TY - JOUR
T1 - Antiretroviral drug exposure in pregnancy and risk of congenital anomalies
T2 - a European case/non-case malformed study
AU - Saint-Lary, Laura
AU - Beau, Anna Belle
AU - Sommet, Agnès
AU - Leroy, Valériane
AU - Loane, Maria
AU - Cavero-Carbonell, Clara
AU - Garne, Ester
AU - Hoareau, Jonathan
AU - Bielenska, Anna Latos
AU - Monier, Isabelle
AU - Nelen, Vera
AU - Neville, Amanda J.
AU - O’Mahony, Mary
AU - Perthus, Isabelle
AU - Pierini, Anna
AU - Rissmann, Anke
AU - Rouget, Florence
AU - Sichitiu, Joanna
AU - Tucker, David
AU - Dolk, Helen
AU - Damase-Michel, Christine
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/2/26
Y1 - 2025/2/26
N2 - Purpose: Antiretroviral drugs are recommended during pregnancy to achieve HIV viral suppression and reduce mother-to-child transmission. Congenital anomaly signals were reported after fetal exposure to antiretroviral drugs in several studies warranting further investigation. We aimed to evaluate the risk of congenital anomalies after fetal exposure to antiretroviral drugs using the European congenital anomaly registry data. Methods: A case/non-case study was performed, using the EUROmediCAT central database. All the congenital anomalies, exposed to any antiretroviral drugs, were included from 1995 to 2019. We explored each signal identified from the literature for associations between congenital anomalies and specific antiretroviral exposures. We compared antiretroviral exposure between the signal anomalies (cases) and all other malformed registrations (controls). Reporting odds ratio (ROR) and their 95% confidence intervals were estimated and adjusted for registry and maternal age. Results: Between 1995 and 2019, 173 cases of congenital anomalies were observed after any exposure to antiretroviral drugs. The signal previously identified in the literature between congenital heart defects and exposure to zidovudine was confirmed in the main analysis (aROR 3.66 [1.63–8.23]). Other signals identified in the literature were not confirmed, although two cases of hypospadias and two cases of limb defects were reported after zidovudine and atazanavir exposure, respectively. The signal detection analysis did not reveal any new signal after applying the Bonferroni correction. Conclusions: Our study does not reveal new signals but confirms the previously identified signal between congenital heart defects and fetal exposure to zidovudine. The physio-pathological hypothesis induced by zidovudine exposure should be explored in future studies.
AB - Purpose: Antiretroviral drugs are recommended during pregnancy to achieve HIV viral suppression and reduce mother-to-child transmission. Congenital anomaly signals were reported after fetal exposure to antiretroviral drugs in several studies warranting further investigation. We aimed to evaluate the risk of congenital anomalies after fetal exposure to antiretroviral drugs using the European congenital anomaly registry data. Methods: A case/non-case study was performed, using the EUROmediCAT central database. All the congenital anomalies, exposed to any antiretroviral drugs, were included from 1995 to 2019. We explored each signal identified from the literature for associations between congenital anomalies and specific antiretroviral exposures. We compared antiretroviral exposure between the signal anomalies (cases) and all other malformed registrations (controls). Reporting odds ratio (ROR) and their 95% confidence intervals were estimated and adjusted for registry and maternal age. Results: Between 1995 and 2019, 173 cases of congenital anomalies were observed after any exposure to antiretroviral drugs. The signal previously identified in the literature between congenital heart defects and exposure to zidovudine was confirmed in the main analysis (aROR 3.66 [1.63–8.23]). Other signals identified in the literature were not confirmed, although two cases of hypospadias and two cases of limb defects were reported after zidovudine and atazanavir exposure, respectively. The signal detection analysis did not reveal any new signal after applying the Bonferroni correction. Conclusions: Our study does not reveal new signals but confirms the previously identified signal between congenital heart defects and fetal exposure to zidovudine. The physio-pathological hypothesis induced by zidovudine exposure should be explored in future studies.
KW - Antiretroviral drug
KW - Congenital anomalies
KW - First trimester exposure
KW - HIV
KW - Pregnancy
U2 - 10.1007/s00228-025-03814-w
DO - 10.1007/s00228-025-03814-w
M3 - Journal article
C2 - 40011239
AN - SCOPUS:85218793777
SN - 0031-6970
JO - European Journal of Clinical Pharmacology
JF - European Journal of Clinical Pharmacology
ER -