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Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.
- Duggal, Priya;
- Thio, Chloe L;
- Wojcik, Genevieve L;
- Goedert, James J;
- Mangia, Alessandra;
- Latanich, Rachel;
- Kim, Arthur Y;
- Lauer, Georg M;
- Chung, Raymond T;
- Peters, Marion G;
- Kirk, Gregory D;
- Mehta, Shruti H;
- Cox, Andrea L;
- Khakoo, Salim I;
- Alric, Laurent;
- Cramp, Matthew E;
- Donfield, Sharyne M;
- Edlin, Brian R;
- Tobler, Leslie H;
- Busch, Michael P;
- Alexander, Graeme;
- Rosen, Hugo R;
- Gao, Xiaojiang;
- Abdel-Hamid, Mohamed;
- Apps, Richard;
- Carrington, Mary;
- Thomas, David L
- et al.
Published Web Location
https://doi.org/10.7326/0003-4819-158-4-201302190-00003Abstract
Unlabelled
Chinese translationBackground
Hepatitis C virus (HCV) infections occur worldwide and either spontaneously resolve or persist and markedly increase the person's lifetime risk for cirrhosis and hepatocellular carcinoma. Although HCV persistence occurs more often in persons of African ancestry and persons with genetic variants near interleukin-28B (IL-28B), the genetic basis is not well-understood.Objective
To evaluate the host genetic basis for spontaneous resolution of HCV infection.Design
2-stage, genome-wide association study.Setting
13 international multicenter study sites.Patients
919 persons with serum HCV antibodies but no HCV RNA (spontaneous resolution) and 1482 persons with serum HCV antibodies and HCV RNA (persistence).Measurements
Frequencies of 792 721 single nucleotide polymorphisms (SNPs).Results
Differences in allele frequencies between persons with spontaneous resolution and persistence were identified on chromosomes 19q13.13 and 6p21.32. On chromosome 19, allele frequency differences localized near IL-28B and included rs12979860 (overall per-allele OR, 0.45; P = 2.17 × 10-30) and 10 additional SNPs spanning 55 000 base pairs. On chromosome 6, allele frequency differences localized near genes for HLA class II and included rs4273729 (overall per-allele OR, 0.59; P = 1.71 × 10-16) near DQB1*03:01 and an additional 116 SNPs spanning 1 090 000 base pairs. The associations in chromosomes 19 and 6 were independent and additive and explain an estimated 14.9% (95% CI, 8.5% to 22.6%) and 15.8% (CI, 4.4% to 31.0%) of the variation in HCV resolution in persons of European and African ancestry, respectively. Replication of the chromosome 6 SNP, rs4272729, in an additional 745 persons confirmed the findings (P = 0.015).Limitation
Epigenetic effects were not studied.Conclusion
IL-28B and HLA class II are independently associated with spontaneous resolution of HCV infection, and SNPs marking IL-28B and DQB1*03:01 may explain approximately 15% of spontaneous resolution of HCV infection.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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