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Utilization of topiramate during pregnancy and risk of birth defects
Mark W Green1, John D Seeger, Craig Peterson
1Mount Sinai School of Medicine, New York, NY, USA. mark.green@mssm.edu
Insights
This study found that topiramate use during pregnancy showed little to no increased risk of oral clefts or major congenital malformations compared to other anti-epileptic drugs or certain medical conditions. However, small event numbers limit definitive conclusions on topiramate risks.
Area of Science:
- Obstetrics and Gynecology
- Pharmacology
- Teratology
Background:
- Topiramate is an anti-epileptic drug (AED) with potential teratogenic risks.
- Evaluating fetal exposure risks to medications during pregnancy is crucial for maternal and child health.
Purpose of the Study:
- To assess the risk of oral cleft and major congenital malformations in infants exposed to topiramate during the first trimester of pregnancy.
- To compare these risks against exposure to other AEDs and maternal conditions like epilepsy, migraine, and diabetes.
Main Methods:
- A retrospective study utilizing pharmacy and medical claims data from 2002-2010.
- Identified infants exposed to topiramate (n=870) and other AEDs (n=3615) in the first trimester.
- Compared outcomes with infants born to mothers with migraine (n=26,865), epilepsy (n=2607), diabetes (n=13,062), and a random sample (n=99,761).
- Calculated unadjusted relative risks and 95% confidence intervals.
Main Results:
- Oral cleft frequency: 0.23% with topiramate vs. 0.17%-0.31% in comparators (RR 0.75-1.47).
- Major malformation frequency: 4.33% with topiramate vs. 3.21%-6.58% in comparators (RR 0.65-1.33).
- Relative risks for topiramate exposure did not show a statistically significant increase compared to most comparator groups.
Conclusions:
- Topiramate exposure in early pregnancy appears to carry little to no increased risk for oral clefts or major congenital malformations compared to other AEDs or specific maternal conditions.
- The study's findings are limited by the small number of observed events, warranting cautious interpretation.
- Further research with larger cohorts is needed to strengthen inferences regarding topiramate's safety profile in pregnancy.
Objective:
To evaluate the risk of oral cleft and major congenital malformation occurrence in infants born to women exposed to topiramate in their first trimester of pregnancy compared with women who used other anti-epileptic drugs or those with disease states in which topiramate may have been used.
Methods:
Sourced from patients' pharmacy and medical claims from 2002 through 2010, this study identified infants born from mothers exposed to topiramate (n = 870) and other anti-epileptic drugs (n = 3615) in the first trimester of pregnancy. First trimester exposure was based on prescription dispensing dates and days supplied relative to infant birth date, accounting for premature delivery. Infants born to women with migraine without epilepsy (n = 26,865), women with epilepsy (n = 2607), and women with diabetes mellitus (n = 13,062), as well as randomly sampled women (n = 99,761), were used for comparison. Topiramate use was excluded from all groups with the exception of the topiramate and random sample cohorts. Non-anti-epileptic drug teratogens were excluded from each cohort (except random sample). Unadjusted relative risks and 95% confidence intervals for topiramate vs each comparator were calculated. Risks >1 indicate a higher risk with topiramate vs comparator, whereas risks <1 indicate a lower risk with topiramate vs comparator.
Results:
The frequency of oral clefts was 0.23% for topiramate use, 0.17% for other anti-epileptic drug use (topiramate vs comparator relative risk = 1.39 [95% confidence interval: 0.28-6.85]), 0.16% for migraineurs (1.47 [0.36-6.06]), 0.31% for epileptics (0.75 [0.16-3.52]), 0.26% for diabetics (0.88 [0.21-3.67]), and 0.16% for the random sample (1.44 [0.36-5.81]). The frequency of major congenital malformations was 4.33% for topiramate use, 3.21% for other anti-epileptic drugs (1.33 [0.92-1.90]), 3.79% for migraineurs (1.12 [0.81-1.55]), 4.33% for epileptics (0.98 [0.68-1.41]), 6.58% for diabetics (0.65 [0.47-0.89]), and 3.77% for the random sample (1.13 [0.82-1.55]).
Conclusions:
This retrospective study quantified the association between topiramate exposure during pregnancy and the risk of oral cleft or major congenital malformations, and suggested little or no increase in risk in comparison with exposure to other anti-epileptic drugs or to disease states, such as migraine, epilepsy, or diabetes. However, small numbers of events limit the strength of inferences.
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