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Hepatitis C may increase deaths from both liver-related and other diseases
JULY 18, 2012 - In a long-term study of people infected with the hepatitis C virus (HCV), researchers found increased
deaths from both liver-related and non-liver related diseases in patients with active infections who had not cleared their infection.
The study, published in the Journal of Infectious Diseases and available online, found increased mortality in patients with
chronic HCV infection-that is, with detectable levels of HCV genetic material, or RNA, in their blood-suggesting that chronic HCV
infections, even in people who have no symptoms, can lead to increased mortality from liver disease or a variety of other causes.
The findings highlight the importance of people getting tested for HCV antibodies and for active HCV infection-and of
evaluating patients for antiviral treatment when they are found to have an active HCV infection, even when they feel well.
HCV infects more than 170 million people globally and has been shown to cause such liver diseases as cirrhosis and
hepatocellular carcinoma. Many infected patients have no symptoms and are not aware of infection until after irreversible liver
disease has occurred. In addition, several diseases not related to the liver have been linked to HCV. However, nearly
two-thirds of patients can be cured of their HCV infection with currently available antiviral therapy.
Chien-Jen Chen, ScD, and researchers from the Genomic Research Center in Taipei, Taiwan, enrolled more than 23,000 adults
in Taiwan in their study and followed them from 1991 to 2008. Blood samples were collected at study entry and at follow-up health
examinations. Researchers found increased mortality from liver- and non-liver-related diseases-including cancers of the
esophagus, prostate, and thyroid, as well as circulatory and renal diseases-among those infected with HCV. Mortality
was higher in HCV-infected participants with detectable serum levels of HCV RNA, indicating they had active
infections; subjects with previous infections who only had HCV antibodies, but not HCV RNA, in their blood
did not have increased mortality on follow-up.
According to Dr. Chen, "The findings implied that the serum HCV RNA level is an important marker for clinical decisions in
the management of HCV-infected patients." Dr. Chen suggested that HCV-infected patients may benefit from treatment with antiviral and
immunomodulating agents to promote viral clearance.
The investigators concluded that their findings have significant implications for clinical practice and public health-namely,
that individuals seropositive for HCV RNA should be followed intensively and urged to be evaluated for antiviral therapy. In addition,
they noted, testing to determine serum HCV RNA level by a sensitive assay is essential for clinical management of HCV-infected patients.
Dr. Chen and his colleagues cautioned that some non-liver-related diseases are too rare to accurately determine their risk
in connection with HCV infection. They suggested that a collaborative study with a large sample size would be needed in order to further
investigate the full spectrum of diseases associated with HCV.
In an accompanying editorial, Kenrad E. Nelson, MD, of Johns Hopkins University in Baltimore, noted that overall mortality
was significantly increased from liver-related and other causes compared to uninfected patients from the same communities in the study.
The findings indicate that, although some who are infected with HCV can cure their infection without treatment, most people who are
infected and who have no symptoms develop chronic infections and are at increased risk of death from HCV, Dr. Nelson said.
Many patients with HCV infection go undiagnosed, and among those whose infection is detected, "few are medically
evaluated and effectively treated," Dr. Nelson added. Although treatment for HCV infection is improving dramatically, he noted,
a significant reduction in HCV-related mortality will require that screening measures are greatly expanded.
Fast Facts:
- Overall mortality in patients infected with hepatitis C virus (HCV) was significantly increased from both liver-related and other diseases compared to uninfected patients from the same communities.
- Compared to people who had never been infected with HCV, mortality was higher in HCV-infected patients with detectable levels of HCV RNA in their blood on follow-up, but not in patients with inactive infections-those who were positive for HCV antibodies but whose blood was free of HCV RNA.
- Diseases not related to the liver that were observed in this study included cancers of the esophagus, prostate, and thyroid, and circulatory and renal diseases.
- Most people with chronic HCV infection don't know they are infected because the infection is often without symptoms. However, chronic HCV can be curable with treatment, so people should be screened and considered for treatment if they have chronic HCV infection.
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Editor's note: This study was supported by research grants from the Taiwan Department of Health; Bristol-Myers Squibb Co.;
Academia Sinica in Taipei, Taiwan; and the National Health Research Institutes in Chunan, Taiwan.
The study and the accompanying editorial are available online. They are embargoed until 12:01 a.m. EDT on Wednesday,
July 18, 2012:
Founded in 1904, The Journal of Infectious Diseases is the premier publication in the Western Hemisphere
for original research on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and
on disorders of host immune mechanisms. Articles in JID include research results from microbiology, immunology, epidemiology,
and related disciplines. It is published under the auspices of the Infectious Diseases Society of America (IDSA). Based
in Arlington, Va., IDSA is a professional society representing nearly 10,000 physicians and scientists who specialize
in infectious diseases. For more information, visit www.idsociety.org .
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Source: EurekAlert!
http://www.eurekalert.org/pub_releases/2012-07/idso-hcm071712.php
Contact:
Sky Opila
sopila@pcipr.com
312-558-1770
Infectious Diseases Society of America
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