accessed 29 Jan 2016.

  80. Taty-Taty R, Yala F, Courouce AM, Arthaud ML, Saliou P, Biendo M, et al. [Carrier state for HBs antigen and HBc antibody in Brazzaville (congo): sero-epidemiological study in the hospital and nonhospital environment]. Bull Soc Pathol Exot. 1990;83:149–54.

  81. Bossali F, Taty-Taty R, Houssissa P, N’suele W, Lingouala LG, Ontsira EN, et al. Séroprévalence de la coinfection hépatite B, hépatite C et VIH chez des femmes accouchées à la maternité de l’hôpital Adolphe Sicé de Pointe-Noire en 2010. J Afr Hépatol Gastroentérol. 2012;6(4):315–9.

  82. Bossali F, Koumou Okandze L, Katende S, Thouassa A. Séroprévalence de l’hépatite B chez les malades atteints de cirrhose et des malades porteurs du carcinome hépatocellulaire à Pointe-Noire de 2005 à 2008. J Afr d'Hépato-Gastroentérologie 2011;5(1):2.

  83. Makuwa M, Bakouetela J, Bassindikila A, Samba-Lefebvre. Étude des marqueurs sérologiques de l’hépatite B chez les patients congolais testés pour l’infection à VIH. Médecine Afr. Noire. 1996;43.

Download references

Authors’ contributions

LSGL conceived of the idea for the paper and edited the draft extensively. CNN analysed the data, revised the manuscript. Both authors read and approved the final manuscript.

Authors’ information

Laure Stella Ghoma Linguissi is Searcher at Institut National de Recherche en Sciences de la Santé (IRSSA), in Brazzaville. She led this review for looking for data on hepatitis in Republic of Congo.

My goal in developing this review was to assist my country in reaching its objectives public health in the development of National Hepatitis Program.

Acknowledgements

There was no source of funding for this manuscript. The authors would like to thank Dr. Mathew Bates for proofreading assistance.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The data that support the findings of this review are available from [19, 49] but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of Taty-Taty et al. ‎(1990) and Atipo-Ibara et al. [21, 22].

Consent to publish

Not applicable.

Ethics approval and consent to participate

The Ethics Committee for Health Sciences Research (CERSSA) has found that as it is a literary review study of previous research studies that had already obtained ethical approval it was not necessary to solicit a ethical approval. No participants’ consent could be obtained, as it was a review study.

Funding

The authors alone are responsible for the content and writing of the paper. They benefited from no source of funding or sponsorship, either from the public, private or not-for-profit sectors. The corresponding author had full access to all data in the study and had final responsibility to submit on behalf of all authors this manuscript for publication.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in institutional affiliation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Laure Stella Ghoma Linguissi.

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

Ghoma Linguissi, L.S., Nkenfou, C.N. Epidemiology of viral hepatitis in the Republic of Congo: review. BMC Res Notes 10, 665 (2017). https://doi.org/10.1186/s13104-017-2951-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13104-017-2951-8

Keywords