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

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dc.contributor Háskóli Íslands
dc.contributor University of Iceland
dc.contributor.author Minnema, Lotte A.
dc.contributor.author Giezen, Thijs J.
dc.contributor.author Souverein, Patrick C.
dc.contributor.author Egberts, Toine C. G.
dc.contributor.author Leufkens, Hubert G. M.
dc.contributor.author Gardarsdottir, Helga
dc.date.accessioned 2020-04-03T09:29:34Z
dc.date.available 2020-04-03T09:29:34Z
dc.date.issued 2019-01-08
dc.identifier.citation Minnema, 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/s40264-018-00789-9
dc.identifier.issn 0114-5916
dc.identifier.issn 1179-1942 (eISSN)
dc.identifier.uri https://hdl.handle.net/20.500.11815/1687
dc.description Publisher's version (útgefin grein)
dc.description.abstract Introduction: 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.
dc.description.sponsorship No 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.
dc.format.extent 887-895
dc.language.iso en
dc.publisher Springer Science and Business Media LLC
dc.relation.ispartofseries Drug Safety;42(7)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Toxicology
dc.subject Depression
dc.subject mAbs
dc.subject Autoimmune Diseases
dc.subject Eiturefnafræði
dc.subject Sjálfsofnæmissjúkdómar
dc.subject Þunglyndi
dc.subject Sjálfsvíg
dc.title Exploring the Association between Monoclonal Antibodies and Depression and Suicidal Ideation and Behavior: A VigiBase Study
dc.type info:eu-repo/semantics/article
dcterms.license Open 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.
dc.description.version Peer Reviewed
dc.identifier.journal Drug Safety
dc.identifier.doi 10.1007/s40264-018-00789-9
dc.contributor.department Lyfjafræðideild (HÍ)
dc.contributor.department Faculty of Pharmaceutical Sciences (UI)
dc.contributor.school Heilbrigðisvísindasvið (HÍ)
dc.contributor.school School of Health Sciences (UI)


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