TY - JOUR
T1 - Congenital malformations and preeclampsia associated with integrase inhibitor use in pregnancy
T2 - A single-center analysis
AU - CHIP Perinatal Medical Team
AU - Smith, Christiana
AU - Fought, Angela J.
AU - Sung, Joyce F.
AU - McKinney, Jennifer R.
AU - Metz, Torri D.
AU - Fetters, Kirk B.
AU - Lazarus, Sarah
AU - Capraro, Shannon
AU - Barr, Emily
AU - Glenny, Carrie
AU - Buehler, Jenna
AU - Weinberg, Adriana
AU - Din-Nebeil, Megan
AU - Dunn, Jennifer
AU - Ferrero, Phillip
AU - Kinzie, Kay
AU - McFarland, Elizabeth J.
AU - Moor, Jennifer
AU - Navarro, Kacey
AU - Paul, Suzanne
N1 - Publisher Copyright:
© 2023 Smith et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2023/6
Y1 - 2023/6
N2 - Background Antiretroviral therapy (ART) decreases perinatal HIV transmission, but concerns exist regarding maternal and infant safety. We compared the incidence of congenital malformations and other adverse outcomes in pregnancies exposed to integrase inhibitor (INSTI) versus non-INSTI ART. Setting Single-site review of all pregnancies among women living with HIV between 2008 and 2018. Methods We used binomial family generalized estimating equations to model the relationship of congenital anomalies and pregnancy outcomes with exposure to INSTI or dolutegravir (DTG) versus non-INSTI ART. Results Among 257 pregnancies, 77 women received ≥1 INSTI (54 DTG, 14 elvitegravir, 15 raltegravir), 167 received non-INSTI, and 3 had missing data. Fifty congenital anomalies were identified in 36 infants. Infants with first-trimester DTG or any first-trimester INSTI exposure had higher odds of congenital anomalies than infants with first-trimester non-INSTI exposure (OR = 2.55; 95%CI = 1.07–6.10; OR = 2.61; 95%CI = 1.15–5.94, respectively). Infants with INSTI exposure after the second trimester had no increased odds of anomalies. Women with INSTI exposure had higher odds of preeclampsia (OR = 4.73; 95%CI = 1.70–13.19). Among women who received INSTI, grade ≥3 laboratory abnormalities were noted in 2.6% while receiving the INSTI and 3.9% while not receiving the INSTI, versus 16.2% in women who received non-INSTI. There was no association between INSTI exposure and other pregnancy outcomes. Conclusion In our cohort, first-trimester INSTI exposure was associated with increased rates of congenital anomalies and use of INSTI during pregnancy was associated with preeclampsia. These findings underscore the need for continued monitoring of the safety of INSTI in pregnancy.
AB - Background Antiretroviral therapy (ART) decreases perinatal HIV transmission, but concerns exist regarding maternal and infant safety. We compared the incidence of congenital malformations and other adverse outcomes in pregnancies exposed to integrase inhibitor (INSTI) versus non-INSTI ART. Setting Single-site review of all pregnancies among women living with HIV between 2008 and 2018. Methods We used binomial family generalized estimating equations to model the relationship of congenital anomalies and pregnancy outcomes with exposure to INSTI or dolutegravir (DTG) versus non-INSTI ART. Results Among 257 pregnancies, 77 women received ≥1 INSTI (54 DTG, 14 elvitegravir, 15 raltegravir), 167 received non-INSTI, and 3 had missing data. Fifty congenital anomalies were identified in 36 infants. Infants with first-trimester DTG or any first-trimester INSTI exposure had higher odds of congenital anomalies than infants with first-trimester non-INSTI exposure (OR = 2.55; 95%CI = 1.07–6.10; OR = 2.61; 95%CI = 1.15–5.94, respectively). Infants with INSTI exposure after the second trimester had no increased odds of anomalies. Women with INSTI exposure had higher odds of preeclampsia (OR = 4.73; 95%CI = 1.70–13.19). Among women who received INSTI, grade ≥3 laboratory abnormalities were noted in 2.6% while receiving the INSTI and 3.9% while not receiving the INSTI, versus 16.2% in women who received non-INSTI. There was no association between INSTI exposure and other pregnancy outcomes. Conclusion In our cohort, first-trimester INSTI exposure was associated with increased rates of congenital anomalies and use of INSTI during pregnancy was associated with preeclampsia. These findings underscore the need for continued monitoring of the safety of INSTI in pregnancy.
UR - https://www.scopus.com/pages/publications/85163200462
U2 - 10.1371/journal.pone.0276473
DO - 10.1371/journal.pone.0276473
M3 - Article
C2 - 37307279
AN - SCOPUS:85163200462
SN - 1932-6203
VL - 18
JO - PLOS ONE
JF - PLOS ONE
IS - 6 June
M1 - e0276473
ER -