Exploring the Association between Monoclonal Antibodies and Depression and Suicidal Ideation and Behavior: A VigiBase Study

dc.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorMinnema, Lotte A.
dc.contributor.authorGiezen, Thijs J.
dc.contributor.authorSouverein, Patrick C.
dc.contributor.authorEgberts, Toine C. G.
dc.contributor.authorLeufkens, Hubert G. M.
dc.contributor.authorGardarsdottir, Helga
dc.contributor.departmentLyfjafræðideild (HÍ)en_US
dc.contributor.departmentFaculty of Pharmaceutical Sciences (UI)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.date.accessioned2020-04-03T09:29:34Z
dc.date.available2020-04-03T09:29:34Z
dc.date.issued2019-01-08
dc.descriptionPublisher's version (útgefin grein)en_US
dc.description.abstractIntroduction: Several monoclonal antibodies (mAbs) have been linked to neuropsychiatric adverse efects in patients, including depression and suicidal ideation and behavior. Objective: The aim of this study was to quantify and characterize spontaneously reported adverse drug reactions (ADRs) of depression and suicidal ideation and behavior related to mAb users, and to explore a possible association with their mechanism of action. Methods: We included mAb ADRs that were reported in VigiBase, and identifed those related to depression and suicidal ideation and behavior. Reporting odds ratios (RORs) were estimated for each mAb (bevacizumab as the reference) and according to their infuence on the immune system (not directly targeting [reference], stimulating, or suppressing). Those suppressing the immune system were further divided into their intended indication (auto-immune diseases, cancer). Results: Overall, 2,924,319 ADRs for 44 mAbs were included; 9455 ADRs were related to depression and 1770 were related to suicidal ideation and behavior. The association was strongest for natalizumab and belimumab, both for depression (ROR 5.7, 95% confdence interval [CI] 5.0–6.4; and ROR 5.1, 95% CI 4.2–6.2) and suicidal ideation and behavior (ROR 12.0, 95% CI 7.9–18.3; and ROR 20.2, 95% CI 12.4–33.0). Those suppressing the immune system showed higher ROR, i.e. 1.9 (95% CI 1.8–2.0) for depression and 3.6 (95% CI 3.0–4.4) for suicidal ideation and behavior. This fnding was only seen for mAbs used for treating autoimmune diseases. Conclusion: Depression and suicidal ideation and behavior are seen in patients using mAbs, particularly mAbs used for treating autoimmune diseases that suppress the immune system. For interpretation of these data, the indications for use and other characteristics require further consideration.en_US
dc.description.sponsorshipNo external sources of funding were used to assist in the preparation of this article. The authors would like to thank the Uppsala Monitoring Centre for providing the data.en_US
dc.description.versionPeer Revieweden_US
dc.format.extent887-895en_US
dc.identifier.citationMinnema, L.A., Giezen, T.J., Souverein, P.C. et al. Exploring the Association between Monoclonal Antibodies and Depression and Suicidal Ideation and Behavior: A VigiBase Study. Drug Safety 42, 887–895 (2019). https://doi.org/10.1007/s40264-018-00789-9en_US
dc.identifier.doi10.1007/s40264-018-00789-9
dc.identifier.issn0114-5916
dc.identifier.issn1179-1942 (eISSN)
dc.identifier.journalDrug Safetyen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/1687
dc.language.isoenen_US
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.ispartofseriesDrug Safety;42(7)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectToxicologyen_US
dc.subjectDepressionen_US
dc.subjectmAbsen_US
dc.subjectAutoimmune Diseasesen_US
dc.subjectEiturefnafræðien_US
dc.subjectSjálfsofnæmissjúkdómaren_US
dc.subjectÞunglyndien_US
dc.subjectSjálfsvígen_US
dc.titleExploring the Association between Monoclonal Antibodies and Depression and Suicidal Ideation and Behavior: A VigiBase Studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.licenseOpen Access. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en_US

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