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Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus
BACKGROUND: This study aimed to investigate the effect of glucocorticoid doses on adverse pregnancy outcomes (APOs) in women complicated by systemic lupus erythematosus (SLE). METHODS: We investigated 74 pregnancies complicated by SLE or SLE-dominant mixed connective tissue disease. The pregnancies...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722014/ https://www.ncbi.nlm.nih.gov/pubmed/34980235 http://dx.doi.org/10.1186/s13075-021-02699-1 |
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author | Shimada, Hiromi Wakiya, Risa Kanenishi, Kenji Miyatake, Nobuyuki Nakashima, Shusaku Mansour, Mai Mahmoud Fahmy Kato, Mikiya Miyagi, Taichi Sugihara, Koichi Ushio, Yusuke Mino, Rina Mizusaki, Mao Kameda, Tomohiro Kadowaki, Norimitsu Dobashi, Hiroaki |
author_facet | Shimada, Hiromi Wakiya, Risa Kanenishi, Kenji Miyatake, Nobuyuki Nakashima, Shusaku Mansour, Mai Mahmoud Fahmy Kato, Mikiya Miyagi, Taichi Sugihara, Koichi Ushio, Yusuke Mino, Rina Mizusaki, Mao Kameda, Tomohiro Kadowaki, Norimitsu Dobashi, Hiroaki |
author_sort | Shimada, Hiromi |
collection | PubMed |
description | BACKGROUND: This study aimed to investigate the effect of glucocorticoid doses on adverse pregnancy outcomes (APOs) in women complicated by systemic lupus erythematosus (SLE). METHODS: We investigated 74 pregnancies complicated by SLE or SLE-dominant mixed connective tissue disease. The pregnancies were managed from conception to delivery in our institution. We retrospectively evaluated whether the mean glucocorticoid dose during pregnancy is associated with APOs, including preterm birth (PB), low birth weight (LBW), and light-for-date (LFD). We also calculated the cut-off dose of glucocorticoid that affected APOs. RESULTS: All APOs occurred in 35 (50.7%) patients, with 14 cases of PB, 23 cases of LBW, and 10 cases of LFD. Patients with all APOs or PB had a higher dose of glucocorticoid during pregnancy than patients without all APOs or with full-term birth (P = 0.03, P < 0.01, respectively). Logistic regression analysis for all APOs and PB showed that the cut-off values of the mean glucocorticoid dose were 6.5 and 10.0 mg/day, respectively. Patients who delivered LBW or LFD newborns showed no significant difference in the glucocorticoid dose used during pregnancy than patients without LBW or LFD newborns. Patients who delivered LBW newborns were more likely to have used glucocorticoids during pregnancy (P < 0.01). CONCLUSIONS: In pregnancies complicated by SLE, a relatively lower dose of glucocorticoid than previously reported is significantly related to APOs, especially PB. Therefore, the disease activity of patients with SLE should be managed with the appropriate lower dose of glucocorticoid during pregnancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02699-1. |
format | Online Article Text |
id | pubmed-8722014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87220142022-01-06 Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus Shimada, Hiromi Wakiya, Risa Kanenishi, Kenji Miyatake, Nobuyuki Nakashima, Shusaku Mansour, Mai Mahmoud Fahmy Kato, Mikiya Miyagi, Taichi Sugihara, Koichi Ushio, Yusuke Mino, Rina Mizusaki, Mao Kameda, Tomohiro Kadowaki, Norimitsu Dobashi, Hiroaki Arthritis Res Ther Research Article BACKGROUND: This study aimed to investigate the effect of glucocorticoid doses on adverse pregnancy outcomes (APOs) in women complicated by systemic lupus erythematosus (SLE). METHODS: We investigated 74 pregnancies complicated by SLE or SLE-dominant mixed connective tissue disease. The pregnancies were managed from conception to delivery in our institution. We retrospectively evaluated whether the mean glucocorticoid dose during pregnancy is associated with APOs, including preterm birth (PB), low birth weight (LBW), and light-for-date (LFD). We also calculated the cut-off dose of glucocorticoid that affected APOs. RESULTS: All APOs occurred in 35 (50.7%) patients, with 14 cases of PB, 23 cases of LBW, and 10 cases of LFD. Patients with all APOs or PB had a higher dose of glucocorticoid during pregnancy than patients without all APOs or with full-term birth (P = 0.03, P < 0.01, respectively). Logistic regression analysis for all APOs and PB showed that the cut-off values of the mean glucocorticoid dose were 6.5 and 10.0 mg/day, respectively. Patients who delivered LBW or LFD newborns showed no significant difference in the glucocorticoid dose used during pregnancy than patients without LBW or LFD newborns. Patients who delivered LBW newborns were more likely to have used glucocorticoids during pregnancy (P < 0.01). CONCLUSIONS: In pregnancies complicated by SLE, a relatively lower dose of glucocorticoid than previously reported is significantly related to APOs, especially PB. Therefore, the disease activity of patients with SLE should be managed with the appropriate lower dose of glucocorticoid during pregnancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02699-1. BioMed Central 2022-01-03 2022 /pmc/articles/PMC8722014/ /pubmed/34980235 http://dx.doi.org/10.1186/s13075-021-02699-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Article Shimada, Hiromi Wakiya, Risa Kanenishi, Kenji Miyatake, Nobuyuki Nakashima, Shusaku Mansour, Mai Mahmoud Fahmy Kato, Mikiya Miyagi, Taichi Sugihara, Koichi Ushio, Yusuke Mino, Rina Mizusaki, Mao Kameda, Tomohiro Kadowaki, Norimitsu Dobashi, Hiroaki Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title | Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title_full | Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title_fullStr | Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title_full_unstemmed | Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title_short | Preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
title_sort | preterm birth is strongly affected by the glucocorticoid dose during pregnancy in women complicated by systemic lupus erythematosus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722014/ https://www.ncbi.nlm.nih.gov/pubmed/34980235 http://dx.doi.org/10.1186/s13075-021-02699-1 |
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