Morbid Obesity in Women Is Associated with an Altered Intestinal Expression of Genes Related to Cancer Risk and Immune, Defensive, and Antimicrobial Response
Ailec Ho-Plágaro,
Cristina Rodríguez-Díaz,
Concepción Santiago-Fernández,
Carlos López-Gómez,
Sara García-Serrano,
Flores Martín-Reyes,
Francisca Rodríguez-Pacheco,
Alberto Rodríguez-Cañete,
Guillermo Alcaín-Martínez,
Luis Vázquez-Pedreño,
Sergio Valdés,
Lourdes Garrido-Sánchez,
Eduardo García-Fuentes
Affiliations
Ailec Ho-Plágaro
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Cristina Rodríguez-Díaz
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Concepción Santiago-Fernández
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Carlos López-Gómez
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Sara García-Serrano
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Flores Martín-Reyes
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Francisca Rodríguez-Pacheco
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Alberto Rodríguez-Cañete
Unidad de Gestión Clínica de Cirugía General, Digestiva y Trasplantes, Hospital Regional Universitario, 29010 Malaga, Spain
Guillermo Alcaín-Martínez
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Luis Vázquez-Pedreño
Unidad de Gestión Clínica de Aparato Digestivo, Hospital Regional Universitario, 29010 Malaga, Spain
Sergio Valdés
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Lourdes Garrido-Sánchez
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Eduardo García-Fuentes
Instituto de Investigación Biomédica de Málaga-IBIMA, 29010 Malaga, Spain
Background: Little is known about the relation between morbid obesity and duodenal transcriptomic changes. We aimed to identify intestinal genes that may be associated with the development of obesity regardless of the degree of insulin resistance (IR) of patients. Material and Methods: Duodenal samples were assessed by microarray in three groups of women: non-obese women and women with morbid obesity with low and high IR. Results: We identified differentially expressed genes (DEGs) associated with morbid obesity, regardless of IR degree, related to digestion and lipid metabolism, defense response and inflammatory processes, maintenance of the gastrointestinal epithelium, wound healing and homeostasis, and the development of gastrointestinal cancer. However, other DEGs depended on the IR degree. We mainly found an upregulation of genes involved in the response to external organisms, hypoxia, and wound healing functions in women with morbid obesity and low IR. Conclusions: Regardless of the degree of IR, morbid obesity is associated with an altered expression of genes related to intestinal defenses, antimicrobial and immune responses, and gastrointestinal cancer. Our data also suggest a deficient duodenal immune and antimicrobial response in women with high IR.