|
Prevalence
of Hepatitis C in Healthy Population and Patients with Liver Ailments in
Myanmar
Khin Pyone Kyi*, Myo Aye*, Khin May Oo*,
Moh Moh Htun*,
San San Oo*,
Khin Ohnmar Lwin* and Khin Maung Win**
|
Abstract
Hepatitis C Virus (HCV) infection is one
of the major blood-borne infections worldwide and HCV carriers may develop
chronic hepatitis leading to liver cirrhosis and hepatocellular
carcinoma (HCC). In this study, a total of 741 Myanmar subjects were
tested for evidence of hepatitis C infection by RIBA Immunoblot
Assay 3 from Chiron Company, USA. In the 362
apparently healthy subjects, 9(2.5%) were positive for antibody to HCV
(anti-HCV), whereas in the 379 patients with various types of liver
diseases, approximately 25% were positive for the HCV marker. The
prevalence of HCV infection among these two study groups with respect to
age, sex, history of exposure to blood or surgical operation and different
types of liver diseases were also determined. This study brought to light
the association of HCV infection with liver cirrhosis and hepatocellular carcinoma in Myanmar.
|
Introduction
TRANSMISSION of hepatitis C virus (HCV) occurs through blood and
blood products, although sexual transmission and intrafamilial transmission have also been reported.1
HCV is responsible for most cases of post transfusion hepatitis, but there is
epidemiological evidence to suggest that it is a cause of acute hepatitis
without overt blood exposure and has been labelled
community-acquired or sporadic HCV infection. The incidence of chronic sequelae is high and approximately 70% of patients with
post transfusion hepatitis C will develop chronic hepatitis. A high
percentage of these patients will progress onto cirrhosis and hepato-cellular carcinoma (HCC).2
In HCV infection, the antigenaemia is
limited and the concentration of HCV antigens in serum are at the lower limit
of detectability by existing immunoassay technology. 3
At present, the diagnosis of HCV infections are mostly carried out by viral
antibody (anti-HCV) tests. A positive anti-HCV test indicates exposure to HCV and represents therefore, a surrogate marker of ongoing infection.4
A polymerase chain reaction (PCR) has been used to detect HCV RNA but is
difficult both to interpret and perform.
A study conducted in 1991 at the Department of Medical Research
(DMR), Myanmar reported that among the HCC cases, 35% were positive for
anti-HCV, detected by using Anti-C100-3 EIA test kits using Enzyme
Linked Immunosorbent Assay test system (ELISA) from Orthodiagnostic Systems, USA.5
The present study was undertaken with an aim to determine the prevalence of
HCV infection among apparently healthy subjects and patients with various
liver diseases by using immunoblot assay system to
detect the HCV antibody.
Materials and methods
Subjects
The study consisted of 741 subjects which included 362
apparently healthy subjects without liver disease who were enrolled for
hepatitis B vaccination at the DMR. The remaining 379 subjects were patients
with various types of liver diseases attending the out-patient department of the
Liver Unit at the YangonGeneralHospital. These included
patients with fatty liver, acute hepatitis, chronic hepatitis, cirrhosis and
HCC already confirmed by standard tests. Blood was collected from the
subjects, and after serum separation, the samples were stored at -80°C until
ready to be tested for anti-HCV.
Test system
Chiron RIBA HCV Test System - Immunoblot
Assay 3.0 from USA, a qualitative
enzyme immunoassay nitrocellulose based confirmatory test for anti-HCV was
used to detect the hepatitis C marker in the 741 serum samples.
Results
In the apparently healthy 362 subjects, the prevalence of
anti-HCV was 9(2.5%) whereas in the 379 patients with various types of liver
diseases, 95 patients (25%) were positive for the HCV marker.
Percentages of the HCV marker varied in patients with different
types of liver diseases. In the 36 patients with fatty liver, anti-HCV was
not detected. Only 10% were positive for anti-HCV in 30 acute hepatitis
patients whereas 15(17.2%) were positive in 87 chronic hepatitis patients,
38.5% in the 117 cirrhosis patients and 29.3% in 109 hepatocellular
carcinoma patients.
The detection of anti-HCV in the above-mentioned two groups of
subjects according to sex was evident as follows. In the subjects without
liver disease, 100% of 177 male subjects were negative for the HCV marker
whilst in the 185 female subjects, 4.86% were positive. In the liver disease
patients, 22.3% were positive in 242 male patients and 29.9% were positive in
137 female patients.
The prevalence rate of anti-HCV became higher according to age
in both groups. In this study, anti-HCV was not detected below the age of 21
years. Between the ages of 21 to 50 years, the prevalence of the HCV marker
was 1.1% to 2.8% in normal subjects whilst it was 10.6% to 24% in patients
with liver diseases. Above the age of 50 years, the prevalence rate increased
significantly, being 6.1% to 14.3% in normal subjects and 40.8% to 42.6% in
liver disease patients.
In both groups of subjects, the HCV marker positive cases gave a
previous history of blood transfusion and/or surgical operations at a higher
rate than HCV marker negative cases. In healthy subjects, amongst the
anti-HCV positive cases, 44.4% gave a previous history of blood transfusion
and surgical operation, whereas the rate was 20.1% in anti-HCV negative
cases. In patients with liver diseases, it was 88.4% in anti-HCV positive
cases and 39.1% respectively in anti-HCV negative cases.
Discussion
HCV poses a serious worldwide health problem and an estimated
100 million individuals globally are chronically infected with it. The
prevalence rate differs from country to country. In the present study, the
detection of anti-HCV in apparently healthy subjects without liver disease
was approximately 2.5%. This figure was higher than those reported from
Western Europe, Japan, USA, Bangladesh or Indonesia and was comparable to
that of Northern Italy and much less than in blood donors of Egypt.
In this study, the prevalence of HCV marker in the patients with
liver disease was approximately ten times higher than those in the healthy
subjects (25% to 2.5%). This higher prevalence was expected, as HCV infection
was reported to be associated with a wide spectrum of liver diseases ranging
from asymptomatic carriage to severe forms of chronic hepatitis, the major
complication being development of cirrhosis and HCC. In Singapore, the positivity rate for anti-HCV was 1.7% in normal healthy population, 3% in chronic hepatitis B carriers and 20% in primary HCC cases.9
Our study also showed that the prevalence of anti-HCV became significantly
higher in the more serious liver ailments, as it was not detected in fatty
liver, 10% positivity in acute hepatitis cases,
17.2% in chronic hepatitis cases and 38.5% and 29.3% in cirrhosis and HCC
cases respectively. A previous study in Myanmar showed that in HCC cases, 35% were positive for anti-HCV.5
A retrospective study on the serum of hepatitis B carriers in Myanmar, stored frozen in
1994, showed that 2.2% were positive for anti-HCV using HCV serum cassette
tests, Fresno, USA.12
Esteban and group in 1991 reported that in their study among
blood donors in Spain, there was no
difference in prevalence with respect to sex (1.17% males, 1.08% females).
However, the seroprevalence among male donors under
30 was three times higher than that among female donors in the same age group (1% vs 0.3%).13
Studies of HCV infection in the United States showed that males predominate slightly over females.14,15 In the present study, Myanmar females showed a
higher incidence in both the apparently normal group of subjects (4.9% to 0%)
and patients with liver disease (29.9% to 22.3%).
The incidence of HCV infection was reported to vary by age. The
analysis of the HCV carrier state in over 100 million Japanese blood donors showed
no anti-HCV positivity in subjects between 6-15
years, 0.36% positivity in subjects between 16 to 20 years, gradually increasing to about 2.8% in those older than 50 years.11
In USA, HCV seroprevalence among blood donors ranges from 0.5 per
1 000 in donors younger than 20 years, to 6.9 per 1 000 in donors of ages 30 to 39 years.16
Our study also showed that in control subjects as well as in patients with
liver disease, there was no anti-HCV positivity
below 20 years of age. From then on, the anti-HCV positivity
increased gradually from 1.1% in healthy subjects and 11.6% in patients
between 21 to 30 years group up to 14.3% and 42.6% respectively in those
above 60 years of age.
The study in Spain also showed that a
history of blood transfusion, intravenous drug abuse and tattooing was
significantly more common among anti-HCV positive donors than in seronegative controls.13
This was in accordance with the findings in the present study, where a higher
number of anti-HCV positive cases had a history of blood transfusion and
surgical operations than in seronegative subjects.
It was also reported from a study in USA that among
recipients of blood transfusion and control subjects of untransfused
hospital patients having similar diagnosis and undergoing generally similar
operative procedures, 3.3% of the blood recipients and only 0.1% of the control subjects seroconverted to anti-HCV.17
This study showed that HCV infection is highly prevalent in Myanmar both in the
apparently healthy population as well as in patients with end stage liver
diseases such as cirrhosis and HCC. Since no vaccine is as yet available for
HCV infection, the most effective control measure would be to prevent this
potentially life-threatening viral disease. Preventive measures include the
screening and testing of blood, plasma, organ, tissue and serum donors, virus
inactivation of plasma-derived products, risk-reduction counselling
and services, implementation and maintenance of infection control practices,
identification, counselling and testing of persons
at risk, medical management of infected persons, health education, surveillance and research.18
Since this is a preliminary report from a study in a limited group of
subjects, further large scale surveys will be required to determine the
prevalence of HCV infection throughout Myanmar.
Acknowledgement
This study was supported by a grant from the World Health
Organization.
References
1. Fortuny, C, Ercilla, M G, Barrera,
JM, Gil, C et al (1991) Vertical Transmission of hepatitis C virus (HCV): A
prospective study in infants born to HCV-seropositive
mothers. In: Viral Hepatitis and Liver Diseases. Proceedings of the 1990
International Symposium on Viral Hepatitis and Liver Disease: Contemporary
Issues and Future Prospects. Editors: F B Hollinger, S M Lemon and H Margolis
Williams and Wilkins, USA
pp 418-419. 2. Ng, HS (1995) Acute Hepatitis. In
Management of Common Gastroentero-logical Problems.
Editors: Guan, R, Kang, JY, Ng, HS Medimedia Asia Pte Ltd. pp 123-136. 3. Sherlock, S, Dusheiko,
G (1991) Hepatitis C virus updated. Gut, 32, 965-967. 4. Coppola, R, Rizzetto,
M, Bradley, D W(1996) Hepatitis C. In: Viral
Hepatitis Handbook. Editor: O Crivelli. Sorin Biomedica Diagnostics.
SPA Italy. pp
57-84. 5. Khin Pyone Kyi,
Khin Maung Win, Myo Aye, Yee Yee Htwe, Khin May Oo, Than Aung, San San Oo. Prevalence of hepatitis
B and C infections in hepatocellular carcinoma
cases in Myanmar.
Myanmar
Health Sciences Research Journal 1998 Vol. 10, No. 1, pp 1-5. 6. Bellentani, S, Tiribelli, C, Saccoccio, G, Soddie, M, Fratti, N, De Martin, C, Cristiani,
G (1994) Prevalence of chronic liver diseases in the general population of
Northern Italy. Hepatology 1994: 20: 1442-9. 7. Khan, Mobin,
Ahmad, N (1998) Sero-epidemiology of HBV and HCV in
Bangladesh.
EPI Research Information, Vol.1, No.6, July/August 1998: EPI Division, WHO.
SEARO, Delhi, pp1. 8. Suwignyo, S (1998) Sero-epidemiology
of HBV and HCV in Indonesia.
EPI Research Information, Vol.1, No.6, July/ August 1998: EPI Division, WHO.
SEARO, Delhi, pp1. 9. Khin, LW, Teo, CJ, Guan, R (1996) Seroprevalence of hepatitis B and C viral markers in
patients with primary hepatocellular carcinoma in
Singapore. Singapore
Medical Journal 1996; Vol. 37: 492-496. 10.
Apichartpiyakul, C, Apichartpiyakul,
N, Urwijitaroon, Y, Gray, J, Natpratan,
C, Katayama, Y, Fujii, M and Hotta,
H (1999) Seroprevalence and subtype distribution of
hepatitis C virus among blood donors and intravenous drug users in Northern/
North Eastern Thailand. Japanese Journal of Infectious Diseases 52, 121-123. 11.
Houghton, Michael (1996) Hepatitis C
Viruses. In: Fields Virology, Third Edition. Editors: B N Fields, D M Knipe, P M Howley. Lippincott- Raven Publishers, Philadelphia.
pp 1035-1053.
12. Khin Pyone Kyi
(1998) Hepatitis C:Situation
Report in Myanmar. Report from the Vaccine Production and Distribution Division, Department
of Medical Research, Yangon, Myanmar
(unpublished data) 13.
Esteban, R, Esteban, JI, Lopez-Talavera, J C, Genesca, J, Buti, M, Vargas, V and Guardia, J (1991) Epidemiology of
hepatitis C virus infection. In: Viral Hepatitis and Liver Diseases.
Proceedings of the 1990 International Symposium on Viral Hepatitis and Liver
Disease: Contemporary Issues and Future Prospects. Editors: FB Hollinger, SM
Lemon and H Margolis Williams and Wilkins, USA.
pp 413-415. 14.
Alter, MJ, Hadler,
S C, Judson, FN, et al. Risk factors for acute Non-A, Non-B hepatitis in the
US and association with HCV infection. Journal of American Medical
Association, 1990, 264: 2231-35. 15.
Mc Quillan, G M,
Alter, MJ, Moyer, LA, Lambert, SB, Margolis, HSA population based serologic
study of HCV infection in the US. In Rizzetto, M,
Purcell, RH, Gerin, JL, Verme,
G Editors. Viral Hepatitis and Liver Diseases, Edizioni
Minerva Medica, Turin,
1997, 267-270. 16.
Urdea, MS,
Wuestehube, LJ, Laurenson,
PM, Wilber, JC (1997) Clinical Chemistry 43:8 (B) 1507-1511. 17.
Mosley, JW, Stevens, CE, Aach, RD, Hollinger, FB and Barbosa,
L H (1991) Role of hepatitis C virus infection in transfusion associated
Non-A, Non-B hepatitis. In: Viral Hepatitis and Liver Diseases. Proceedings
of the 1990 International Symposium on Viral Hepatitis and Liver Disease:
Contemporary Issues and Future Prospects. Editors: FB Hollinger, SM Lemon and
H Margolis. Williams and Wilkins, USA.
pp 402 - 407. 18.
Centres for Disease Control and Prevention.
Recommendations for prevention and control of hepatitis C virus (HCV)
infection and HCV-related chronic disease. Morbidity and Mortality Weekly
Report (MMWR) 1998; 47 (No. RR-19) pp1-16. *
Department of Medical Research (Lower Myanmar), No. 5, Ziwaka
Road, Dagon PO, 11191, Yangon, Union of Myanmar. ** Liver Unit, YangonGeneralHospital, Department of Health
|