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dc.creatorBerlanga, Carlos
dc.creatorMendieta, Danelia
dc.creatorAlva, Guadalupe
dc.creatorLara, María del Carmen
dc.date.accessioned2017-06-29T04:30:23Z
dc.date.available2017-06-29T04:30:23Z
dc.date.issued2003es_ES
dc.identifier396es_ES
dc.identifier.issn1540-9996es_ES
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/5087
dc.identifier.urihttps://doi.org/10.1089/154099903321154121es_ES
dc.language.isoenges_ES
dc.relation21 (1) 33-39 p.es_ES
dc.relationversión del editores_ES
dc.rightsacceso cerradoes_ES
dc.titleFailure of tibolone to potentiate the pharmacological effect of fluoxetine in postmenopausal major depressiones_ES
dc.typearticlees_ES
dc.contributor.affiliationNational Institute of Psychiatry, Ramón de la Fuente Clinical Research Divisiones_ES
dc.contributor.emailcisnerb@imp.edu.mxes_ES
dc.relation.jnabreviadoJ WOMENS HEALTHes_ES
dc.relation.journalJournal of women's healthes_ES
dc.identifier.placeEstados Unidoses_ES
dc.date.published2003es_ES
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñizes_ES
dc.description.monthEne-Febes_ES
dc.description.abstractotrodiomaBACKGROUND: Perimenopausal depression has been attributed to physiological progressive estrogen decline. Estrogen and derivatives have some mood-enhancing effects, although studies of using estrogen as an antidepressant have had mixed results. The gonadomimetic drug tibolone stimulates estrogen receptors in a tissue-selective fashion, increasing the gonadal activity without causing some of the usual side effects of other estrogen preparations. METHODS: A total of 31 postmenopausal outpatients with a major depressive disorder (MDD) participated in the study. Sixteen received the antidepressant fluoxetine (20 mg/day) plus tibolone (2.5 mg/day), and 15 received the same dose of fluoxetine plus placebo, assigned in a randomized fashion. RESULTS: After 8 weeks of treatment, the two groups had a similar level of improvement in their depressive symptoms. Both treatments were well tolerated, without significant side effects. Pretreatment and posttreatment serum hormonal levels did not predict the final response. CONCLUSIONS: Combining tibolone and fluoxetine did not represent a more robust antidepressant response than fluoxetine alone in postmenopausal women with MDD.es_ES
dc.subject.meshmAgedes_ES
dc.subject.meshmDepressive Disorderes_ES
dc.subject.meshmbloodes_ES
dc.subject.meshmdrug therapyes_ES
dc.subject.meshmDouble-Blind Methodes_ES
dc.subject.meshmEstrogen Receptor Modulatorses_ES
dc.subject.meshmtherapeutic usees_ES
dc.subject.meshmEstrogenses_ES
dc.subject.meshmFemalees_ES
dc.subject.meshmFluoxetinees_ES
dc.subject.meshmtherapeutic usees_ES
dc.subject.meshmHumanses_ES
dc.subject.meshmMexicoes_ES
dc.subject.meshmMiddle Agedes_ES
dc.subject.meshmNorpregneneses_ES
dc.subject.meshmPostmenopausees_ES
dc.subject.meshmSerotonin Uptake Inhibitorses_ES


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