Interaction Between the UCP2 rs659366 Polymorphism and Dietary Capsaicin Intake in Relation to the Inflammatory State in Mexican Adults

Metabolic diseases such as obesity and related conditions have an inflammatory basis. Genetic and nutritional factors can influence the development of these diseases by altering the inflammatory state. This study aimed to analyse how the rs659366 (G/A) polymorphism in the <i>UCP2</i> gene interacts with dietary capsaicin (CAP) consumption and affects inflammatory markers in Mexican adults. A cross-sectional, analytical study was conducted in 212 adult patients. The <i>UCP2</i> rs659366 polymorphism was genotyped using an allelic discrimination assay. Dietary CAP intake was measured with a validated food frequency questionnaire. Multivariate linear regression analyses were performed for interaction analyses. The ancestral allele G accounted for 40.2% and the risk allele A accounted for 59.8% of samples. There was a significant interaction between CAP intake and the <i>UCP2</i> rs659366 polymorphism for the inflammatory marker NLR (neutrophil-to-lymphocyte ratio) (<i>p</i> < 0.05). Among subjects with the G allele, higher CAP intake was associated with higher NLR scores (<i>p</i> < 0.001). Patients with the G allele of the <i>UCP2</i> rs659366 polymorphism experienced increased inflammation with higher CAP intake. This finding highlights the need for future studies in personalised nutrition and could expand knowledge about the effects of CAP on obesity and inflammation.

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Journal
International Journal of Molecular Sciences
Published
2025-10-27
DOI
https://doi.org/10.3390/ijms262110419
Primary Topic
Ion Channels and Receptors
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article
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article

Interaction Between the UCP2 rs659366 Polymorphism and Dietary Capsaicin Intake in Relation to the Inflammatory State in Mexican Adults

Genaro Rodríguez‐Uribe, Bertha Landeros-Sánchez, Ana Alondra Sobrevilla-Navarro, Omar Ramos-López et al.
International Journal of Molecular Sciences
Ion Channels and Receptors
article

Interaction Between the UCP2 rs659366 Polymorphism and Dietary Capsaicin Intake in Relation to the Inflammatory State in Mexican Adults

Genaro Rodríguez‐Uribe, Bertha Landeros-Sánchez, Ana Alondra Sobrevilla-Navarro, Omar Ramos-López, José Román Chávez-Méndez
article en

Abstract

Metabolic diseases such as obesity and related conditions have an inflammatory basis. Genetic and nutritional factors can influence the development of these diseases by altering the inflammatory state. This study aimed to analyse how the rs659366 (G/A) polymorphism in the <i>UCP2</i> gene interacts with dietary capsaicin (CAP) consumption and affects inflammatory markers in Mexican adults. A cross-sectional, analytical study was conducted in 212 adult patients. The <i>UCP2</i> rs659366 polymorphism was genotyped using an allelic discrimination assay. Dietary CAP intake was measured with a validated food frequency questionnaire. Multivariate linear regression analyses were performed for interaction analyses. The ancestral allele G accounted for 40.2% and the risk allele A accounted for 59.8% of samples. There was a significant interaction between CAP intake and the <i>UCP2</i> rs659366 polymorphism for the inflammatory marker NLR (neutrophil-to-lymphocyte ratio) (<i>p</i> < 0.05). Among subjects with the G allele, higher CAP intake was associated with higher NLR scores (<i>p</i> < 0.001). Patients with the G allele of the <i>UCP2</i> rs659366 polymorphism experienced increased inflammation with higher CAP intake. This finding highlights the need for future studies in personalised nutrition and could expand knowledge about the effects of CAP on obesity and inflammation.

International Journal of Molecular SciencesVol. 26(21)
Universidad Autónoma de Baja California (MX)
Openalex Percentile: Top 70%
Ion Channels and Receptors
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Interaction Between the UCP2 rs659366 Polymorphism and Dietary Capsaicin Intake in Relation to the Inflammatory State in Mexican Adults — Genaro Rodríguez‐Uribe, Bertha Landeros-Sánchez, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS