Mostrar el registro sencillo del ítem

dc.creatorSaucedo‐Uribe, Erasmoes_ES
dc.creatorGenis‐Mendoza, Alma Deliaes_ES
dc.creatorDíaz‐Anzaldúa, Adrianaes_ES
dc.creatorMartínez‐Magaña, José Jaimees_ES
dc.creatorTovilla‐Zarate, Carlos Alfonsoes_ES
dc.creatorJuárez‐Rojop, Iselaes_ES
dc.creatorLanzagorta, Nuriaes_ES
dc.creatorEscamilla, Michaeles_ES
dc.creatorGonzález‐Castro, Thelma Beatrizes_ES
dc.creatorLópez Narvaez, María Liliaes_ES
dc.creatorHernández‐Díaz, Yazmínes_ES
dc.creatorNicolini, Humbertoes_ES
dc.date2019
dc.date.accessioned2023-01-17T20:38:49Z
dc.date.available2023-01-17T20:38:49Z
dc.date.issued2019
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/7668
dc.identifier.urihttps://doi.org/10.1002/brb3.1249
dc.descriptionIntroduction: Several studies indicate that polygenic obesity is linked to fat‐mass and obesity‐associated (FTO) genetic variants. Nevertheless, the link between variants in FTO and mental disorders has been barely explored. The present work aims to deter‐ mine whether FTO genetic variants are associated with bipolar disorder and obesity, and to perform an in silico prediction of variant‐dependent functional impact on the developing brain transcriptome. Methods: Four hundred and forty‐six Mexican mestizos were included in a genetic association analysis. SNP‐sequence kernel association test and linear mixed models were implemented for genetic association assessment. For functional impact predic‐ tion, we analyzed the mapping of regulatory elements, the modification of binding sites of transcription factors and the expression of transcription factors in the brain developing transcriptome, searching on different databases. Results: In the set‐based analysis, we found different associated regions to BD (bipo‐ lar disorder) and obesity. The promoter flanking region of FTO intron 1 was associ‐ ated with differential effects on BMI, while intron 2 of RPGRIP1L and FTO upstream regions were associated with BD. The prediction analysis showed that FTO BD‐asso‐ ciated variants disturb binding sites of SP1 and SP2; obesity‐associated variants, on the other hand, disturb binding sites of FOXP1, which are transcription factors highly expressed during prenatal development stages of the brain. Conclusion: Our results suggest a possible effect of FTO variants on neurodevelop‐ ment in obesity and bipolar disorder, which gives new insights into the molecular mechanism underlying this association.
dc.formatPDF
dc.language.isoeng
dc.publisherJohn Wileyi & Sons
dc.relation9(6)e01249
dc.rightsAcceso Cerrado
dc.titleDifferential effects on neurodevelopment of FTO variants in obesity and bipolar disorder suggested by in silico prediction of functional impact: An analysis in Mexican populationes_ES
dc.typeArtículo
dc.contributor.affiliationCenter of Advanced Neurosciences, Department of Psychiatry, Autonomous University of Nuevo Leon, Hospital Universitario “Dr. José Eleuterio González”, Monterrey, Mexico
dc.contributor.emailnicolini_humberto@yahoo.com (Humberto Nicolini)
dc.relation.jnabreviadoBRAIN BEHAV
dc.relation.journalBrain and Behavior
dc.identifier.placeEstados Unidos
dc.date.published2019
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñiz
dc.identifier.eissn2162-3279
dc.identifier.doi10.1002/brb3.1249
dc.subject.kwBipolar disorder
dc.subject.kwFTO variants
dc.subject.kwIn silico functional prediction
dc.subject.kwNeurodevelopment


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem