Esteban Moraga-Escobar

Dr. Esteban Moraga-Escobar

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 December 2021 in International Journal of Sexual Health
Verified
Journal Article
Closed access
CCCarolina Alexandra Adelina Chambi-Martínez
Carolina Alexandra Adelina Chambi-Martínez
EMEsteban Moraga-Escobar
Esteban Moraga-Escobar
GPGonzalo Alberto Peralta-Jiménez
Gonzalo Alberto Peralta-Jiménez
AVAldo Vera-Calzaretta
Aldo Vera-Calzaretta
JBJaime Barrientos
Jaime Barrientos
DPDarío Páez
Darío Páez
To compare the relationships between emotional symptomatology and perceived social support according to gender identity and sexual orientation in LGBTQ+ university students.322 Chilean LGBTQ+ colle...

22 October 2024 in Genes
Verified
Journal Article
Open access
PDF file
AGAlejandra Guzmán-Castillo
Alejandra Guzmán-Castillo
VVVicente Benjamin Vicente
Vicente Benjamin Vicente
KSKristin Schmidt
Kristin Schmidt
EMEsteban Moraga-Escobar
Esteban Moraga-Escobar
RRRomina Andrea Rojas-Ponce
Romina Andrea Rojas-Ponce
JCJuan Luis Castillo-Navarrete
Juan Luis Castillo-Navarrete
Background/Objectives: Post-traumatic stress disorder (PTSD) is a complex condition influenced by both genetic and environmental factors. This longitudinal study aimed to explore the connection between two specific genetic polymorphisms, Val66Met and 5-HTTLPR, and the lifetime prevalence of PTSD in patients from primary care settings. We also examined the role of sociodemographic and psychosocial factors to provide a more comprehensive view of PTSD risk. Methods: We recruited a cohort of primary care patients and diagnosed PTSD using a standardized diagnostic interview. Genetic analyses focused on Val66Met and 5-HTTLPR polymorphisms. We applied logistic regression to assess the association between these genetic markers and PTSD, considering factors such as gender, family history of depression, and experiences of childhood maltreatment. Results: Our findings show that women, individuals with a family history of depression, and those exposed to childhood maltreatment have a higher risk of developing PTSD. While the Val66Met polymorphism was not significantly associated with PTSD, the 5-HTTLPR polymorphism showed a marginal relationship. No significant interaction was found between the two polymorphisms in relation to PTSD. Conclusions: This study underscores the multifactorial nature of PTSD, influenced by both genetic and environmental factors. The findings point to the importance of further research on genetic predispositions and highlight the value of early interventions for high-risk populations in primary care settings.