Copy Number Variation and Frequency of rs179008 in TLR7 Gene Associated with Systemic Lupus Erythematosus in Two Mexican Populations

Author:

Pacheco Guillermo Valencia1ORCID,Nakazawa Ueji Yumi E.1ORCID,Bello Julián Ramírez2ORCID,Barbosa Cobos Rosa E.3ORCID,Jiménez Becerra Eduardo D.1,González Herrera Lizbeth J.4ORCID,Pérez Mendoza Gerardo J.1ORCID,Rivero Cárdenas Nubia A.1,Angulo Ramírez Angélica V.5ORCID,López Villanueva Ricardo F.6ORCID

Affiliation:

1. Hematology Laboratory, Regional Research Center, Autonomous University of Yucatán, Yucatán, Mexico

2. Endocrinology Department, National Institute of Cardiology Ignacio Chávez, México City, Mexico

3. Rheumatology Department, Hospital Juárez de México, México City, Mexico

4. Genetic Laboratory, Regional Research Center, Autonomous University of Yucatán, Yucatán, Mexico

5. Rheumatology Department, Hospital General Dr. Agustín O’Horán, Health Service Yucatán, Yucatán, Mexico

6. Rheumatology Department, Regional Hospital General (ISSSTE), Health Service Yucatán, Yucatán, Mexico

Abstract

Systemic Lupus Erythematosus (SLE) is an autoimmune disease in which genetic factors play a role in the susceptibility to develop it. Genes related to the synthesis of interferons such as TLR7 and genetics factors such as single nucleotide polymorphisms (SNPs) or copies number variation (CNV) in the gene have been involved with the development of the disease. The genetic differences between the populations contribute to the complexity of LES. Mexico has a mestizo population with a genetic load of at least three origins: Amerindian, Caucasian, and African. The mestizo of Yucatán is the only group whose contribution Amerindian is mainly Mayan, geographically distant from other Mexican Amerindians. We analyzed the CNV and the frequency of SNP rs179008 of the TLR7 as genetic risk factors in developing the disease in patients from Yucatán and Central Mexico. Results show that 14% of the cases of the Yucatecan population showed significantly >2 CNV and a higher risk of developing the disease (OR: 34.364), concerning 4% of those coming from Central Mexico (OR: 10.855). T allele and the A/T and T/T risk genotypes of rs179008 were more frequent in patients of Central Mexico than in those of Yucatán (50% vs. 30%, 93% vs. 30%, 4% vs. 1%), and association with susceptibility to develop SLE was observed (OR: 1.5 vs. 0.58, 9.54 vs. 0.66, 12 vs. 0.14). Data support the genetic differences between and within Mexican mestizo populations and the role of the TLR7 in the pathogenesis of SLE.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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