Abstract 4370717: Maternal GLP-1 Receptor Agonist Exposure and the Risk of Congenital Cardiovascular Defects: A Global Pharmacovigilance Study

Background: GLP-1 receptor agonists (GLP-1 RAs) are increasingly being recommended to women of reproductive age for the treatment of obesity and type II diabetes. However, their safety profile during early pregnancy is mainly unknown. Congenital cardiovascular defects (CCVDs) are among the most serious and often fatal birth disorders. Understanding the teratogenic danger of GLP-1 RAs becomes more important as their use grows. Objective: To evaluate the association between maternal GLP-1 RA exposure and the risk of CCVDs using global pharmacovigilance data. Methods: A retrospective disproportionality study was conducted using VigiBase, the World Health Organization's worldwide Individual Case Safety Report (ICSR) database, which covered the period from January 2010 to December 2023. Pregnancy-related ICSRs involving GLP-1 RAs were discovered, and Reporting Odds Ratios (RORs) were calculated for CCVDs in comparison to other congenital abnormalities. The analyses were stratified by particular agent (e.g., liraglutide, semaglutide) and trimester of exposure. Sensitivity analysis omitted publications containing known teratogens. Results: There were 112 incidences of CCVD among 7,428 pregnancy-related ICSRs that used GLP-1 RAs. GLP-1 RA exposure was associated with a significantly increased reported risk of CCVDs (ROR: 2.47; 95% CI: 1.97-3.10). Liraglutide provided the most powerful individual signal (ROR: 2.89), followed by semaglutide (ROR: 1.98). Notably, about 85% of CCVD patients were exposed during their first trimester. Sensitivity studies demonstrated that the signal persisted despite removing co-exposures to high-risk teratogens such as ACE inhibitors and retinoids. Conclusion: This pharmacovigilance study discovered a potential safety signal linking first-trimester maternal exposure to GLP-1 RAs with an increased risk of congenital cardiovascular malformations. While causation cannot be established from spontaneous encounters, these results need prospective cohort research and highlight the importance of preconception counseling and contraception planning in women of reproductive potential using GLP-1 RA. These results might influence regulatory recommendations and strengthen pharmacovigilance measures in maternal and fetal care.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4370717
Primary Topic
Gestational Diabetes Research and Management
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article
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article

Abstract 4370717: Maternal GLP-1 Receptor Agonist Exposure and the Risk of Congenital Cardiovascular Defects: A Global Pharmacovigilance Study

Harendra Kumar
Circulation
Gestational Diabetes Research and Management
article

Abstract 4370717: Maternal GLP-1 Receptor Agonist Exposure and the Risk of Congenital Cardiovascular Defects: A Global Pharmacovigilance Study

Harendra Kumar
article en

Abstract

Background: GLP-1 receptor agonists (GLP-1 RAs) are increasingly being recommended to women of reproductive age for the treatment of obesity and type II diabetes. However, their safety profile during early pregnancy is mainly unknown. Congenital cardiovascular defects (CCVDs) are among the most serious and often fatal birth disorders. Understanding the teratogenic danger of GLP-1 RAs becomes more important as their use grows. Objective: To evaluate the association between maternal GLP-1 RA exposure and the risk of CCVDs using global pharmacovigilance data. Methods: A retrospective disproportionality study was conducted using VigiBase, the World Health Organization's worldwide Individual Case Safety Report (ICSR) database, which covered the period from January 2010 to December 2023. Pregnancy-related ICSRs involving GLP-1 RAs were discovered, and Reporting Odds Ratios (RORs) were calculated for CCVDs in comparison to other congenital abnormalities. The analyses were stratified by particular agent (e.g., liraglutide, semaglutide) and trimester of exposure. Sensitivity analysis omitted publications containing known teratogens. Results: There were 112 incidences of CCVD among 7,428 pregnancy-related ICSRs that used GLP-1 RAs. GLP-1 RA exposure was associated with a significantly increased reported risk of CCVDs (ROR: 2.47; 95% CI: 1.97-3.10). Liraglutide provided the most powerful individual signal (ROR: 2.89), followed by semaglutide (ROR: 1.98). Notably, about 85% of CCVD patients were exposed during their first trimester. Sensitivity studies demonstrated that the signal persisted despite removing co-exposures to high-risk teratogens such as ACE inhibitors and retinoids. Conclusion: This pharmacovigilance study discovered a potential safety signal linking first-trimester maternal exposure to GLP-1 RAs with an increased risk of congenital cardiovascular malformations. While causation cannot be established from spontaneous encounters, these results need prospective cohort research and highlight the importance of preconception counseling and contraception planning in women of reproductive potential using GLP-1 RA. These results might influence regulatory recommendations and strengthen pharmacovigilance measures in maternal and fetal care.

CirculationVol. 152(Suppl_3)
Dow University of Health Sciences (PK)
Openalex Percentile: Top 60%
Gestational Diabetes Research and Management
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