Journal
SCIENTIFIC REPORTS
Volume 7, Issue -, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41598-017-09548-9
Keywords
-
Categories
Funding
- China Postdoctoral Science Foundation [2015M570518]
- National ST Major Project [2016ZX10002020]
- Swedish Research Council (V.R.) [254439006]
- Swedish Heart Lung Foundation [244439007]
- Swedish federal government funding under the LUA/ALF agreement [76290]
- Novonordisk Foundation Grant for Excellence in Endocrinology [244439012]
- Swedish Diabetes Foundation [DIA 2014-052]
- Knut and Alice Wallenberg Foundation
- Ricerca Corrente, Fondazione IRCCS Ca' Granda Milano (Institutional research funds
- Public Research Institute)
- Fondazione Policlinico - INGM Molecular Medicine
- First AIRC Grant [16888]
Ask authors/readers for more resources
The impact of Transmembrane 6 superfamily member 2 (TM6SF2) E167K variant, which causes hepatocellular fat retention by altering lipoprotein secretion, on liver damage and metabolic traits in chronic hepatitis C patients is still debated. We performed a systematic review and meta-analysis to clarify this relationship. Four studies with a total of 4325 patients were included. The risk of histologically-determined advanced steatosis, fibrosis, and cirrhosis (but not of severe inflammation) were increased in carriers of the TM6SF2 variant (P < 0.05). Unlike the inconsistent association with steatosis severity, due to the confounding effect of infection by the genotype-3 hepatitis C virus, the TM6SF2 variant was robustly associated with advanced fibrosis (OR = 1.07; 95% confidence interval [CI] = 1.01-1.14) and in particular with cirrhosis (OR = 2.05; 95% CI = 1.39-3.02). Regarding metabolic features, individuals positive for the TM6SF2 variant exhibited 5.8-12.0% lower levels of circulating triglycerides and non-HDL cholesterol (P < 0.05). Carriers of the variant were leaner, but there was high heterogeneity across studies (I-2 = 97.2%). No significant association was observed between the TM6SF2 variant and insulin resistance or hepatitis C viral load (both P > 0.05). In conclusion, the TM6SF2 E167K variant promotes the development of steatosis, fibrosis and cirrhosis in patients with chronic hepatitis C. Conversely, this variant reduces circulating atherogenic lipid fractions.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available