ALOX5 , LPA , MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans

Author:

Camacho-Mejorado Rafael1,Gómez Rocío1ORCID,Torres-Sánchez Luisa E.2ORCID,Alhelí Hernández-Tobías Esther3ORCID,Noris Gino4,Santana Carla4,Magaña Jonathan J.5,Orozco Lorena6,de la Peña-Díaz Aurora78ORCID,de la Luz Arenas-Sordo María5,Meraz-Ríos Marco Antonio9ORCID,Majluf-Cruz Abraham10

Affiliation:

1. Departamento de Toxicología, Cinvestav-IPN, Mexico City 07360, Mexico

2. Centro de Investigación en Salud Poblacional, Instituto Nacional de Salud Pública, Cuernavaca, Morelos, Mexico

3. Universidad Autonóma de Nuevo León, Facultad de Salud Pública y Nutrición, Monterrey, Nuevo León, Mexico

4. Laboratorio Biología Molecular Diagnóstica, Querétaro, Qro, Mexico

5. Departmento de Genética, INR, Mexico City, Mexico

6. Laboratorio de Inmunogenómica y Enfermedades Metabólicas, INMEGEN, Mexico City, Mexico

7. Facultad de Medicina, Departamento de Farmacología, Universidad Nacional Autónoma de México, Mexico

8. Departamento de Biología Molecular, Instituto Nacional de Cardiología, Mexico City, Mexico

9. Departamento de Biomedicina Molecular, Cinvestav-IPN, Mexico City, Mexico

10. Unidad de Investigación Médica en Trombosis, Hemostasia y Aterogénesis, IMSS, Mexico City, Mexico

Abstract

Atherothrombosis is the cornerstone of cardiovascular diseases and the primary cause of death worldwide. Genetic contribution to disturbances in lipid metabolism, coagulation, inflammation and oxidative stress increase the susceptibility to its development and progression. Given its multifactorial nature, the multiloci studies have been proposed as potential predictors of susceptibility. A cross-sectional study was conducted to explore the contribution of nine genes involved in oxidative stress, inflammatory and thrombotic processes in 204 subjects with atherothrombosis matched by age and gender with a healthy group ( n = 204). To evaluate the possibility of spurious associations owing to the Mexican population genetic heterogeneity as well as its ancestral origins, 300 unrelated mestizo individuals and 329 Native Americans were also included. ALOX5 , LPA , MMP9 and TPO gene polymorphisms, as well as their multiallelic combinations, were twice to four times more frequent in those individuals with clinical manifestations of atherothrombosis than in the healthy group. Once adjusting for population stratification was done, these differences remained. Our results add further evidence on the contribution of ALOX5 , LPA , MMP9 and TPO polymorphisms to atherothrombosis development in the middle-aged group, emphasizing the multiethnic studies in search of gene risk polymorphisms.

Funder

Consejo Nacional de Ciencia y Tecnología, Conacyt

Consejo Nacional de Ciencia y Tecnología

Publisher

The Royal Society

Subject

Multidisciplinary

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