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Childhood Acquired Hepatitis C Virus Increases Risk Of Liver Disease

by Julia Samuel on Apr 24 2017 3:25 PM

Childhood Acquired Hepatitis C Virus Increases Risk Of Liver Disease
One-third of young people (<18 years old) with childhood acquired Hepatitis C Virus (HCV) develop serious long-term liver disease, 5% develop liver cancer and more than 4% undergo a liver transplant.
The cohort study, presented at The //International Liver Congress 2017 in Amsterdam, The Netherlands, revealed intravenous drug abuse as the main route of HCV infection in young people in the UK (53%, n=535/1,014).

Hepatitis C Virus

  • HCV is one of the most widespread transmissible diseases globally. It is estimated to infect over 185 million people worldwide, of whom 350,000 die each year, with 84,000 of those being in Europe.
  • HCV is considered a silent pandemic as most people do not know that they have it.1 HCV causes both acute and chronic infection, with about 55-85% of HCV-infected individuals developing chronic infection.
  • HCV is a leading cause of chronic liver disease, end-stage cirrhosis and liver cancer. In the United States, 23,000 to 46,000 children are estimated as having chronic HCV infection.
  • In developed countries, transmission of HCV in children is mainly through the mother at birth (perinatal transmission). HCV increases the risk of liver-related death by 26 times when acquired during childhood.
"Our study showed that more than one-third of young people infected with HCV in childhood have serious long-term liver disease," said Dr Line Modin, Birmingham Children's Hospital, United Kingdom, and first author of the study. "Detection of HCV should be aimed at relevant risk groups, particularly young intravenous drug abusers."

Data on patients with an estimated age at first HCV infection between 0 and 18 years old were analysed from a national clinical database (HCV Research UK) that covered 51 adult and seven paediatric centres. Data were collected between July 2012 and October 2016. The study included 1,014 patients, 731 (72%) of whom were males.

The most prevalent route for infection with HCV was intravenous drug abuse (535 individuals). Other means of infection included blood products (244 people) and acquiring HCV around the time of birth (116). Other risk factors accounted for HCV infection in 119 individuals.

The most common HCV genotype in the study was genotype 1 (57%). Over one-third (35%) had genotype 3, which is the most difficult subgroup of patients to cure and for which treatment options remain suboptimal.

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Liver disease was found in 354 patients (33%), with cirrhosis in 269 (27%), liver cancer (hepatocellular carcinoma) in 55 (5%) and 47 (5%) had undergone a liver transplant. Patients with perinatal exposure to HCV developed cirrhosis at an earlier age than the intravenous drug group (median of 36 years versus 48 years).

"Our study highlights how important it is that clinical trials of antiviral therapy are performed in children, to develop clear treatment guidelines to prevent long-term liver disease," said Professor Deirdre Kelly, Birmingham Children's Hospital, United Kingdom, and study lead.

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"This study from the UK suggests that many children infected perinatally may develop cirrhosis at a young age, if left untreated. Safe and efficacious direct-acting antiviral treatment should be made available to children, to prevent liver disease progression and viral spread at a later age," said Prof Francesco Negro, Divisions of Gastroenterology and Hepatology of Clinical Pathology, University Hospital of Geneva, Switzerland and EASL Governing Board Member.

Source-Eurekalert


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