MATERNAL TRANSMISSION OF
HEPATITIS B VIRUS (HBV)
IN TRIPOLI-LIBYA

Hamida El-Magrahe, Abdul Rahaman
Furarah, Kheiria El-Figih, Suad El Urshfany
and Khalifa Sifaw Ghenghesh
Faculty of Sciences, Tripoli University;
Faculty of Medicine, Tripoli University; and
Tripoli Medical Center; Tripoli-Libya
Introduction
• Family
– Hepadnaviridae

• Genus
– Orthohepadnavirus

• Transmission
– Blood, and Blood products.
– Sexual contact.
– Vertical transmission.
Perinatal transmission of HBV
• Time of transmission.
• Factors determining perinatal
transmission.
Table 1. Serological markers of HBV infection
Phase

AntiAntiHBsAg HBs HBeAg HBe

AntiHBc

HBV
DNA

Acute

+

-

+

-

IgM

+

Chronic
active

+

-

+

-

IgG

+

Chronic
carrier

+

-

-

+

IgG

-

Recovery

-

+

-

+

IgG

-

Vaccine

-

+

-

-

-

-
Factors determining transmission of
HBV
• Acute hepatitis B infection during
pregnancy.
– Women having acute hepatitis B in the
first or second trimester rarely transmit
HBV to their neonates
• risk of transmission is low 3%.

– Women having acute hepatitis B in the
last trimester of pregnancy
• risk of transmission is about 70-78%.
Factors determining transmission of
HBV
• Chronic hepatitis B infection during
pregnancy.
– HBsAg+ve and HBeAg+ve
• risk of transmitting HBV to their neonates is
80-90 %
• 85-90 % of infected infants become chronic
carriers.

– HBsAg+ve, HBeAg-ve, and anti-HBe-ve
• risk of transmitting HBV to their neonates is
31%.

– HBsAg-ve, HBeAg-ve, and anti-HBe+ve
• risk of transmitting HBV to their neonates is
10-20 %.
Objectives of the Study
• Pregnant women with HBV are a major
reservoir of the virus in the community.
– To estimate the prevalence of HBV
infection among pregnant women.
– To assess the importance of maternal
transmission of HBV.
– To define the importance of different HBV
markers in the transmission of the virus
from mother to the fetus.
Materials and Methods
• Blood samples from 1500 pregnant
women (aged <21 to >35 years
[mean=28yr]) and 1500 cord blood of
their neonates at Tripoli Medical Center,
Tripoli were tested for the different
markers of HBV using ELISA
techniques.
• The study was carried out between April
2001 and March 2002.
Results
• HBsAg was detected in 23 (1.5%) pregnant women
and in 14 (0.9%) neonates.
• Although HBsAg was detected at higher rate in
pregnant women aged >25 years (1.8% [22/1235])
than in pregnant women aged <25 years (0.4%
[1/265]), the difference was not statistically significant
(P>0.05, Chi-squares test).
• All HBsAg+ve neonates were born to HBsAg+ve
mothers with a rate of maternal transmission at
60.9% [14/23].
• HBeAg was detected in 21.7% (5/23) and 7.1 (1/14) of
HBsAg+ve pregnant women and HBsAg+ve neonates,
respectively.
• HBV markers detected in pregnant women and
neonates are shown Table 2.
Table 2. Prevalence of HBV serological markers
in pregnant women and their neonates
No. (%) positive
Serological
marker

Pregnant
women
(n=1500)

Neonates
(n=1500)

HBsAg

23 (1.5)

14 (0.9)

HBeAg

5 (0.3)

1 (<0.1)

Anti-HBe

11 (0.7)

8 (0.5)

Total-antiHBc

16 (1.1)

9 (0.6)

Anti-HBcIgM

4 (0.3)

7 (0.5)
Table 3. Hepatitis B status of 1500 Libyan pregnant women
Hepatitis B Virus serological markers

Group

Maternal status

I
II

No. (%)
Positive

HBeAg

Anti-HBe

Susceptible

-

-

-

-

-

1477 (98.5)

Early infection,
asymptomatic

+

-

-

-

-

2 (0.12)

+

-

+

-

-

1 (0.06)

Acute infection,
replicating

+

+

+

+

-

3 (0.2)

Recovery or
convalescence?

+

+

-

-

+

7 (0.5)

+

-

-

-

+

4 (0.25)

Chronic infection

V

Anti-HBcIgM

Recovery or
convalescence?

VI

Anti-HBcTotal

Acute infection

III

HBsAg

+

+

-

-

-

4 (0.25)

Chronic Infection,
replicating

+

+

-

+

-

2 (0.12)
Conclusions
• This study showed high rate (>60%) of
maternal transmission of HBV among
HBsAg+ve mothers in Tripoli.
• Because of the high risk of developing chronic
HBV infection at birth among infants born to
HBsAg+ve mothers, administration of HBIG
in combination with hepatitis B vaccine as
post-exposure prophylaxis for such infants is of
paramount importance.
• In addition, universal HBsAg screening of all
pregnant women will greatly assist in reducing
the maternal transmission of HBV in the
country.

Maternal transmission of HBV-Libya

  • 1.
    MATERNAL TRANSMISSION OF HEPATITISB VIRUS (HBV) IN TRIPOLI-LIBYA Hamida El-Magrahe, Abdul Rahaman Furarah, Kheiria El-Figih, Suad El Urshfany and Khalifa Sifaw Ghenghesh Faculty of Sciences, Tripoli University; Faculty of Medicine, Tripoli University; and Tripoli Medical Center; Tripoli-Libya
  • 2.
    Introduction • Family – Hepadnaviridae •Genus – Orthohepadnavirus • Transmission – Blood, and Blood products. – Sexual contact. – Vertical transmission.
  • 3.
    Perinatal transmission ofHBV • Time of transmission. • Factors determining perinatal transmission.
  • 4.
    Table 1. Serologicalmarkers of HBV infection Phase AntiAntiHBsAg HBs HBeAg HBe AntiHBc HBV DNA Acute + - + - IgM + Chronic active + - + - IgG + Chronic carrier + - - + IgG - Recovery - + - + IgG - Vaccine - + - - - -
  • 5.
    Factors determining transmissionof HBV • Acute hepatitis B infection during pregnancy. – Women having acute hepatitis B in the first or second trimester rarely transmit HBV to their neonates • risk of transmission is low 3%. – Women having acute hepatitis B in the last trimester of pregnancy • risk of transmission is about 70-78%.
  • 6.
    Factors determining transmissionof HBV • Chronic hepatitis B infection during pregnancy. – HBsAg+ve and HBeAg+ve • risk of transmitting HBV to their neonates is 80-90 % • 85-90 % of infected infants become chronic carriers. – HBsAg+ve, HBeAg-ve, and anti-HBe-ve • risk of transmitting HBV to their neonates is 31%. – HBsAg-ve, HBeAg-ve, and anti-HBe+ve • risk of transmitting HBV to their neonates is 10-20 %.
  • 7.
    Objectives of theStudy • Pregnant women with HBV are a major reservoir of the virus in the community. – To estimate the prevalence of HBV infection among pregnant women. – To assess the importance of maternal transmission of HBV. – To define the importance of different HBV markers in the transmission of the virus from mother to the fetus.
  • 8.
    Materials and Methods •Blood samples from 1500 pregnant women (aged <21 to >35 years [mean=28yr]) and 1500 cord blood of their neonates at Tripoli Medical Center, Tripoli were tested for the different markers of HBV using ELISA techniques. • The study was carried out between April 2001 and March 2002.
  • 9.
    Results • HBsAg wasdetected in 23 (1.5%) pregnant women and in 14 (0.9%) neonates. • Although HBsAg was detected at higher rate in pregnant women aged >25 years (1.8% [22/1235]) than in pregnant women aged <25 years (0.4% [1/265]), the difference was not statistically significant (P>0.05, Chi-squares test). • All HBsAg+ve neonates were born to HBsAg+ve mothers with a rate of maternal transmission at 60.9% [14/23]. • HBeAg was detected in 21.7% (5/23) and 7.1 (1/14) of HBsAg+ve pregnant women and HBsAg+ve neonates, respectively. • HBV markers detected in pregnant women and neonates are shown Table 2.
  • 10.
    Table 2. Prevalenceof HBV serological markers in pregnant women and their neonates No. (%) positive Serological marker Pregnant women (n=1500) Neonates (n=1500) HBsAg 23 (1.5) 14 (0.9) HBeAg 5 (0.3) 1 (<0.1) Anti-HBe 11 (0.7) 8 (0.5) Total-antiHBc 16 (1.1) 9 (0.6) Anti-HBcIgM 4 (0.3) 7 (0.5)
  • 11.
    Table 3. HepatitisB status of 1500 Libyan pregnant women Hepatitis B Virus serological markers Group Maternal status I II No. (%) Positive HBeAg Anti-HBe Susceptible - - - - - 1477 (98.5) Early infection, asymptomatic + - - - - 2 (0.12) + - + - - 1 (0.06) Acute infection, replicating + + + + - 3 (0.2) Recovery or convalescence? + + - - + 7 (0.5) + - - - + 4 (0.25) Chronic infection V Anti-HBcIgM Recovery or convalescence? VI Anti-HBcTotal Acute infection III HBsAg + + - - - 4 (0.25) Chronic Infection, replicating + + - + - 2 (0.12)
  • 12.
    Conclusions • This studyshowed high rate (>60%) of maternal transmission of HBV among HBsAg+ve mothers in Tripoli. • Because of the high risk of developing chronic HBV infection at birth among infants born to HBsAg+ve mothers, administration of HBIG in combination with hepatitis B vaccine as post-exposure prophylaxis for such infants is of paramount importance. • In addition, universal HBsAg screening of all pregnant women will greatly assist in reducing the maternal transmission of HBV in the country.