Rare Functional Variants Associated with Antidepressant Remission in Mexican-Americans: Short title: Antidepressant remission and pharmacogenetics in Mexican-Americans

ABSTRACT: Introduction: Rare genetic functional variants can contribute to 30-40% of functional variability in genes relevant to drug action. Therefore, we investigated the role of rare functional variants in antidepressant response. Method: Mexican-American individuals meeting the Diagnostic and St...

Full description

Autores:
Arcos Burgos, Oscar Mauricio
Wong, Ma Li
Liu, Sha
Licinio, Alice W.
Yu, Chenglong
Chin, Eunice W. M.
Yao, Wei Dong
Lu, Xin Yun
Bornstein, Stefan R.
Licinio, Julio
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/42122
Acceso en línea:
https://hdl.handle.net/10495/42122
Palabra clave:
Antidepressive Agents
Antidepresivos
Depressive Disorder, Major
Trastorno Depresivo Mayor
Double-Blind Method
Método Doble Ciego
Pharmacogenetics
Farmacogenética
Prospective Studies
Estudios Prospectivos
Treatment Outcome
Resultado del Tratamiento
Americanos Mexicanos
Mexican Americans
https://id.nlm.nih.gov/mesh/D000928
https://id.nlm.nih.gov/mesh/D003865
https://id.nlm.nih.gov/mesh/D004311
https://id.nlm.nih.gov/mesh/D010597
https://id.nlm.nih.gov/mesh/D011446
https://id.nlm.nih.gov/mesh/D016896
https://id.nlm.nih.gov/mesh/D017058
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Description
Summary:ABSTRACT: Introduction: Rare genetic functional variants can contribute to 30-40% of functional variability in genes relevant to drug action. Therefore, we investigated the role of rare functional variants in antidepressant response. Method: Mexican-American individuals meeting the Diagnostic and Statistical Manual-IV criteria for major depressive disorder (MDD) participated in a prospective randomized, double-blind study with desipramine or fluoxetine. The rare variant analysis was performed using whole-exome genotyping data. Network and pathway analyses were carried out with the list of significant genes. Results: The Kernel-Based Adaptive Cluster method identified functional rare variants in 35 genes significantly associated with treatment remission (False discovery rate, FDR <0.01). Pathway analysis of these genes supports the involvement of the following gene ontology processes: olfactory/sensory transduction, regulation of response to cytokine stimulus, and meiotic cell cycleprocess. Limitations: Our study did not have a placebo arm. We were not able to use antidepressant blood level as a covariate. Our study is based on a small sample size of only 65 Mexican-American individuals. Further studies using larger cohorts are warranted. Conclusion: Our data identified several rare functional variants in antidepressant drug response in MDD patients. These have the potential to serve as genetic markers for predicting drug response.