Artikel Hepatitis B viral load, genotype affect liver cancer risk, study finds

Infection with a specific subtype of hepatitis B virus (HBV) and a high viral load are associated both independently and additively with an increased risk of a type of liver cancer, according to a new study in the February 16 issue of the Journal of the National Cancer Institute.
Chronic infection with HBV has been established as a cause of hepatocellular carcinoma (HCC), a type of liver cancer. More than 350 million people worldwide have a chronic infection with one of the seven known genotypes, or subtypes, of HBV. Although there are some known risk factors for HCC development, it is unclear what role HBV subtype or viral load--the amount of the virus in the blood--might have on cancer development.

To determine whether HBV genotype and viral load are associated with HCC risk, Ming-Whei Yu, Ph.D., of National Taiwan University in Taipei, and colleagues conducted a nested case–control study among male Taiwanese HBV carriers who had not been diagnosed with HCC. HBV DNA levels--a measure of viral load--and genotypes were determined for 154 case patients (men who were diagnosed with HCC during 14 years of follow-up) and 316 control subjects.

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Transmission of Hepatitis C among family members

The prevalence of antibodies to Hepatitis C Virus (HCV) in Egypt is among the highest in the world. From the 1950s until 1982 hundreds of thousands were infected during mass campaigns to control schistosomiasis (a parasitic disease) using mass therapy with intravenous antimony compounds, but little is known about current risk factors and rates of transmission. Studies of high risk populations, such as intravenous drug users, shed little light on HCV transmission in Egypt where this high risk behavior is rare.

In a study led by G. Thomas Strickland, M.D. of the Department of Epidemiology and Preventive Medicine at the University of Maryland School of Medicine in Baltimore, MD and published in the September 2005 issue of Hepatology, Egyptian and American researchers surveyed rates of HCV infection in two rural communities having a prevalence of antibody to HCV of 24 and 9 percent.

A total of 10,112 HCV negative individuals were identified during an annual survey in 1997, with follow-up performed on an average of 1.6 years later in 6,738 subjects. Of these, 33 developed HCV antibodies, an incidence of 3.1/1000 person-years (PY), and 6.8/1000 PY in the 28 subjects in the village having the 24 percent prevalence of HCV. None of the 33 individuals was diagnosed with viral hepatitis or reported symptoms of acute hepatitis. An analysis of risk factors showed the strongest predictor of infection with HCV was having and anti-HCV positive family member. Among those that did, incidence was 5.8/1000 PY, compared to 1.0/1000 PY; 27/33 incident cases had an anti-HCV positive family member. Parenteral exposures increased the risk of HCV, but were not statistically significant; 67 percent of seroconverters were less than 20 years old, and the highest incidence rate (14.1/1000 PY) was in children under 10 living in households with an anti-HCV positive parent in the village with the high prevalence of HCV antibodies. The infection rate was also increased (13.1/1000 PY) in men married to an HCV positive woman.

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Novel therapy combinations gain ground in treating hepatitis

LOS ANGELES (May 21, 2006) - According to recent estimates, hepatitis has become a worldwide health problem, affecting millions of people in the U.S. and abroad.
Researchers are experimenting with combinations of anti-inflammatory medicines like interferons to improve hepatitis symptoms. In research presented today at Digestive Disease Week® 2006 (DDW), new combinations of therapies are making significant progress to improve symptoms of the disease. DDW is the largest international gathering of physicians and researchers in the fields of gastroenterology, hepatology, endoscopy and gastrointestinal surgery.

Hepatitis is caused by a virus that attacks the liver, triggering painful inflammation and often leading to more serious conditions like liver failure and even death. Several different forms of hepatitis exist, including hepatitis A, B and C. Hepatitis A is generally food-borne, while hepatitis B and C are spread primarily through parenteral or sexual routes. The disease is often caused by a virus, but can also result from alcohol, toxins or drugs.

"Despite the significant number of people suffering from hepatitis, treatment options have been lagging in comparison to other major diseases," said John Vierling, M.D., FACP, president, the American Association for the Study of Liver Diseases (AASLD); professor of Medicine and Surgery at the Baylor College of Medicine in Houston, Texas; and director of Baylor Liver Health and Chief of Hepatology. "We hope that continued research like these studies will lead to more significant breakthroughs and relief for these patients."

Valopicitabine (NM283), Alone or with Peg-Interferon, Compared to Peg Interferon/Ribavirin (pegIFN/RBV) Retreatment in Hepatitis C Patients with Prior Non-Response to PegIFN/RBV: Week 24 Results [Abstract 4]

More than half of currently treated hepatitis patients are infected with strains of hepatitis C that do not respond to current interferon therapies and have no other effective treatment options. Combination treatment using a new antiviral therapy is showing promise in suppressing the virus, according to a phase II US multi-center study. The therapy, valopicitabine, has shown anti-HCV activity alone and in combination with pegIFN (pegylated interferon) in early trials, without viral breakthrough for study periods up to six months.

The current study compared the outcomes of five different treatments in patients who have not experienced remission with standard therapies: valopicitabine alone (800 mg/d), one of three combination arms with the drug at 400 mg/d, 800 mg/d or dose-ramping 400 to 800 mg/d plus pegIFN, or pegIFN with ribavirin as a control group.

For the 162 patients who have completed the trial period at 24 weeks, results show that the two higher-dose combination arms had much better response rates than the control group, experiencing on average a 2.5 to 3.0 log decrease in hepatitis RNA reductions by week 24, a significantly better response than the comparator. No viral breakthrough has been seen to date. However, vomiting and dehydration requiring hospitalization occurred in three patients taking the highest dose (800 mg), forcing the research team to halt the use of that dose and continue using only the lower doses of 200 to 400 mg of the drug.

"For patients whose disease has not responded to current therapies, this new combination treatment may produce excellent results, at the maximally acceptable dosage," according to Paul Pockros, M.D., of Scripps Clinic in California, and lead study author. "Continued treatment will determine if these encouraging early responses will result in a sustained response, hopefully improving patient quality of life and long-term survival."

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