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Association between MTTP genotype (-493G/T) polymorphism and hepatic steatosis in hepatitis C: a systematic review
Xiaoxia Wang1, Yu Cao2, Jia Guo1
1Department of Medical Oncology, Beijing YouAn Hospital, Capital Medical University, Beijing, China.
Background:
Hepatitis C has been associated with the development of hepatic steatosis, which increases the risk of liver cancer. The microsomal triglyceride transporter protein (MTTP), is a lipid transport protein that mediates lipid metabolism and CD1d antigen presentation. The study aimed to explore the association between MTTP genotype (-493G/T) polymorphism and hepatic steatosis in hepatitis C.
Methods:
The database "Pubmed, Cochrane library, CNKI, Web of science, Embase and CBM" were retrieved to identify the literature. The quality of the selected literature was evaluated using the "the Newcastle-Ottawa Scale" (NOS). Relevant data was extracted and analyzed using the Stata software. Heterogeneity was expressed by "Cochran's Q and I2", with I2 ≥ 50% or P < 0.05 indicating high heterogeneity. A random-effects model and subgroup analysis were conducted to identify the sources of heterogeneity. We also used "Funnel plots", "Egger's tests" and "Begg's tests" to evaluate biases in the literature.
Results:
The study found a significant and positive association between liver steatosis and the HCV genotype 3 with a dominant model of the MTTP genotype (-493G/T) (OR = 11.57, 95%CI: 4.467-29.962, P < 0.001). In contrast, no correlation was found between hepatic steatosis and either the recessive, homozygous or heterozygous models (OR = 1.142, P = 0.5; OR = 1.581, P = 0.081; OR = 1.029, P = 0.86). There was no significant publication biases, as measured by the Funnel plot, and the Egger's and Begg's tests. Finally, sensitivity analysis showed the obtained results are stable.
Conclusions:
Dominant mutations in the T allele of the MTTP genotype (-493G/T) increase susceptibility to hepatic steatosis in patients presenting with the HCV genotype 3.
Insights
Microsomal triglyceride transporter protein (MTTP) genotype -493G/T polymorphism is associated with hepatic steatosis in Hepatitis C virus genotype 3 patients. Dominant mutations in the T allele increase susceptibility to fatty liver disease.
Area of Science:
- Hepatology
- Genetics
- Molecular Biology
Background:
- Hepatitis C virus (HCV) infection is linked to hepatic steatosis, a condition increasing liver cancer risk.
- Microsomal triglyceride transporter protein (MTTP) plays a role in lipid metabolism and CD1d antigen presentation.
- Investigating the association between MTTP genotype (-493G/T) polymorphism and hepatic steatosis in HCV patients is crucial.
Approach:
- A comprehensive literature search was conducted across multiple databases (PubMed, Cochrane, CNKI, Web of Science, Embase, CBM).
- Study quality was assessed using the Newcastle-Ottawa Scale (NOS), and data were analyzed using Stata.
- Heterogeneity, publication bias, and sensitivity were evaluated using established statistical methods (Cochran's Q, I², Egger's, Begg's tests, Funnel plots).
Key Points:
- A significant positive association was found between hepatic steatosis and HCV genotype 3 under a dominant model of the MTTP genotype (-493G/T) (OR = 11.57, P < 0.001).
- No significant correlation was observed for recessive, homozygous, or heterozygous models.
- Sensitivity analysis confirmed the stability of the findings, with no significant publication biases detected.
Conclusions:
- Dominant mutations in the T allele of the MTTP genotype (-493G/T) are associated with increased susceptibility to hepatic steatosis.
- This association is particularly evident in patients with Hepatitis C virus genotype 3.
- The findings highlight a potential genetic marker for fatty liver disease in specific HCV populations.
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