Seroprevalence of HBV and HIV co-infection in children and outcomes following highly active antiretroviral therapy (HAART) in Uyo, South-South Nigeria

Abstract

Background

Human Immunodeficiency Virus/Hepatitis B Virus (HIV/HBV) co-infection in Nigerian children has emerged as a major concern with the advent of HAART. Its impact on the immune system and liver has not been extensively studied in children.

Objectives

To determine the prevalence of HBV seropositivity among HIV positive children on HAART and its effect on immune response and liver enzymes.

Methods

All consecutive HIV positive children aged two months to seventeen years on HAART constituted the study population. Age and gender; CD4+ count, ALT, creatinine and HBsAg were tested and documented at enrolment and 12months.

Results

One hundred and seventy one patients were seen over this period. Seventy-two (43.4%) were males while 94 (56.6%) were females giving a male: female ratio of 1:1.3. The mean age of the patients was 63±43.4 months. Prevalence of HIV/HBV co-infection was 6.02% (95% CI 2.4–9.7). There was no significant effect of HBV status on elevation of ALT levels with 12 months of HAART. Co-infected patients had an odds ratio of achieving immune response of 0.14 (95% CI 0.02–0.79).

Conclusion

HIV/HBV co-infection rates in our children are comparable to other localities. ALT levels do not worsen with HAART and immune response of the co-infected children on HAART is lower.

Introduction

Nigeria has the greatest burden of paediatric HIV/AIDS in sub-Saharan Africa despite a national seroprevalence of 4.6%.^{1, 2} There are over 240,000 children living with HIV/AIDS, representing 15% of the African burden.³ The rate of vertical transmission is as high as 25%–42% in African countries. An estimated 600,000 new paediatric infections occur each year, with over 90% of these cases occurring in sub-Saharan Africa.⁴ Rapid progression of HIV-1 infection to Acquired Immune Deficiency Syndrome (AIDS) is also a major problem in these children. Up to 25% of prenatally infected infants progress to AIDS within one year and the remaining 75% within a median period of seven years.⁵

Nigeria belongs to the group of countries highly endemic for hepatitis B virus (HBV) infection,^{6, 7} a virus that shares common modes of transmission with HIV. ⁸ One of the major determinants of accelerated HIV disease progression is the presence of co-morbidities and opportunistic infections. The epidemiology, natural history and treatment of HIV co-infection with HBV has been studied extensively in adults^9–13 and documented sparingly in children,^14–16 more so among Nigerian children. In Tanzania and Cote d'Ivoire, the prevalence rates of the co-infection has been reported as 1.2%¹⁴ and 12.1%¹⁷ respectively while among Nigerian children, it is 8.3%.¹⁸

HBV infection is known to lead to chronic infection after the acute infection especially if acquired in the perinatal period and early childhood.^6,19 With improved survival due to the success of highly active antiretroviral therapy (HAART), chronic viral hepatitis has become a major source of co morbidity in HIV infected populations.²⁰ In adults, co-infection with HBV increases the risk for hepatotoxicity of HAART and likelihood of onset of an AIDS-defining illness, compared to infection with HIV-1 alone.²¹ It is not certain whether this is the case with children.

Most studies on co-infection in Nigeria have been in adults. With increasing access to HAART in Nigeria, it is expected that more HIV infected and co-infected children will survive. Although HIV coinfection with HBV has been recognised worldwide, there is limited data on the impact of this co-infection on the immune system. Data on its effect on the liver with HAART is also limited in developing countries like Nigeria. It is therefore imperative that the burden of this co-infection is quantified and its attendant effect investigated.

This study was therefore carried out to determine the prevalence of HBV seropositivity in a cohort of paediatric patients living with HIV/AIDS in a tertiary hospital in south-south Nigeria. The effect of co-infection on CD4+ lymphocytes and liver enzymes in the HAART era were also examined.

Methods

This prospective longitudinal study was conducted in the Infectious Disease Unit (IDU) of the Department of Paediatrics, University of Uyo Teaching Hospital (UUTH), Uyo, from December 2010 to August 2011. The hospital is the only tertiary and referral centre in Uyo, capital city of Akwa Ibom State of Nigeria. It is also the main centre for Paediatric HIV care. It serves the 3.9 million population of the State.

The study was approved by the University of Uyo Teaching Hospital Research and Ethics Committee.

The IDU runs a weekly Paediatric HIV/AIDS clinic. It is one of the President's Emergency Plan Funds for AIDS Relief (PEPFAR) sites where antiretroviral drugs are given and investigations are carried out at no cost to the patient. The baseline investigations that are conducted before commencement of HAART include CD4+ count, full blood count, electrolytes, creatinine, urea, and liver function tests. Eligibility criteria for commencement of HAART included all children less than 24 months irrespective of the CD4+ cell count; CD4+ cell count < 750 in children aged 25 months to 59 months, < 350 for 60 months and above and any child seen at clinical stage 3 or 4.

Eligible patients were commenced on HAART and were seen on a regular basis at the clinic. HAART comprised at least two drugs from the Nucleoside reverse transcriptase inhibitor (NRTIs) class of antiretroviral drugs and one from the Nonnucleoside reverse transcriptase inhibitor class (NNRTIs). The first line drugs used included Lamivudine (3TC), Zidovudine (AZT) and Nevirapine (NVP) as fixed dose combination. At follow up visits, they received general paediatric care with full physical examination and anthropometric measurements taken. Their CD4+ counts and full blood count were monitored on a 3-monthly basis, while electrolytes, creatinine, urea and liver function tests were monitored biannually. All consecutive children aged two months to seventeen years that were confirmed to be HIV positive during the study period were enrolled.

Informed consent was obtained from the parent/guardian prior to enrolment. Children older than 10 years also gave a verbal consent. Confirmation was by enzyme — linked immunosorbent assay (ELISA) in those older than 18months or by DNA polymerase chain reaction (PCR) for those younger than 18 months. HIV RNA viral load and HBV DNA viral load were not done as our facility didn't have the equipment for these tests at the time of the study.

All children that were not eligible for HAART (five in all) were excluded from subsequent analysis after the prevalence of co-infection among the HIV positive was obtained. CD4+ cell count and HBsAg tests were done at enrolment and one week after if they were eligible for HAART, and baseline investigations were carried out. Thereafter, the patients had an average of three adherence counselling sessions within a period of two weeks before initiation of HAART.

Demographic information (age and sex), results of investigations (CD4+ count, alanine aminotransferase, and creatinine) were obtained and documented.

HBsAg was tested using First Response Rapid HBsAg test (Blumber B. S. 1991, San Diego, USA). For CD4+ count, Flow Cytometry using Partec cyflow counter (Greve, B. Et al 2003, Germany) was used. All the chemistry was done using the in vitro quantitative analysis method using Vitros DT 60 11 chemistry system (Johnson & Johnson). All assay protocols, cut-offs and interpretation were according to the manufacturer's instructions.

A gender comparison of the clinical, biochemical characteristics and HBV prevalence of the participants was done. The prevalence of HBV in each of the age groups was also explored. The proportion of those with elevated ALT levels (> 2 times upper limit of reference range for our laboratory which was 70 iu/l ) by co-infection status was computed and univariate and multivariate logistic regression models were used to investigate the effect of HBV status on having elevated serum ALT at commencement of HAART. Immune response was defined as the achievement of at least 50 cells/µL increments in CD4 count from baseline at 12 months of therapy. The effect of co-infection on achieving immune response was also investigated using multivariate logistic regression. All factors with a p-value of the Wald statistic < 0.25 at univariate analysis or known to have potential effect on immune response were included in the multivariate model built using stepwise regression.

Results

One hundred and sixty six (166) paediatric patients were seen over this period. Seventy - two (43.4%) were males while 94 (56.6%) were females giving a male:female ratio of 1:1.3. The mean age of the patients was 63 ± 43.4 months. The mean duration on Highly active antiretroviral therapy (HAART) was 24.2±18.1 months. Table 1 shows the baseline characteristics of the study participants. Those aged 2– 23 months were 30 (18.1%), 24 ‒ 60 months were 67 (40.4 %), 61 ‒ 120 months 48 (28.9%) and > 120 months were 21 (12.6%).

Table 1.

Gender distribution of baseline characterisitics

	Total	Male	Female	p - value
Age	63.0±43.4	61.9±41.1	64.3±46.4	0.75
ALT (U/L)	42 (31 – 58)	38.5 (29 – 56)	45 (34 – 60)	0.12*
Creatinine (umol/L)	44.5±20.1	44.5±20.7	44.4±19.3	0.98
Baseline CD4 count(cells/uL)	503 (233 – 860)	468 (232 – 822)	591.5 (264.5 – 957)	0.44*

^*Wilcoxon rank sum test.

Prevalence of HIV-HBV co-infection

Ten (6.02%) (95% CI 2.4 to 9.7% ) of the patients had HIV - HBV co-infection. There was no significant difference in the prevalence of HBV in both genders. Four (5.8%) of the females were HBV positive compared to 6 (6.7%) of the males, p = 0.54. With regards to age groups, the highest prevalence was found in the 10 years group (11.5%), followed by the 5 – 10 years age group (9.3% ). There was no association between age and HBV co -infection (p=0.47). A comparison of the sociodemographic and clinical characteristics of those with HIV-HBV co-infection with those with only HIV infection is shown in Figure 1 and table 2. Individuals with HBV co-infection had higher serum creatinine levels and lower CD4 cell counts at baseline and at 12 months of therapy.

Figure 1.

Graph box showing CD4 count by HBV status

Table 2.

Comparison of sociodemographic and clinical characteristics by HBV status

	Hepatitis B status		p - value
	Negative	Positive
Male gender (n/%)	83 (56.1)	6 (60)	0.81
Age (months)	61.8±42.5	83.9±49.9	0.12
ALT (U/L)	42 (31 – 56)	50 (30 – 70)	0.49
Creatinine (umol/L)	42.5 (32 – 50)	54.5 (45 – 56)	0.02
CD4 count at baseline (cells/uL)	529 (249 – 861)	149 (53 – 232)	0.0003
CD4 count at 6 months of HAART	893 (560 – 1245)	318 (83 – 566)	0.0004

Influence of Hepatitis B status on ALT levels

At the commencement of HAART, 66 (39.8%) of the children had elevated serum ALT levels; (70% of the co-infected children and 58.1% of the HIV only group ) but this difference was not statistically significant (p = 0.46). Only four of the children had ALT levels greater than two times the upper limit of normal and all were Hepatitis B negative. A multivariate logistic regression model did not show any significant effect of HBV status on development of elevated ALT levels one year after commencement of HAART (see table 3). However, male gender appeared to be protective against having elevated ALT levels and those with elevated ALT levels at commencement of HAART were more prone to developing higher ALT levels while on therapy.

Table 3.

Association between elevated ALT level and HBV status

	Univariate	Multivariate
	Odds ratio (95%) CI,	Odds ratio (95%) CI,
	p - value	p - value
Positive HBV status	1.74 (0.48 – 6.29) 0.40	0.97 (0.08 – 12.58) 0.98
Male gender	0.14 (0.07 – 0.29) <0.001	0.01 (0.002 – 0.07) <0.001
Age (months)	1.00 (0.99 – 1.01) 0.94	0.99 (0.97 – 1.01) 0.33
CD4 count at baseline (100 cells/UL)	0.99 (0.98 – 1.00) 0.24	0.98 (0.97 – 0.99) 0.048
Serum creatinine (umol/L)	1.00 (0.98 – 1.02) 0.58	1.00 (0.97 – 1.04) 0.11
ALT (U/L)	1.11 (1.07 – 1.15) <0.001	1.17 (1.10 – 1.24) <0.001

^*The area under the Receiver Operator Characteristic (ROC) Curve of the model was 0.82

Influence of HBV/HIV co-infection on immune response

Seventy percent of the co-infected and 84.5% of the mono-infected patients achieved immune response at 12 months of therapy. A second logistic regression model was used to assess the effect of HBV/HIV co-infection on achievement of immune response. The findings are summarized in Table 4. Those with HIV/HBV co-infection have an odds ratio of achieving immune response of 0.14 (95% CI 0.02 – 0.79) after correcting for CD4 count at baseline, age, gender, BMI, ALT and serum creatinine levels.

Table 4.

Univariate and Multivariate logistic models for predictors of immune response

	Univariate	Multivariate*
	Odds ratio (95%CI) p-value	Odds ratio (95%CI) p-value
Positive HBsAg	0.43 (0.10 – 1.78) 0.24	0.14 (0.02 – 0.79) 0.03
CD4/100 cells/µL	0.98 (0.97 – 0.99) <0.001	0.98 (0.97 – 0.99)
Female gender	0.95 90.41 – 2.21) 0.91	0.58 (0.20 – 1.66) 0.31
ALT (U/L)	1.01 (0.99 – 1.03) 0.25	1.01 (0.98 – 1.03) 0.54
BMI	1.01 (0.84 – 1.21) 0.93	1.08 (0.85 – 1.35) 0.58
Age (months)	1.01 (0.99 – 1.02) 0.25	1.00 (0.99 – 1.02) 0.65
Creatinine (µmol/L)	0.99 (0.97 – 1.01) 0.26	0.98 (0.96 – 1.01) 0.16

^* The area under the Receiver Operator Characteristic (ROC) Curve of the model was 0.80

Discussion

HAART has transformed HIV/AIDS from a uniformly fatal illness into a manageable chronic infection and has been shown to be able to restore CD4+ cells in HIV infected patients. ²² The gains of HAART could be compromised by co-infection with hepatitis viruses as they are known to have adverse effects on the prognosis of HIV and hepatitis infections. ²³ Consequently, increased attention has to be paid to co-infection of hepatitis viruses and HIV.

In this study, the HIV/HBV co-infection rate of 6.02% is comparable to the 7.7% and 8.3% obtained from other Nigerian studies.^18,24 It is however lower than the 12.1%¹⁷ from a neighbouring west African country of Cote d' Ivoire but higher than rates of 1.2%¹⁴ and 4%¹³ from some east African countries. A study from Bronx, New York reported a prevalence of 2.6%.¹⁶ These differences may reflect the seroprevalent rates of HBsAg in the different populations. Although some Nigerian studies quoted HBsAg rates as high as 44.7%, the inclusion of Hepatitis B vaccine in the National Programme on Immunization (NPI) in the past decade has reduced the population prevalence and consequently reduced the HIV/HBV co-infection prevalence.

The finding that the mono and co-infected patients shared similar demographic characteristics with respect to age and sex was also reported by other authors. ^{14, 16, 24} The mean age of the co-infected patients, however, was higher in this study. The Bronx, New York study also identified more adolescents to be co-infected. This may be attributed to the fact that children in this age group were exposed before the current prevention strategies were available( inclusion of HBV in the NPI schedule in 2004). In contrast, Sadoh and coworkers²⁴ concluded that immunization did not make any significant difference in the prevalence of co-infection. This conclusion, however, is presumptuous because they analysed only the hepatitis B immunization history of the under-five instead of the whole study population.

The higher level of the liver enzyme, alanine aminotransferase (ALT) in the co-infected group was also reported by other workers.^{14, 16} This is expected since hepatitis viruses are known to elevate liver enzymes.²⁶ We found no association between HAART and elevated ALT. This is similar to the findings of Telatela et al ¹⁴ and Toussi et al ¹⁶ but contrasts reports from other studies. ^27–29 Our patients were on first line regimen which comprises lamivudine, zidovudine and nevirapine. It has been reported that lamivudine as a component of HAART, has a beneficial effect in that it causes inhibition of HBV replication in adherent patients⁸. Other drugs that have this beneficial effect are tenofovir and emtricitabine³⁰. On the contrary, patients on protease inhibitors are at risk of developing a worsening of the liver disease since they are associated with more risk of elevated ALT than other antiretroviral drugs. ²⁹

As reported by other authors^{14, 16} in their study of paediatric patients, our co-infected patients had significantly lower CD4+ cell counts compared to the mono-infected group. However, these authors did not study the effect of HAART on the CD4 cell count. We noted that the co-infected patients were less likely to achieve immune response even with HAART for one year. This calls for establishment of a treatment protocol for HIV/HBV co-infected patients which includes at least two of the antiretroviral drugs that induce suppression of HBV replication, as first line regimen. This will reduce the hepatotoxic effect of the viruses, improve immune response as well as prevent development of resistance on prolonged use of lamivudine alone.

In contrast, in the adult population, Lincoln and co-workers³¹ on behalf of the Australian HIV Observational Database, reported that co-infection with HBV did not appear to influence CD4 count recovery following commencement of HAART. Their work involved a larger group of participants (2089) and the immune response was also checked after 12 months of HAART. Our study appears to be the first to examine this issue in Nigerian children.

Conclusion

We have demonstrated that co-infection of HIV with HBV exists in our local at rates that are comparable with those of other communities. We have also shown that HAART does not worsen ALT levels and that the immune response of the co-infected patients is lower with treatment compared to the mono-infected patients.

Recommendations

We therefore recommend that screening for HBsAg be mandatory in all paediatric HIV patients in our environment, especially the adolescents. They should receive special attention with regards to, the antiretroviral drugs they are treated with, monitoring and follow up to assess disease progression.

The limitations of this study include the inability of our laboratory to carry out HIV RNA viral load and the HBV DNA viral load. Further studies with determination of viral loads are advocated.