Last Updated: 2002-07-17 17:00:48 -0400
(Reuters Health)
NEW YORK (Reuters Health) - Testing for the presence of two
proteins associated with hepatitis B may indicate whether or not patients
with the liver-infecting virus will go on to develop cancer, new study
findings suggest.
While many people recover within a few months of a hepatitis B virus
(HBV) infection, some can develop chronic infection, which can lead to
cirrhosis (scarring), liver cancer, liver failure and death. Hepatitis B
vaccine is available for all age groups to prevent HBV infection.
Little is known about how frequently people are able to clear infection
on their own and how frequently those with chronic HBV infection go on to
develop liver cancer or liver failure.
In the current study, lead author Dr. Hwai-I Yang of the National Taiwan
University in Taipei and colleagues evaluated the liver cancer status of
11,893 men infected with HBV over a 10-year period.
All of the men were free of liver cancer at the start of the study in
1991, the authors note in their report published in the July 18th issue of
The New England Journal of Medicine.
At the study's end in 2000, a total of 111 cases of liver cancer were
reported. Yang's group found that men who tested positive for a protein
produced by the virus, called hepatitis B surface antigen (HBsAg), were
nearly 10 times more likely to develop liver cancer. In addition, men who
tested positive for HBsAg and another protein, called hepatitis B e antigen
(HBeAg), were 60 times more likely to develop liver cancer compared with men
who did not have either protein in their blood.
The authors estimate that for every 100,000 men infected with hepatitis
B, 39 men negative for HBeAG and HBsAg would develop liver cancer in a given
year, compared with 324 per 100,000 men with HBsAg only and 1,169 per
100,000 men with both proteins.
"HBeAg, in addition to HBsAg, may be a useful marker of the risk of
(liver cancer)," the researchers report.
"Persons considered to be at high risk because of positivity for HBeAg
would be candidates for antiviral-drug treatment and close monitoring for
the development of liver diseases associated with chronic HBV infection,"
Yang and colleagues conclude.
SOURCE: The New England Journal of Medicine
2002;347:168-174.
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