Treatment Penetration and Correlates of Diagnostic Parameters among Hepatitis B Seropositive individuals in Ondo State, Nigeria

Main Article Content

MS Odimayo
BY Alabi
WO Adebimpe
SI Nwadioha
OA Olatunji
BO Ogedengbe

Abstract

Our aim is to determine Hepatitis B Virus (HBV) infection's treatment penetration among infected patients and levels of correlation between serologic, biochemical and molecular tests. Serologic tests considered were, Hepatitis B surface Antigen (HBsAg), Hepatitis B surface Antibody (HBsAb), Hepatitis B 'e' Antigen (HBeAg), Hepatitis B core Antibody (HBcAb) and Hepatitis B 'e' Antibody (HBeAb); biochemical tests included alanine transaminase (ALT) and the molecular test was HBV viral DNA load. These parameters were considered among Hepatitis B seropositive patients so as to evaluate individual relevance of these tests to disease management in an endemic population. In this retrospective study, data of patients who attended Viral Hepatitis Clinics in University of Medical Sciences Teaching Hospital Complex, Ondo, Nigeria from 2014 to 2019 were extracted. Serological profiles (HBsAg, HBsAb, HBeAg, hepatitis B core antibody; HBcAb), antibody against HBeAg (HBeAb); biochemical markers (alanine transaminase; ALT); and HBV viral DNA loads were collated. Data were analyzed using the Statistical Package for Social Sciences (SPSS) software version 23.0. Among a total of 630 HBsAg sero-positive patients, 48 completed the three series of tests and commenced treatment; giving a treatment penetration rate of 7.6%. Among these, 28 were males and 20 were females (1.4:1) with mean age of 34years. All had detectable viral load above 20 iu/mL and were all HBcAb positive; 26 (54.2%) had viral load below 2,000 iu/mL. Among the total of 48 patients 2 were HBeAg positive while 46 were negative. Among 46 which were HBeAg seronegative, 20 (43.5%) had viral load above 2,000 iu/mL. The 2 patients with HBeAg had viral load above 20,000 iu/mL and were also positive for HBeAb. Among the 19 (39.6%) which had ALT values greater than 20iu/L, nine (47.4%) had viral load above 2,000 iu/mL, while among 29 (60.4%) with ALT below 20 iu/L, 13 (44.8%) had viral load greater than 2,000iu/L. We concluded that wide gaps exist between HBsAg sero-positivity and treatment penetration in our environment. Neither serology, ALT nor viral loads can single handedly predict needs for patients' treatment. The presence of HBeAb was not protective against HBeAg. The need for special national hepatitis programs for adequate provision of treatment and follow-up services cannot be overemphasized.

Metrics

Metrics Loading ...

Article Details

How to Cite
1.
Odimayo M, Alabi B, Adebimpe W, Nwadioha S, Olatunji O, Ogedengbe B. Treatment Penetration and Correlates of Diagnostic Parameters among Hepatitis B Seropositive individuals in Ondo State, Nigeria. Wes J Med Biomed Sci [Internet]. 2022 Feb. 13 [cited 2024 Nov. 24];3(1):107-13. Available from: https://wjmbs.com.ng/index.php/wjmbs/article/view/78
Section
Original Article

References

Lesi OA, Audu RA, Okwuraiwe AP, Adeleye OO, Ige FA, Iwuorah JC((2019)). Serologic and virologic markers of Nigerian patients with hepatitis B infection. Niger J Clin Pract, 22:534- 538

Adebola TO, Akin O, Balogun MS, Ajudua A, Nguku P (2016), Seroprevalence of Hepatitis B infection in Nigeria: A national survey. Am J Trop Med Hygiene, 95:902

Odimayo MS, Nwokedi EOP, Nwadioha SI, Araoye MA (2010). Prevalence of Hepatitis B Seropositivity among adults in Makurdi, Nigeria. Mary Slessors Jou rnal of Medicine and Medical Sciences, 10 (2):1-5.

Mathai F, Otieno NM, Muturi K S, Kalebi A, Lihana R(2017). Correlation of Quantitative Assay of HBsAg and Hepatitis B Virus DNA Levels Among Chronic HBV Patients Attending Pathologist Lancet Laboratory in Nairobi, Kenya, Arch Clin Infect Dis, 12(4):13306. doi: 10.5812/archcid.13306

Makuza, JD, Rwema, JOT, Ntihabose, CK et al((2019)). Prevalence of hepatitis B surface antigen (HBsAg) positivity and its associated factors in Rwanda. BMC Infect Dis, 19: 381. https://doi.org/10.1186/s12879-019-4013-4)

Alavian SM, Miri SM (2011). Dilemma of HBsAg seroconversion in chronic hepatitis B infection: Dilemma of HBsAg in chronic HBV. Hepat Mon,11:6768.[PMC free] [Google Scholar]

Alavian SM (2012). Occult hepatitis B virus infection among hemodialysis patients. Hepat Mon, 12:242243. [PMC free article] [PubMed] [Google Scholar]

World Health Organization 2015. Guidelines for the prevention, care and treatment of persons with chronic hepatitis B infection. Available from: www.who.int/hepatitis/publications/hepatitis-b-guidelines/en/

Sarin SK, Kumar M, Lau GK, et al (2016). Asian-Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update. Hepatol Int, 10:198.

European Association for the Study of the Liver (EASL)( 2017). Clinical Practice Guidelines on the management of hepatitis B virus infection. J Hepatol, 67:370398.

Nwadioha IS , Odimayo S, Ene BC , Oghagbon KE, Utoo P , Nwannadi A(2018) . Missed serologic diagnosis of hepatitis b virus infection among blood donors in Benue State University Teaching Hospital, Makurdi, Nigeria. Microbiol Res J Internl, 25(6):1-8

Odaibo GN, Ola OS, Olaleye OD (2013). Hepatitis B Virus DNA in Patients with HBsAg in South Western Nigeria. J Med Virol, 85 (2) :214-8

World Health Organization(2019). Initiative for vaccine research https://www.who.int/news-room/fact-sheets/detail/hepatitis-b

Atay AE, Seven G, Yalcin K, PS, Degertekin H. (2012). Evaluation of hepatitis B viraemia levels in patients with HBeAg-negative chronic hepatitis B virus infection. J Int Med Res; 40 (5):1891-1896. doi:10.1177/030006051204000529.

Huw P. David D, Tamale Z, Tobias V, Michael., Cissy K. et al (2017). Hepatitis B serological markers and plasma DNA concentrations. AIDS, 31(8): 11091117.

Odimayo MS, Nwadioha SI, Nwokedi E P (2013). Prevalence of HBeAg among Hepatitis B seropositive individuals in Makurdi Nigeria. American Journal of Biological , Chemical and Pharmacologic Sciences, 1(8):90-95.

Papatheodoridis, GV and Hadziyannis, SJ. (2001), Diagnosis and management of pre‐core mutant chronic hepatitis B. Journal of Viral Hepatitis, 8: 311-321. doi:10.1046/j.1365- 2893.2001.00303.x)

World Health Organization (WHO). Global Hepatitis report 2017. Available from: www.who.int/entity/hepatitis/publications/global-hepatitis-report2017/en/- 30k. [Last accessed on 2017 Sep 4],

Bárcena Marugán, R., & García Garzón, S. (2009). DNA-guided hepatitis B treatment, viral load is essential, but not sufficient. World journal of gastroenterology, 15(4), 423430. https://doi.org/10.3748/wjg.15.423.

Jabbar K, Niamatullah K, Atta UR, Shahid NK , Hamidullah S (2016). Biochemical and Molecular Characterization of Hepatitis B Virus in Dera Ismail Khan Division. Journal of Health Science, 6(4): 62-66.

Kew, MC. (2013), Hepatitis viruses (other than hepatitis B and C viruses) as causes of hepatocellular carcinoma: an update. J Viral Hepat, 20: 149-157. https://doi.org/10.1111/jvh.12043.

Tatsuo K, Taichiro G, Yosuke H, Mitsuhiko M, Masao O. (2019) Molecular Mechanisms Driving Progression of Liver Cirrhosis towards Hepatocellular Carcinoma in Chronic Hepatitis B and C Infections: A Review. Int J Mol Sci. 20(6): 1358. Published online 2019 Mar 18. doi: 10.3390/ijms20061358

Most read articles by the same author(s)