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Sjögren’s syndrome and pregnancy: a Portuguese case-control study

INTRODUCTION: Pregnancy in patients with autoimmune disorders is associated with an increased risk of adverse outcomes. Sjögren’s syndrome (SS) is one of the most common among autoimmune diseases. Presently data regarding the impact of SS on obstetric outcomes are scarce and inconclusive. This study...

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Autores principales: Barros, Tânia, Braga, Jorge, Abreu, Maria Inês, Brandão, Mariana, Farinha, Fátima, Marinho, António, Braga, António
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661414/
https://www.ncbi.nlm.nih.gov/pubmed/36381208
http://dx.doi.org/10.5114/reum.2022.120754
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author Barros, Tânia
Braga, Jorge
Abreu, Maria Inês
Brandão, Mariana
Farinha, Fátima
Marinho, António
Braga, António
author_facet Barros, Tânia
Braga, Jorge
Abreu, Maria Inês
Brandão, Mariana
Farinha, Fátima
Marinho, António
Braga, António
author_sort Barros, Tânia
collection PubMed
description INTRODUCTION: Pregnancy in patients with autoimmune disorders is associated with an increased risk of adverse outcomes. Sjögren’s syndrome (SS) is one of the most common among autoimmune diseases. Presently data regarding the impact of SS on obstetric outcomes are scarce and inconclusive. This study aims to evaluate the impact of SS on maternal-fetal and neonatal outcomes compared with pregnancy outcomes in the general population. MATERIAL AND METHODS: A retrospective case-control study included 26 pregnancies in SS patients and a healthy control group (CG), followed in a Portuguese tertiary center, between 2015 and 2020. Baseline maternal data were collected, and maternal-fetal and neonatal outcomes were evaluated. Statistical analysis used SPSS 25.0, and a p-value of 0.05 was considered statistically significant. RESULTS: All pregnancies occurred after the diagnosis of SS, with a mean exposure time between diagnosis and pregnancy of 4.92 ±2.78 years. In the SS group, the incidence of ANA, anti-Ro/SSA, and anti-La/SSB antibodies positivity was 80.8%, 61.5%, and 46.2%, respectively. Hydroxychloroquine (HCQ) was used in 57.7%. Miscarriage was significantly higher in the SS group (19.2% vs. 1.8%, p < 0.01). There was a higher prevalence of fetal growth restriction (OR 11.16, 95% CI: 0.96–129.26). Preterm delivery (9.5% vs. 5.6%, p = 0.503) and mean birth weight (2998.16 g vs. 3155.79 g, p = 0.178) did not differ significantly between the groups. In the SS group, admission to the neonatal intensive care unit (NICU) rate was increased (OR 71.67, 95% CI: 3.78–1357.16). Three pregnancies were complicated by congenital heart block (CHB) (14.3% vs. 0%, p = 0.015). In all cases, the diagnosis was performed during second trimester of pregnancy, and betamethasone was administered. CONCLUSIONS: Women with SS had a significantly higher incidence of miscarriage, admission to NICU, and CHB than controls. Congenital heart block was the most critical condition that affects the offspring of mothers with SS. Successful pregnancy in the study group was possible with prenatal monitoring and a multidisciplinary approach.
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spelling pubmed-96614142022-11-14 Sjögren’s syndrome and pregnancy: a Portuguese case-control study Barros, Tânia Braga, Jorge Abreu, Maria Inês Brandão, Mariana Farinha, Fátima Marinho, António Braga, António Reumatologia Original Paper INTRODUCTION: Pregnancy in patients with autoimmune disorders is associated with an increased risk of adverse outcomes. Sjögren’s syndrome (SS) is one of the most common among autoimmune diseases. Presently data regarding the impact of SS on obstetric outcomes are scarce and inconclusive. This study aims to evaluate the impact of SS on maternal-fetal and neonatal outcomes compared with pregnancy outcomes in the general population. MATERIAL AND METHODS: A retrospective case-control study included 26 pregnancies in SS patients and a healthy control group (CG), followed in a Portuguese tertiary center, between 2015 and 2020. Baseline maternal data were collected, and maternal-fetal and neonatal outcomes were evaluated. Statistical analysis used SPSS 25.0, and a p-value of 0.05 was considered statistically significant. RESULTS: All pregnancies occurred after the diagnosis of SS, with a mean exposure time between diagnosis and pregnancy of 4.92 ±2.78 years. In the SS group, the incidence of ANA, anti-Ro/SSA, and anti-La/SSB antibodies positivity was 80.8%, 61.5%, and 46.2%, respectively. Hydroxychloroquine (HCQ) was used in 57.7%. Miscarriage was significantly higher in the SS group (19.2% vs. 1.8%, p < 0.01). There was a higher prevalence of fetal growth restriction (OR 11.16, 95% CI: 0.96–129.26). Preterm delivery (9.5% vs. 5.6%, p = 0.503) and mean birth weight (2998.16 g vs. 3155.79 g, p = 0.178) did not differ significantly between the groups. In the SS group, admission to the neonatal intensive care unit (NICU) rate was increased (OR 71.67, 95% CI: 3.78–1357.16). Three pregnancies were complicated by congenital heart block (CHB) (14.3% vs. 0%, p = 0.015). In all cases, the diagnosis was performed during second trimester of pregnancy, and betamethasone was administered. CONCLUSIONS: Women with SS had a significantly higher incidence of miscarriage, admission to NICU, and CHB than controls. Congenital heart block was the most critical condition that affects the offspring of mothers with SS. Successful pregnancy in the study group was possible with prenatal monitoring and a multidisciplinary approach. Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2022-11-04 2022 /pmc/articles/PMC9661414/ /pubmed/36381208 http://dx.doi.org/10.5114/reum.2022.120754 Text en Copyright: © 2022 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Barros, Tânia
Braga, Jorge
Abreu, Maria Inês
Brandão, Mariana
Farinha, Fátima
Marinho, António
Braga, António
Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title_full Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title_fullStr Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title_full_unstemmed Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title_short Sjögren’s syndrome and pregnancy: a Portuguese case-control study
title_sort sjögren’s syndrome and pregnancy: a portuguese case-control study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661414/
https://www.ncbi.nlm.nih.gov/pubmed/36381208
http://dx.doi.org/10.5114/reum.2022.120754
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