Statins and congenital malformations: cohort study

被引:159
|
作者
Bateman, Brian T. [1 ,2 ,3 ]
Hernandez-Diaz, Sonia [4 ]
Fischer, Michael A. [1 ,2 ]
Seely, Ellen W. [5 ]
Ecker, Jeffrey L. [6 ]
Franklin, Jessica M. [1 ,2 ]
Desai, Rishi J. [1 ,2 ]
Allen-Coleman, Cora [1 ,2 ]
Mogun, Helen [1 ,2 ]
Avorn, Jerry [1 ,2 ]
Huybrechts, Krista F. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Div Pharmacoepidemiol & Pharmacoecon, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Obstet Anesthesia,Dept Anesthesia Crit Care &, Boston, MA USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Endocrinol Diabet & Metab,Dept Med, Boston, MA 02115 USA
[6] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Obstet & Gynecol, Boston, MA USA
来源
基金
美国医疗保健研究与质量局;
关键词
MATERNAL EXPOSURE; RISK; PREGNANCY; OUTCOMES; SURVEILLANCE; SIMVASTATIN; PRAVASTATIN; ANOMALIES; SYSTEM; WOMEN;
D O I
10.1136/bmj.h1035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:7
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