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Effect of MTTP -493G/T, I128T, Q95H and Q244E polymorphisms on hepatic steatosis in patients with chronic hepatitis
Prata, Thamiris Vaz Gago; Manchiero, Caroline; Dantas, Bianca Peixoto; Nunes, Arielle Karen da Silva; Tengan, Fátima Mitiko; Magri, Mariana Cavalheiro.
  • Prata, Thamiris Vaz Gago; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
  • Manchiero, Caroline; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
  • Dantas, Bianca Peixoto; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
  • Nunes, Arielle Karen da Silva; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
  • Tengan, Fátima Mitiko; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
  • Magri, Mariana Cavalheiro; Universidade de São Paulo (HCFMUSP). Faculdade de Medicina. Hospital das Clínicas. São Paulo. BR
Clinics ; 77: 100094, 2022. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1404290
ABSTRACT
Abstract

Background:

Chronic hepatitis C is characterized by a progressive deterioration of liver function and is involved in metabolic complications, such as hepatic steatosis.

Objective:

The aim of this study was to investigate the role of host and viral characteristics associated with -493G/T (rs1800591), I128T (rs3816873), Q95H (rs61733139), and Q244E (rs17599091) Single Nucleotide Polymorphisms (SNPs) in the Microsomal Triglyceride Transfer Protein (MTTP) gene on hepatic steatosis in chronic hepatitis C.

Methods:

SNPs were genotyped by PCR-RFLP and analyzed in combination with host and viral characteristics by multiple logistic regression in different genetic models of inheritance.

Results:

The authors analyzed 236 patients with chronic hepatitis C, and 53% had hepatic steatosis. The mutated allele frequencies were > 5%, and the genotypes were in Hardy-Weinberg equilibrium (p ≥ 0.05). It was observed that patients with HCV genotype 3 infection (OR = 2.74, 95% CI 1.24‒6.06, p = 0.013), female sex (OR = 2.28, 95% CI 1.21‒4.28, p = 0.011) and moderate- and high-intensity liver inflammatory activity (A2-A3) (OR = 3.61, 95% CI 1.86‒7.01, p < 0.001) alone exhibited a higher risk of steatosis. The results of multiple logistic regression analysis for interaction showed that for the -493G/T SNP, when the GT/TT genotype (dominant model) and the GT genotype (codominant model) were each combined with HCV genotype 3 infection, an 11.51-fold (95% CI 2.08‒63.59, p = 0.005) and a 15.69-fold (95% CI 2.46‒99.85, p = 0.004) increased risk of steatosis, respectively, was observed. For the I128T SNP, when both the IT/TT genotype (dominant model) and the IT genotype (codominant model) were combined with HCV genotype 3 infection, an 8.51-fold (95% CI 1.59‒45.54, p = 0.012) and an 8.40 fold (95% CI 1.51‒46.91, p = 0.015) increased risk of steatosis, respectively, was observed.

Conclusion:

The present study showed that the viral genotype combined with the -493G/T and I128T SNPs in the MTTP gene influences hepatic steatosis.


Full text: Available Index: LILACS (Americas) Type of study: Prognostic study Language: English Journal: Clinics Journal subject: Medicine Year: 2022 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo (HCFMUSP)/BR

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Full text: Available Index: LILACS (Americas) Type of study: Prognostic study Language: English Journal: Clinics Journal subject: Medicine Year: 2022 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo (HCFMUSP)/BR