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Statins and congenital malformations: cohort study
Objective To examine the teratogenic potential of statins. Design Cohort study. Setting United States. Participants A cohort of 886 996 completed pregnancies linked to liveborn infants of women enrolled in Medicaid from 2000 to 2007. Methods We examined the risk of major congenital malformations and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362473/ https://www.ncbi.nlm.nih.gov/pubmed/25784688 http://dx.doi.org/10.1136/bmj.h1035 |
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author | Bateman, Brian T Hernandez-Diaz, Sonia Fischer, Michael A Seely, Ellen W Ecker, Jeffrey L Franklin, Jessica M Desai, Rishi J Allen-Coleman, Cora Mogun, Helen Avorn, Jerry Huybrechts, Krista F |
author_facet | Bateman, Brian T Hernandez-Diaz, Sonia Fischer, Michael A Seely, Ellen W Ecker, Jeffrey L Franklin, Jessica M Desai, Rishi J Allen-Coleman, Cora Mogun, Helen Avorn, Jerry Huybrechts, Krista F |
author_sort | Bateman, Brian T |
collection | PubMed |
description | Objective To examine the teratogenic potential of statins. Design Cohort study. Setting United States. Participants A cohort of 886 996 completed pregnancies linked to liveborn infants of women enrolled in Medicaid from 2000 to 2007. Methods We examined the risk of major congenital malformations and organ specific malformations in offspring associated with maternal use of a statin in the first trimester. Propensity score based methods were used to control for potential confounders, including maternal demographic characteristics, obstetric and medical conditions, and use of other drugs. Results 1152 (0.13%) women used a statin during the first trimester. In unadjusted analyses, the prevalence of malformations in the offspring of these women was 6.34% compared with 3.55% in those of women who did not use a statin in the first trimester (relative risk 1.79, 95% confidence interval 1.43 to 2.23). Controlling for confounders, particularly pre-existing diabetes, accounted for this increase in risk (1.07, 0.85 to 1.37). There were also no statistically significant increases in any of the organ specific malformations assessed after accounting for confounders. Results were similar across a range of sensitivity analyses. Conclusions Our analysis did not find a significant teratogenic effect from maternal use of statins in the first trimester. However, these findings need to be replicated in other large studies, and the long term effects of in utero exposure to statins needs to be assessed, before use of statins in pregnancy can be considered safe. |
format | Online Article Text |
id | pubmed-4362473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43624732015-03-24 Statins and congenital malformations: cohort study Bateman, Brian T Hernandez-Diaz, Sonia Fischer, Michael A Seely, Ellen W Ecker, Jeffrey L Franklin, Jessica M Desai, Rishi J Allen-Coleman, Cora Mogun, Helen Avorn, Jerry Huybrechts, Krista F BMJ Research Objective To examine the teratogenic potential of statins. Design Cohort study. Setting United States. Participants A cohort of 886 996 completed pregnancies linked to liveborn infants of women enrolled in Medicaid from 2000 to 2007. Methods We examined the risk of major congenital malformations and organ specific malformations in offspring associated with maternal use of a statin in the first trimester. Propensity score based methods were used to control for potential confounders, including maternal demographic characteristics, obstetric and medical conditions, and use of other drugs. Results 1152 (0.13%) women used a statin during the first trimester. In unadjusted analyses, the prevalence of malformations in the offspring of these women was 6.34% compared with 3.55% in those of women who did not use a statin in the first trimester (relative risk 1.79, 95% confidence interval 1.43 to 2.23). Controlling for confounders, particularly pre-existing diabetes, accounted for this increase in risk (1.07, 0.85 to 1.37). There were also no statistically significant increases in any of the organ specific malformations assessed after accounting for confounders. Results were similar across a range of sensitivity analyses. Conclusions Our analysis did not find a significant teratogenic effect from maternal use of statins in the first trimester. However, these findings need to be replicated in other large studies, and the long term effects of in utero exposure to statins needs to be assessed, before use of statins in pregnancy can be considered safe. BMJ Publishing Group Ltd. 2015-03-17 /pmc/articles/PMC4362473/ /pubmed/25784688 http://dx.doi.org/10.1136/bmj.h1035 Text en © Bateman et al 2015 http://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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Bateman, Brian T Hernandez-Diaz, Sonia Fischer, Michael A Seely, Ellen W Ecker, Jeffrey L Franklin, Jessica M Desai, Rishi J Allen-Coleman, Cora Mogun, Helen Avorn, Jerry Huybrechts, Krista F Statins and congenital malformations: cohort study |
title | Statins and congenital malformations: cohort study |
title_full | Statins and congenital malformations: cohort study |
title_fullStr | Statins and congenital malformations: cohort study |
title_full_unstemmed | Statins and congenital malformations: cohort study |
title_short | Statins and congenital malformations: cohort study |
title_sort | statins and congenital malformations: cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362473/ https://www.ncbi.nlm.nih.gov/pubmed/25784688 http://dx.doi.org/10.1136/bmj.h1035 |
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