# The C/C Genotype of the C-1019G (rs6295) Polymorphism of the 5-HT1A Receptor Gene Is Associated with Lower Susceptibility to Depressive Symptoms in a Rural Population in Mexico

**Authors:** Margarita Hernandez-Mixteco, Olga Lidia Valenzuela, Cecilia Luz Balderas-Vazquez, Paola Castillo-Juárez, Sandra Rivera-Gutiérrez, Rocío Liliana García-Reyes, Gilberto Cornejo-Estudillo, Ricardo Jiovanni Soria-Herrera, Moises León-Juárez, Addy Cecilia Helguera-Repetto, Daniel Valencia-Trujillo, Victoria Campos-Peña, Eliud Alfredo Garcia-Montalvo, Jorge Francisco Cerna-Cortés

PMC · DOI: 10.3390/neurolint17060087 · Neurology International · 2025-05-31

## TL;DR

This study found that the C/C genotype of a serotonin receptor gene variant is linked to lower risk of depressive symptoms in a rural Mexican population.

## Contribution

The study identifies a protective genetic variant (C/C genotype of rs6295) against depressive symptoms in a rural Mexican population.

## Key findings

- The C/C genotype was more common in the control group than in individuals with depressive symptoms.
- The protective effect of the C/C genotype was particularly observed among men.
- The C/C genotype is associated with decreased risk of depressive symptomatology.

## Abstract

Background: Depression is one of the most prevalent mental health disorders worldwide, affecting a significant proportion of the global population. Its etiology is complex and influenced by the interaction of environmental factors and genetic variations. In Mexico, it has been reported that 41.3% of the population exhibits depressive symptoms. Previous studies have suggested that susceptibility to depression may be associated with the C-1019G (rs6295) polymorphism in the serotonin 1A (5-HT1A) receptor gene. Objective: In this study, we aimed to evaluate the association between the C-1019G polymorphism and depressive symptoms in a rural Mexican population. Methods: Using polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP), we examined the effect of C-1019G on depression symptoms, as evaluated by the Beck Depression Inventory. Data were obtained from 83 volunteers; individuals with depressive symptoms and those with a healthy mood were compared. Results: The results showed that the homozygous C/C genotype was found significantly more frequently in the control group than in individuals with depressive symptoms, particularly among men, and is thus associated with a decreased risk of depressive symptomatology. Conclusions: The C/C genotype could protect against susceptibility to developing depressive symptoms in a rural population in Mexico.

## Linked entities

- **Genes:** HTR1A (5-hydroxytryptamine receptor 1A) [NCBI Gene 3350]
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** HTR1A (5-hydroxytryptamine receptor 1A) [NCBI Gene 3350] {aka 5-HT-1A, 5-HT1A, 5HT1a, ADRB2RL1, ADRBRL1, G-21}
- **Diseases:** Depression (MESH:D003866), mental health disorders (OMIM:603663)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C-1019G

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12196349/full.md

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Source: https://tomesphere.com/paper/PMC12196349