Dissection of familial correlations in Hepatitis C Virus (HCV) seroprevalence suggests evidence for intrafamilial viral transmission and genetic predisposition to infection

Sabine Plancoulaine ^1*, Mostafa Kamal Mohamed ², Naglaa Arafa ², Iman Bakr ², Claire Rekacewicz ³, David-Alexandre Trégouët ⁴, Dorothée Obach ³, Mai El Daly ⁵, Valérie Thiers ³, Cyrille Féray ⁶, Mohamed Abdel-Hamid ⁷, Laurent Abel ¹ and Arnaud Fontanet ³

¹ INSERM U550, France
² Ain Shams University, Egypt
³ Institut Pasteur, France
⁴ INSERM U525, France
⁵ National Liver Institute, Egypt
⁶ INSERM CIC04, France
⁷ National Hepatology and Tropical Medicine Research Institute, Egypt

^* To whom correspondence should be addressed. E-mail: plancoulaine{at}necker.fr.

Accepted 29 April 2008

Abstract

Objective: Unsafe therapeutic injections and transfusions are held responsible for many cases of Hepatitis C virus (HCV) transmission in developing countries, but cannot account for a substantial proportion of present infections. The aim of the present work was to investigate familial clustering of HCV infection in a population living in a highly endemic area.

Design, setting and participants: A large seroepidemiological survey was conducted on 3994 subjects (age range 2-88 years) from 475 familial clusters in an Egyptian rural area. Epidemiological methods appropriate for the analysis of correlated data were used to estimate risk factors and familial dependences for HCV infection. A phylogenetic analysis was conducted to investigate HCV strain similarities within and among families.

Main outcome measures: HCV familial correlations adjusted for known risk factors, similarities between viral strains.

Results: Overall HCV seroprevalence was 12.3%, increasing with age. After adjustment for relevant risk factors, highly significant intrafamilial resemblances in HCV seroprevalence were obtained between father-offspring (odds ratio =3.4[95%CI 1.8-6.2]), mother-offspring (3.8[2.5-5.8]), and sib-sib (9.3[4.9-17.6]), while a weaker dependence between spouses (2.2[1.3-3.7]) was observed. Phylogenetic analysis showed greater HCV strain similarity between family members than between unrelated subjects indicating that correlations can be explained in part by familial sources of virus transmission. In addition, refined dissection of correlations between first-degree relatives supported the role of host genes predisposing to HCV infection.

Conclusions: Current HCV infection in endemic countries has a strong familial component explained, at least partly, by specific modes of intrafamilial viral transmission and by genetic predisposition to infection.