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Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study
OBJECTIVES: To evaluate the association of paternal intake of antipsychotics, anxiolytics, hypnotics and sedatives, antidepressants, selective serotonin reuptake inhibitors (SSRIs) and (benzo)diazepines during the development of fertilising sperm with birth defects in offspring. DESIGN: Prospective...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968542/ https://www.ncbi.nlm.nih.gov/pubmed/35354621 http://dx.doi.org/10.1136/bmjopen-2021-053946 |
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author | Wensink, Maarten Lu, Ying Tian, Lu Jensen, Tina Kold Skakkebæk, Niels Erik Lindahl-Jacobsen, Rune Eisenberg, Michael |
author_facet | Wensink, Maarten Lu, Ying Tian, Lu Jensen, Tina Kold Skakkebæk, Niels Erik Lindahl-Jacobsen, Rune Eisenberg, Michael |
author_sort | Wensink, Maarten |
collection | PubMed |
description | OBJECTIVES: To evaluate the association of paternal intake of antipsychotics, anxiolytics, hypnotics and sedatives, antidepressants, selective serotonin reuptake inhibitors (SSRIs) and (benzo)diazepines during the development of fertilising sperm with birth defects in offspring. DESIGN: Prospective registry-based cohort study. SETTING: Total Danish birth cohort 1997–2016 using Danish national registries. PARTICIPANTS: All 1 201 119 Danish liveborn singletons born 1997–2016 were eligible, 39 803 (3.3%) of whom had at least one major birth defect. EXPOSURE: Offspring were considered exposed if their father had filled at least one prescription in the relevant drug category during development of fertilising sperm (the 3 months prior to conception). PRIMARY AND SECONDARY OUTCOME MEASURES: Primary outcome was the diagnosis, in the first year of life, of at least one major birth defect as categorised in the EUROCAT guidelines. Secondary outcome was the diagnosis, in the first year of life, of at least one major birth defect in any of the EUROCAT subcategories. Adjusted ORs (AORs) were calculated, along with their 95% CIs, adjusted for year, education, smoking status and age of the mother, and education, disposable income and age of the father. RESULTS: This study found weak or null associations between birth defects and selected drugs. Specifically, antidepressants (17 827 exposed births) gave 3.5% birth defects (AOR 0.97 (0.89 to 1.05)). Diazepines, oxazepines, thiazepines and oxepines (as antipsychotics, 1633 offspring) gave 4.7% birth defects (AOR 1.22 (0.97 to 1.54)), attenuated to 1.13 when excluding by mothers’ prescriptions. The study was well powered assuming 100% therapy adherence, while assuming 50% therapy adherence, the study remained well powered for the largest groups (SSRIs and antidepressants overall). CONCLUSIONS: Antipsychotics, anxiolytics, hypnotics and sedatives, antidepressants, SSRIs and benzodiazepine-derived anxiolytics, when taken by the father during development of fertilising sperm, are generally safe with regard to birth defects. |
format | Online Article Text |
id | pubmed-8968542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-89685422022-04-20 Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study Wensink, Maarten Lu, Ying Tian, Lu Jensen, Tina Kold Skakkebæk, Niels Erik Lindahl-Jacobsen, Rune Eisenberg, Michael BMJ Open Reproductive Medicine OBJECTIVES: To evaluate the association of paternal intake of antipsychotics, anxiolytics, hypnotics and sedatives, antidepressants, selective serotonin reuptake inhibitors (SSRIs) and (benzo)diazepines during the development of fertilising sperm with birth defects in offspring. DESIGN: Prospective registry-based cohort study. SETTING: Total Danish birth cohort 1997–2016 using Danish national registries. PARTICIPANTS: All 1 201 119 Danish liveborn singletons born 1997–2016 were eligible, 39 803 (3.3%) of whom had at least one major birth defect. EXPOSURE: Offspring were considered exposed if their father had filled at least one prescription in the relevant drug category during development of fertilising sperm (the 3 months prior to conception). PRIMARY AND SECONDARY OUTCOME MEASURES: Primary outcome was the diagnosis, in the first year of life, of at least one major birth defect as categorised in the EUROCAT guidelines. Secondary outcome was the diagnosis, in the first year of life, of at least one major birth defect in any of the EUROCAT subcategories. Adjusted ORs (AORs) were calculated, along with their 95% CIs, adjusted for year, education, smoking status and age of the mother, and education, disposable income and age of the father. RESULTS: This study found weak or null associations between birth defects and selected drugs. Specifically, antidepressants (17 827 exposed births) gave 3.5% birth defects (AOR 0.97 (0.89 to 1.05)). Diazepines, oxazepines, thiazepines and oxepines (as antipsychotics, 1633 offspring) gave 4.7% birth defects (AOR 1.22 (0.97 to 1.54)), attenuated to 1.13 when excluding by mothers’ prescriptions. The study was well powered assuming 100% therapy adherence, while assuming 50% therapy adherence, the study remained well powered for the largest groups (SSRIs and antidepressants overall). CONCLUSIONS: Antipsychotics, anxiolytics, hypnotics and sedatives, antidepressants, SSRIs and benzodiazepine-derived anxiolytics, when taken by the father during development of fertilising sperm, are generally safe with regard to birth defects. BMJ Publishing Group 2022-03-29 /pmc/articles/PMC8968542/ /pubmed/35354621 http://dx.doi.org/10.1136/bmjopen-2021-053946 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Reproductive Medicine Wensink, Maarten Lu, Ying Tian, Lu Jensen, Tina Kold Skakkebæk, Niels Erik Lindahl-Jacobsen, Rune Eisenberg, Michael Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title | Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title_full | Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title_fullStr | Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title_full_unstemmed | Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title_short | Nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
title_sort | nervous system drugs taken by future fathers and birth defects in offspring: a prospective registry-based cohort study |
topic | Reproductive Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968542/ https://www.ncbi.nlm.nih.gov/pubmed/35354621 http://dx.doi.org/10.1136/bmjopen-2021-053946 |
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