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©2013 Baishideng Publishing Group Co.
World J Gastroenterol. Nov 7, 2013; 19(41): 7055-7061
Published online Nov 7, 2013. doi: 10.3748/wjg.v19.i41.7055
Published online Nov 7, 2013. doi: 10.3748/wjg.v19.i41.7055
Cohorts size | Study design | HCV genotype | IFNL3 SNP | % IR | HOMA-IR | Results | Ethnicity | Ref. |
434 | Multi-center, retrospective | HCV-1 (n = 434) | rs12979860 | 50% | > 3 | CC genotype associated with reduced IR | Caucasians | 48 |
202 | Prospective | HCV-1 (n = 181) | rs12979860 | 32.20% (65/202) | ≥ 3 | CC genotype associated with reduced IR | Caucasians | 49 |
HCV-4 (n = 21) | ||||||||
328 | Retrospective | HCV-1 (n = 328) | rs8099917 | 50% (84/168) in TT genotype vs 69.7% (53/76) in TG/GG genotype | ≥ 2.45 in TT genotype vs≥ 1.55 in TG/GG genotype | No differences in IFNL3 genotype distribution according to HOMA-IR | Japanese | 57 |
240 | Retrospective | HCV-1 (n = 188) | rs12979860 | 46% (89/193) | ≥ 2 | No differences in HOMA-IR levels according to IFNL3 genotypes | Caucasians | 59 |
HCV-2 (n = 3) | ||||||||
HCV- (n = 30) | ||||||||
HCV-4 (n = 19) |
- Citation: Eslam M, Booth DR, George J, Ahlenstiel G. Interaction of IFNL3 with insulin resistance, steatosis and lipid metabolism in chronic hepatitis C virus infection. World J Gastroenterol 2013; 19(41): 7055-7061
- URL: https://www.wjgnet.com/1007-9327/full/v19/i41/7055.htm
- DOI: https://dx.doi.org/10.3748/wjg.v19.i41.7055