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dc.contributor.authorCrespo Facorro, Benedicto 
dc.contributor.authorPrieto, Carlos
dc.contributor.authorSainz Maza, Jesús Vicente
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-02-09T12:11:22Z
dc.date.available2024-02-09T12:11:22Z
dc.date.issued2019
dc.identifier.issn2334-265X
dc.identifier.otherSAF2010-20840-C02-01
dc.identifier.otherSAF2010-20840-C02-01/02
dc.identifier.otherSAF2013-46292-R
dc.identifier.urihttps://hdl.handle.net/10902/31619
dc.description.abstractAntipsychotic drugs are one of the largest types of prescribed drugs. However, antipsychotic-induced weight gain (AIWG) is a major problem for the patients. AIWG increases cardiovascular and cerebrovascular morbidity and mortality, and reduces quality of life and drug compliance. To characterize changes in gene expression related to AIWG, we sequenced total messenger RNA from the blood samples of two groups of schizophrenia patients before and after 3 months of treatment with antipsychotics. The ?weight gain? group was defined by an increase of body mass index (BMI) >1.5 points (18 patients; median BMI increase?=?2.69) and the ?no weight gain? group was defined by a change of BMI between <1.0 and >?1.0 points (18 patients; median BMI increase?=?0.26). We found 115 genes with significant differential expression in the weight gain group before and after medication and 156 in the no weight gain group before and after medication. The weight gain group was significantly enriched with genes related to ?obesity? and ?BMI? (Fisher; p?=?0.0002 and 0.01, respectively) according to the Gene Reference into Function (GeneRIF) database. In the no weight gain group, the enrichment was much smaller (Fisher; p?=?0.02 and 0.79). This study is a first step toward detecting genetic factors that cause AIWG and to generating prediction tests in future studies with larger data sets.es_ES
dc.description.sponsorshipBioinformatics work was partially performed using the Altamira supercomputer (Spanish Supercomputing Network). We thank the Valdecilla Biobank for handling the blood RNA sampling and storage and the CNAG for mRNA sequencing. We also wish to thank the participants and their families for enrolling in this study. C.P. was supported by the PTA fellowship (PTA2015-10483-I) of the Spanish Ministry of Economy, Industry and Competitiveness (MINECO). B.C.-F. was supported by the Ministerio de Ciencia e Innovación (MICINN) in the coordinated project SAF2010-20840-C02-01/02 and by MINECO (SAF2013-46292-R). J.S. was supported by MICINN (SAF2010-20840-C02-01) and by the NIH (5R01HD056465-07; sub-award #320793 from The Children’s Hospital of Philadelphia).es_ES
dc.format.extent8 p.es_ES
dc.language.isoenges_ES
dc.publisherNature Publishing Groupes_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceNPJ Schizophrenia, 2019, 5(1), 7es_ES
dc.titleAltered gene expression in antipsychotic-induced weight gaines_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1038/s41537-019-0075-yes_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1038/s41537-019-0075-y
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International