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Molecular genetic association of rs8099917 and rs1800795 polymorphisms in the progression of hepatitis Delta virus liver disease
Passos-Silva, Ana Maísa; Silva, Eugênia de Castro e; Borzacov, Lourdes Maria Pinheiro; Araújo, Adrhyan; Porto, Anita Sperandio; Salcedo, Juan Miguel Villalobos; Vieira, Deusilene.
  • Passos-Silva, Ana Maísa; Oswaldo Cruz Foundation Rondonia. Molecular Virology Laboratory. Porto Velho. BR
  • Silva, Eugênia de Castro e; Tropical Medicine Research Center. Porto Velho. BR
  • Borzacov, Lourdes Maria Pinheiro; Tropical Medicine Research Center. Porto Velho. BR
  • Araújo, Adrhyan; Oswaldo Cruz Foundation Rondonia. Molecular Virology Laboratory. Porto Velho. BR
  • Porto, Anita Sperandio; Federal University of Rondonia. Porto Velho. BR
  • Salcedo, Juan Miguel Villalobos; Federal University of Rondonia. Porto Velho. BR
  • Vieira, Deusilene; Oswaldo Cruz Foundation Rondonia. Molecular Virology Laboratory. Porto Velho. BR
J. venom. anim. toxins incl. trop. dis ; 30: e20230025, 2024. tab, graf, ilus
Article Dans Anglais | LILACS, VETINDEX | ID: biblio-1528979
ABSTRACT

Background:

The relationship between viral infections and host factors holds high hopes for identifying the role of Interferon Lambda 3 (IFNL3) and Interleukin 6 (IL-6) polymorphisms in the development of Chronic Liver Disease (CLD) in patients infected with hepatitis Delta virus (HDV) in the Western Brazilian Amazon.

Methods:

Cross-sectional study conducted with a cohort of 40 chronic HDV patients, 27 with CLD and 13 without evident liver damage. Biological samples from the participants were analyzed using the polymerase chain reaction (PCR) technique, followed by sequencing by the automated Sanger method.

Results:

The rs8099917 T allele, from the IFNL3 gene, showed a higher frequency in both groups; however, it was not possible to establish an association with HDV infection [OR = 1.42 (0.42 - 4.75; p = 0.556 (95% CI). For IL-6, the rs1800795 G allele was superior to rs1800795 C. Analyzing both distributions in the studied groups, any association with HDV was absent (p > 0.05).

Conclusion:

The results suggest that the rs8099917 T/G (IFNL3) and rs1800795 G/C (IL-6) polymorphisms are not associated with the evolution of HDV in the studied population.
Sujets)


Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Virus de l'hépatite delta / Hépatite D chronique / Polymorphisme de nucléotide simple Type d'étude: Étude observationnelle / Étude pronostique / Facteurs de risque Limites du sujet: Humains Pays comme sujet: Amérique du Sud / Brésil langue: Anglais Texte intégral: J. venom. anim. toxins incl. trop. dis Thème du journal: Toxicologie Année: 2024 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Federal University of Rondonia/BR / Oswaldo Cruz Foundation Rondonia/BR / Tropical Medicine Research Center/BR

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Virus de l'hépatite delta / Hépatite D chronique / Polymorphisme de nucléotide simple Type d'étude: Étude observationnelle / Étude pronostique / Facteurs de risque Limites du sujet: Humains Pays comme sujet: Amérique du Sud / Brésil langue: Anglais Texte intégral: J. venom. anim. toxins incl. trop. dis Thème du journal: Toxicologie Année: 2024 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Federal University of Rondonia/BR / Oswaldo Cruz Foundation Rondonia/BR / Tropical Medicine Research Center/BR