Evaluation of variants in IL6R, TLR3, and DC-SIGN genes associated with dengue in a sampled Colombian population

Introduction: Host genetics is recognized as an influential factor for the development of dengue disease. Objective: This study evaluated the association of dengue with the polymorphisms rs8192284 for gene IL6R, rs3775290 for TLR3, and rs7248637 for DC-SIGN. Materials and methods: Of the 292 surveye...

Full description

Autores:
Avendaño Tamayo, Efrén De Jesús
Rúa Cardona, Alex Fernando
Parra Marín, María Victoria
Rojas Montoya, Winston
Campo Nieto, Omer
Chacón Duque, Juan Camilo
Agudelo Flórez, Piedad Matilde
Narváez Rojas, Carlos Fernando
Salgado García, Doris Martha Cecilia
Restrepo Jaramillo, Berta Nelly
Bedoya Berrío, Gabriel de Jesús
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Tecnológico de Antioquia
Repositorio:
Repositorio Tdea
Idioma:
eng
OAI Identifier:
oai:dspace.tdea.edu.co:tdea/2798
Acceso en línea:
https://dspace.tdea.edu.co/handle/tdea/2798
Palabra clave:
Polymorphism
Polimorfismo
Polimorfism genetic
Genetic polymorphism
Polimorfismo genético
Toll-Like Receptor 3
Receptor Toll-Like 3
Receptor 3 Toll-Like
Colombia
Colômbia
Dengue/genetics
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
Description
Summary:Introduction: Host genetics is recognized as an influential factor for the development of dengue disease. Objective: This study evaluated the association of dengue with the polymorphisms rs8192284 for gene IL6R, rs3775290 for TLR3, and rs7248637 for DC-SIGN. Materials and methods: Of the 292 surveyed subjects, 191 were confirmed for dengue fever and the remaining 101 were included as controls. The genotypes were resolved using polymerase chain reaction and restriction fragment length polymorphism (PCRRFLP). In an attempt to determine the risk (Odds Ratio) of suffering dengue fever, data were analyzed using chi-square for alleles and logistic regression for both genotypes and allelic combinations. Confidence intervals were set to 95% for all tests regardless of the adjustment by either self-identification or ancestry