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World J Gastroenterol. Nov 28, 2013; 19(44): 7880-7888
Published online Nov 28, 2013. doi: 10.3748/wjg.v19.i44.7880
Burden of pediatric hepatitis C
Mortada Hassan El-Shabrawi, Naglaa Mohamed Kamal
Mortada Hassan El-Shabrawi, Naglaa Mohamed Kamal, Pediatrics and Pediatric Hepatology, Faculty of Medicine, Cairo University, Giza 12411, Egypt
Author contributions: El-Shabrawi MH suggested the idea of the work; both authors shared in manuscript preparation, had made an important scientific contribution to the paper and had assisted with the drafting and revising of the manuscript, in accordance with the definition of an author as stated by the International Committee of Medical Journal Editors.
Correspondence to: Mortada Hassan El-Shabrawi, MD, Professor of Pediatrics and Pediatric Hepatology, Faculty of Medicine, Cairo University, 3 Nablos Street, Off Shehab Street, Mohandesseen, Giza 12411, Egypt. melshabrawi@medicine.cu.edu.eg
Telephone: +20-1-223133705 Fax: +20-2-37619012
Received: August 20, 2013
Revised: October 19, 2013
Accepted: November 2, 2013
Published online: November 28, 2013
Abstract

Hepatitis C virus (HCV) is a major health burden infecting 170-210 million people worldwide. Additional 3-4 millions are newly-infected annually. Prevalence of pediatric infection varies from 0.05%-0.36% in the United States and Europe; up to 1.8%-5.8% in some developing countries. The highest prevalence occurs in Egypt, sub-Saharan Africa, Amazon basin and Mongolia. HCV has been present in some populations for several centuries, notably genotypes 1 and 2 in West Africa. Parenteral anti-schistosomal therapy practiced in the 1960s until the early 1980s had spread HCV infection throughout Egypt. Parenteral acquisition of HCV remains a major route for infection among Egyptian children. Insufficient screening of transfusions, unsterilized injection equipment and re-used needles and syringes continue to be major routes of HCV transmission in developing countries, whereas vertical transmission and adolescent high-risk behaviors (e.g., injection drug abuse) are the major routes in developed countries. The risk of vertical transmission from an infected mother to her unborn/newborn infant is approximately 5%. Early stages of HCV infection in children do not lead to marked impairment in the quality of life nor to cognitive, behavioral or emotional dysfunction; however, caregiver stress and family system strain may occur. HCV slowly progresses to serious complications as cirrhosis (1%-2%) and hepatocellular carcinoma (HCC) especially in the presence of risk factors as hemolytic anemias, obesity, treated malignancy, and concomitant human immune deficiency and/or hepatitis B virus co-infection. HCV vaccine remains elusive to date. Understanding the immune mechanisms in patients who successfully cleared the infection is essential for vaccine development. The pediatric standard of care treatment consists of pegylated interferon-α 2a or b plus ribavirin for 24-48 wk. The new oral direct acting antivirals, approved for adults, need further evaluation in children. Sustained virologic response varies depending on the viral load, genotype, duration of infection, degree of aminotransferase elevation, adiposity and single nucleotide polymorphisms of interleukin (IL)-28B locus. The goals of treatment in individual patients are virus eradication, prevention of cirrhosis and HCC, and removing stigmatization; meanwhile the overall goal is decreasing the global burden of HCV. IL-28B polymorphisms have been also associated with spontaneous clearance of vertically acquired HCV infection. The worldwide economic burden of HCV for children, families and countries is estimated to be hundreds of millions of US dollars per year. The United States, alone, is estimated to spend 199-336 million dollars in screening, monitoring and treatment during one decade. The emotional burden of having an HCV infected child in a family is more difficult to estimate.

Keywords: Hepatitis C virus, Burden, Genotypes, Cost, Pediatrics

Core tip: Hepatitis C virus (HCV) is a worldwide health burden infecting up to 5.8% of children in some developing countries with thousands of annual new infections. HCV vaccine is illusive, but understanding immune mechanisms in patients who cleared infection may be crucial. The pediatric standard of care treatment is pegylated interferon-α2 plus ribavirin for 24-48 wk. The new oral direct acting antivirals need further evaluation in children. Interleukin-28B polymorphisms have been associated with treatment response and spontaneous clearance of vertical HCV infection. The worldwide economic burden of HCV is estimated to be hundreds of millions United States dollars/year. The emotional burden is difficult to estimate.