DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results

Albert Martinez-Pinteño,1,* Natalia Rodriguez,1,* Ana Blázquez,2 Maria Teresa Plana,2 Eva Varela,2 Patricia Gassó,1,3 Amalia Lafuente,1,3,4 Luisa Lazaro,2– 5 Sergi Mas1,3,4 1Department of Basic Clinal Practice, Pharmacology Unit, University of Barcelona, Ba...

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Main Authors: Martinez-Pinteño A, Rodriguez N, Blázquez A, Plana MT, Varela E, Gassó P, Lafuente A, Lazaro L, Mas S
Format: Article
Language:English
Published: Dove Medical Press 2021-04-01
Series:Pharmacogenomics and Personalized Medicine
Subjects:
Online Access:https://www.dovepress.com/dna-methylation-of-fluoxetine-response-in-child-and-adolescence-prelim-peer-reviewed-fulltext-article-PGPM
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spelling doaj-c5a2f89bfde94259aa8dcbfdbb2b650c2021-04-20T18:55:25ZengDove Medical PressPharmacogenomics and Personalized Medicine1178-70662021-04-01Volume 1445946764059DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary ResultsMartinez-Pinteño ARodriguez NBlázquez APlana MTVarela EGassó PLafuente ALazaro LMas SAlbert Martinez-Pinteño,1,* Natalia Rodriguez,1,* Ana Blázquez,2 Maria Teresa Plana,2 Eva Varela,2 Patricia Gassó,1,3 Amalia Lafuente,1,3,4 Luisa Lazaro,2– 5 Sergi Mas1,3,4 1Department of Basic Clinal Practice, Pharmacology Unit, University of Barcelona, Barcelona, Spain; 2Department of Child and Adolescent Psychiatry and Psychology, Institute of Neurosciences, Hospital Clinic de Barcelona, Barcelona, Spain; 3Clinical and Experimental Neuroscience Area, The August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; 4G04 Group, Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Carlos III Health Institute, Madrid, Spain; 5Department of Medicine, University of Barcelona, Barcelona, Spain*These authors contributed equally to this workCorrespondence: Sergi MasDepartment of Basic Clinal Practice, Pharmacology Unit, University of Barcelona, Casanova 143, Barcelona, E-08036, SpainTel +34 934024526Fax +34 934035881Email sergimash@ub.eduPurpose: The search for predictors of antidepressant response is gaining increasing attention, with epigenetic markers attracting a great deal of interest. We performed a genome-wide study assessing baseline differences in DNA methylation between Responders and Non-Responders.Patients and Methods: Twenty-two children and adolescents, receiving fluoxetine treatment for the first time, were classified as Responders or Non-Responders according to CGI-I score after 8 weeks of fluoxetine treatment. Genome-wide DNA methylation was profiled using the Illumina Infinium MethylationEPIC BeadChip Kit and analyzed using the Chip Analysis Methylation Pipeline (ChAMP).Results: We identified 21 CpG sites significantly (FDR< 0.05) associated with fluoxetine response that showed meaningful differences (Δβ> ± 0.2) in methylation level between Responders and Non-Responders. Two genes, RHOJ (Ras Homolog Family Member J) and OR2L13 (Olfactory Receptor family 2 subfamily L member 13), presented more than one significant CpG sites.Conclusion: Our findings provide new insights into the molecular mechanisms underlying the complex phenotype of antidepressant response, indicating that methylation at specific genes could be a promising biomarker that needs further replication in large cohorts.Keywords: epigenomics, epigenetics, DNA methylation, pharmacogenetics, antidepressantshttps://www.dovepress.com/dna-methylation-of-fluoxetine-response-in-child-and-adolescence-prelim-peer-reviewed-fulltext-article-PGPMepigenomicsepigeneticsdna methylationpharmacogeneticsantidepressants
collection DOAJ
language English
format Article
sources DOAJ
author Martinez-Pinteño A
Rodriguez N
Blázquez A
Plana MT
Varela E
Gassó P
Lafuente A
Lazaro L
Mas S
spellingShingle Martinez-Pinteño A
Rodriguez N
Blázquez A
Plana MT
Varela E
Gassó P
Lafuente A
Lazaro L
Mas S
DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
Pharmacogenomics and Personalized Medicine
epigenomics
epigenetics
dna methylation
pharmacogenetics
antidepressants
author_facet Martinez-Pinteño A
Rodriguez N
Blázquez A
Plana MT
Varela E
Gassó P
Lafuente A
Lazaro L
Mas S
author_sort Martinez-Pinteño A
title DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
title_short DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
title_full DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
title_fullStr DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
title_full_unstemmed DNA Methylation of Fluoxetine Response in Child and Adolescence: Preliminary Results
title_sort dna methylation of fluoxetine response in child and adolescence: preliminary results
publisher Dove Medical Press
series Pharmacogenomics and Personalized Medicine
issn 1178-7066
publishDate 2021-04-01
description Albert Martinez-Pinteño,1,* Natalia Rodriguez,1,* Ana Blázquez,2 Maria Teresa Plana,2 Eva Varela,2 Patricia Gassó,1,3 Amalia Lafuente,1,3,4 Luisa Lazaro,2– 5 Sergi Mas1,3,4 1Department of Basic Clinal Practice, Pharmacology Unit, University of Barcelona, Barcelona, Spain; 2Department of Child and Adolescent Psychiatry and Psychology, Institute of Neurosciences, Hospital Clinic de Barcelona, Barcelona, Spain; 3Clinical and Experimental Neuroscience Area, The August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; 4G04 Group, Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Carlos III Health Institute, Madrid, Spain; 5Department of Medicine, University of Barcelona, Barcelona, Spain*These authors contributed equally to this workCorrespondence: Sergi MasDepartment of Basic Clinal Practice, Pharmacology Unit, University of Barcelona, Casanova 143, Barcelona, E-08036, SpainTel +34 934024526Fax +34 934035881Email sergimash@ub.eduPurpose: The search for predictors of antidepressant response is gaining increasing attention, with epigenetic markers attracting a great deal of interest. We performed a genome-wide study assessing baseline differences in DNA methylation between Responders and Non-Responders.Patients and Methods: Twenty-two children and adolescents, receiving fluoxetine treatment for the first time, were classified as Responders or Non-Responders according to CGI-I score after 8 weeks of fluoxetine treatment. Genome-wide DNA methylation was profiled using the Illumina Infinium MethylationEPIC BeadChip Kit and analyzed using the Chip Analysis Methylation Pipeline (ChAMP).Results: We identified 21 CpG sites significantly (FDR< 0.05) associated with fluoxetine response that showed meaningful differences (Δβ> ± 0.2) in methylation level between Responders and Non-Responders. Two genes, RHOJ (Ras Homolog Family Member J) and OR2L13 (Olfactory Receptor family 2 subfamily L member 13), presented more than one significant CpG sites.Conclusion: Our findings provide new insights into the molecular mechanisms underlying the complex phenotype of antidepressant response, indicating that methylation at specific genes could be a promising biomarker that needs further replication in large cohorts.Keywords: epigenomics, epigenetics, DNA methylation, pharmacogenetics, antidepressants
topic epigenomics
epigenetics
dna methylation
pharmacogenetics
antidepressants
url https://www.dovepress.com/dna-methylation-of-fluoxetine-response-in-child-and-adolescence-prelim-peer-reviewed-fulltext-article-PGPM
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