Integrase inhibitor drugs during pregnancy and congenital anomalies: A case/non-case study from the global pharmacovigilance database VigiBase®

被引:0
|
作者
Saint-Lary, Laura [1 ]
Lacroix, Isabelle [1 ,2 ]
Leroy, Valeriane [1 ]
Sommet, Agnes [1 ,2 ]
机构
[1] Univ Paul Sabatier III, Univ Toulouse, CERPOP, Inserm, Toulouse, France
[2] Univ Toulouse 3, Serv Pharmacol Clin, CHU Toulouse, Toulouse, France
来源
PHARMACOLOGY RESEARCH & PERSPECTIVES | 2024年 / 12卷 / 04期
关键词
antiretroviral drugs; case/non-case study; congenital anomalies; HIV; integrase inhibitors; pregnancy; HIV-INFECTED WOMEN; ANTIRETROVIRAL THERAPY; BIRTH-DEFECTS; UNITED-KINGDOM; EXPOSURE; DOLUTEGRAVIR; INFANTS; SAFETY; BORN; RALTEGRAVIR;
D O I
10.1002/prp2.1247
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In 2018, a significant neural tube defects (NTD) signal was reported after pre-conceptional exposure to dolutegravir, but was not confirmed in further analysis. Since 2019, dolutegravir-based regimen, an integrase inhibitor (INI), is recommended by WHO as the most-effective first-line therapy in all patients living with HIV. To explore the potential INI-related teratogenic effect, we searched disproportionate signals between exposure to INI-class drugs and congenital anomalies, compared to non-INI drugs, using the international pharmacovigilance database, VigiBase (R). We selected all the reports registered in VigiBase (R) between 01/01/2007 and 30/03/2021 on any antiretroviral drug-related fetal or neonatal adverse drug reactions, declared either in children (<2 years) exposed in utero or in pregnant women (12-50 years). A case/non-case study was conducted to detected signals between congenital anomalies and prenatal exposure to any INI-class drug, compared to non-INI drugs, by estimating adjusted reporting odds ratios (aROR) with 95% confidence intervals (95%CI). We identified 2521 unique reports, among which 664 (26.3%) were related to INI-class use. Overall, 520 congenital anomalies were cited from 327 unique reports, of whom 31.0% were INI-related. Compared to non-INI drugs, no significant disproportionate reporting signal between prenatal exposure to INI-class drugs and congenital anomalies was found (aROR 1.13; 95% CI:0.85-1.51). However, specific significant signals were reported for raltegravir/elvitegravir/dolutegravir drug exposure and urinary malformations (aROR 2.43; 95%CI:1.08-5.43), digestive malformations (aROR 3.09; 95%CI:1.22-7.84), and NTDs (aROR 3.02; 95%CI:1.09-8.37). Although specific congenital anomalies signals associated with raltegravir/elvitegravir/dolutegravir exposure were notified, causal relationship needs to be further investigated in prospective studies.
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页数:12
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