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The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus

OBJECTIVES: Systemic lupus erythematosus (SLE) is an autoimmune disease that can lead to unfavorable pregnancy complications in women. This study aimed to evaluate the factors associated with pregnancy outcomes in patients with SLE. RESULTS: Fifty-nine pregnant women with SLE (121 pregnancies) parti...

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Autores principales: Zamani, Batool, Shayestehpour, Mohammad, Esfahanian, Farifteh, Akbari, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108499/
https://www.ncbi.nlm.nih.gov/pubmed/32228711
http://dx.doi.org/10.1186/s13104-020-05039-9
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author Zamani, Batool
Shayestehpour, Mohammad
Esfahanian, Farifteh
Akbari, Hossein
author_facet Zamani, Batool
Shayestehpour, Mohammad
Esfahanian, Farifteh
Akbari, Hossein
author_sort Zamani, Batool
collection PubMed
description OBJECTIVES: Systemic lupus erythematosus (SLE) is an autoimmune disease that can lead to unfavorable pregnancy complications in women. This study aimed to evaluate the factors associated with pregnancy outcomes in patients with SLE. RESULTS: Fifty-nine pregnant women with SLE (121 pregnancies) participated in this retrospective cohort study. The mean age of the patients was 33.74 ± 3.80 years (range 21 to 48 years). Fetal loss occurred in 43.8% of pregnancies. The most common laboratory findings in SLE patients were antinuclear antibody (81.4%) and anti-ds DNA positivity (54.2%). High levels of C-reactive protein (CRP) during pregnancy, renal involvement, anti-double-stranded DNA positivity, anti-phospholipid antibody (APA) positivity and younger age at disease onset were significantly correlated with unfavourable pregnancy outcomes. A significant difference was observed between duration of SLE and low birth weight (P = 0.003), pre-eclampsia (P = 0.012) and still birth (P = 0.036). High CRP, APA positivity, anti-dsDNA positivity and kidney involvement were predictors of adverse pregnancy outcomes in SLE patients. Renal involvement increased risk of pregnancy with complication 8.5 times (OR = 8.5, 95% CI 1.396–63.373, P = 0.017). Antiphospholipid syndrome (APS) also was associated with an odds ratio of 5.18 (95% CI 1.681–13.647, P = 0.001).
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spelling pubmed-71084992020-04-07 The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus Zamani, Batool Shayestehpour, Mohammad Esfahanian, Farifteh Akbari, Hossein BMC Res Notes Research Note OBJECTIVES: Systemic lupus erythematosus (SLE) is an autoimmune disease that can lead to unfavorable pregnancy complications in women. This study aimed to evaluate the factors associated with pregnancy outcomes in patients with SLE. RESULTS: Fifty-nine pregnant women with SLE (121 pregnancies) participated in this retrospective cohort study. The mean age of the patients was 33.74 ± 3.80 years (range 21 to 48 years). Fetal loss occurred in 43.8% of pregnancies. The most common laboratory findings in SLE patients were antinuclear antibody (81.4%) and anti-ds DNA positivity (54.2%). High levels of C-reactive protein (CRP) during pregnancy, renal involvement, anti-double-stranded DNA positivity, anti-phospholipid antibody (APA) positivity and younger age at disease onset were significantly correlated with unfavourable pregnancy outcomes. A significant difference was observed between duration of SLE and low birth weight (P = 0.003), pre-eclampsia (P = 0.012) and still birth (P = 0.036). High CRP, APA positivity, anti-dsDNA positivity and kidney involvement were predictors of adverse pregnancy outcomes in SLE patients. Renal involvement increased risk of pregnancy with complication 8.5 times (OR = 8.5, 95% CI 1.396–63.373, P = 0.017). Antiphospholipid syndrome (APS) also was associated with an odds ratio of 5.18 (95% CI 1.681–13.647, P = 0.001). BioMed Central 2020-03-30 /pmc/articles/PMC7108499/ /pubmed/32228711 http://dx.doi.org/10.1186/s13104-020-05039-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Zamani, Batool
Shayestehpour, Mohammad
Esfahanian, Farifteh
Akbari, Hossein
The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title_full The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title_fullStr The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title_full_unstemmed The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title_short The study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
title_sort study of factors associated with pregnancy outcomes in patients with systemic lupus erythematosus
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108499/
https://www.ncbi.nlm.nih.gov/pubmed/32228711
http://dx.doi.org/10.1186/s13104-020-05039-9
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