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Adverse birth outcomes and early-life infections after in utero exposure to corticosteroids for inflammatory bowel disease: a Danish nationwide cohort study
Systemic corticosteroids are often used to treat inflammatory bowel disease (IBD) flares during pregnancy as maintenance of disease remission is crucial to optimize pregnancy outcomes. However, there is little data regarding the effect of in utero exposure to corticosteroids on the risk of adverse b...
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Published in: | BMC medicine 2023-04, Vol.21 (1), p.140-140, Article 140 |
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description | Systemic corticosteroids are often used to treat inflammatory bowel disease (IBD) flares during pregnancy as maintenance of disease remission is crucial to optimize pregnancy outcomes. However, there is little data regarding the effect of in utero exposure to corticosteroids on the risk of adverse birth outcomes and early-life infections in the offspring.
We used the Danish national registries to establish a nationwide cohort of all singleton live births in women with IBD from 1995 to 2015. Outcomes in children exposed in utero to corticosteroids were compared to those who were not exposed. In logistic and Cox proportional hazard regression models, we adjusted the outcomes (major congenital malformation, preterm birth, small for gestational age, low 5-min Apgar score, and infections) for confounders such as body mass index, smoking, comorbidity, and additional medical IBD treatment.
After in utero exposure to corticosteroids at any time between 30 days prior to conception through the first trimester (n = 707), the adjusted hazard ratio of major congenital malformation was 1.28 (95% CI: 0.82-2.00) compared to children born to women with IBD, but not exposed to corticosteroids in utero (n = 9371). After in utero exposure to corticosteroids at any time during pregnancy (n = 1336), the adjusted odds ratios for preterm birth, small for gestational age, and low 5-min Apgar score were 2.45 (95% CI: 1.91-3.13), 1.21 (95% CI: 0.76-1.90), and 0.91 (95% CI: 0.33-2.52), respectively. Finally, the adjusted hazard ratio of overall infections in the first year of life was 1.14 (95% CI: 0.94-1.39).
This nationwide cohort study suggests that children of women with IBD exposed to corticosteroids in utero had an almost 2.5-fold increased risk of preterm birth. Use of corticosteroids is closely related to disease activity and we cannot adjust for the independent role of disease activity. It is however reassuring that the other examined birth and early-life outcomes were not statistically significantly increased. |
doi_str_mv | 10.1186/s12916-023-02817-7 |
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We used the Danish national registries to establish a nationwide cohort of all singleton live births in women with IBD from 1995 to 2015. Outcomes in children exposed in utero to corticosteroids were compared to those who were not exposed. In logistic and Cox proportional hazard regression models, we adjusted the outcomes (major congenital malformation, preterm birth, small for gestational age, low 5-min Apgar score, and infections) for confounders such as body mass index, smoking, comorbidity, and additional medical IBD treatment.
After in utero exposure to corticosteroids at any time between 30 days prior to conception through the first trimester (n = 707), the adjusted hazard ratio of major congenital malformation was 1.28 (95% CI: 0.82-2.00) compared to children born to women with IBD, but not exposed to corticosteroids in utero (n = 9371). After in utero exposure to corticosteroids at any time during pregnancy (n = 1336), the adjusted odds ratios for preterm birth, small for gestational age, and low 5-min Apgar score were 2.45 (95% CI: 1.91-3.13), 1.21 (95% CI: 0.76-1.90), and 0.91 (95% CI: 0.33-2.52), respectively. Finally, the adjusted hazard ratio of overall infections in the first year of life was 1.14 (95% CI: 0.94-1.39).
This nationwide cohort study suggests that children of women with IBD exposed to corticosteroids in utero had an almost 2.5-fold increased risk of preterm birth. Use of corticosteroids is closely related to disease activity and we cannot adjust for the independent role of disease activity. It is however reassuring that the other examined birth and early-life outcomes were not statistically significantly increased.</description><identifier>ISSN: 1741-7015</identifier><identifier>EISSN: 1741-7015</identifier><identifier>DOI: 10.1186/s12916-023-02817-7</identifier><identifier>PMID: 37046314</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adrenal Cortex Hormones - adverse effects ; Apgar score ; Birth ; Birth defects ; Birth outcomes ; Birth weight ; Body mass ; Body mass index ; Body size ; Child ; Children ; Cohort analysis ; Cohort Studies ; Comorbidity ; Complications and side effects ; Congenital defects ; Congenital diseases ; Congenital malformations ; Corticoids ; Corticosteroids ; Demographic aspects ; Denmark - epidemiology ; Dosage and administration ; Drug therapy ; Exposure ; Female ; Gestational age ; Health risks ; Human exposure ; Humans ; In utero exposure ; Infant, Newborn ; Infection ; Infections ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - drug therapy ; Inflammatory Bowel Diseases - epidemiology ; Intestine ; Intrauterine exposure ; Offspring ; Pediatrics ; Pregnancy ; Pregnancy Complications - drug therapy ; Pregnancy Complications - epidemiology ; Pregnancy Outcome - epidemiology ; Premature birth ; Premature Birth - epidemiology ; Prenatal development ; Preterm birth ; Regression analysis ; Regression models ; Remission ; Risk factors ; Small for gestational age ; Steroids ; Womens health</subject><ispartof>BMC medicine, 2023-04, Vol.21 (1), p.140-140, Article 140</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-a0e241453bfd740bca5a022501a66f99d7c7790a40e51a562696ade2ef1a586f3</citedby><cites>FETCH-LOGICAL-c595t-a0e241453bfd740bca5a022501a66f99d7c7790a40e51a562696ade2ef1a586f3</cites><orcidid>0000-0002-7634-6812 ; 0000-0002-2720-4404 ; 0000-0002-7433-7656 ; 0000-0002-4598-8679 ; 0000-0002-9514-3033</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091841/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2803010925?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37046314$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jølving, Line Riis</creatorcontrib><creatorcontrib>Nielsen, Jan</creatorcontrib><creatorcontrib>Andersen, Mette Louise</creatorcontrib><creatorcontrib>Friedman, Sonia</creatorcontrib><creatorcontrib>Nørgård, Bente Mertz</creatorcontrib><title>Adverse birth outcomes and early-life infections after in utero exposure to corticosteroids for inflammatory bowel disease: a Danish nationwide cohort study</title><title>BMC medicine</title><addtitle>BMC Med</addtitle><description>Systemic corticosteroids are often used to treat inflammatory bowel disease (IBD) flares during pregnancy as maintenance of disease remission is crucial to optimize pregnancy outcomes. However, there is little data regarding the effect of in utero exposure to corticosteroids on the risk of adverse birth outcomes and early-life infections in the offspring.
We used the Danish national registries to establish a nationwide cohort of all singleton live births in women with IBD from 1995 to 2015. Outcomes in children exposed in utero to corticosteroids were compared to those who were not exposed. In logistic and Cox proportional hazard regression models, we adjusted the outcomes (major congenital malformation, preterm birth, small for gestational age, low 5-min Apgar score, and infections) for confounders such as body mass index, smoking, comorbidity, and additional medical IBD treatment.
After in utero exposure to corticosteroids at any time between 30 days prior to conception through the first trimester (n = 707), the adjusted hazard ratio of major congenital malformation was 1.28 (95% CI: 0.82-2.00) compared to children born to women with IBD, but not exposed to corticosteroids in utero (n = 9371). After in utero exposure to corticosteroids at any time during pregnancy (n = 1336), the adjusted odds ratios for preterm birth, small for gestational age, and low 5-min Apgar score were 2.45 (95% CI: 1.91-3.13), 1.21 (95% CI: 0.76-1.90), and 0.91 (95% CI: 0.33-2.52), respectively. Finally, the adjusted hazard ratio of overall infections in the first year of life was 1.14 (95% CI: 0.94-1.39).
This nationwide cohort study suggests that children of women with IBD exposed to corticosteroids in utero had an almost 2.5-fold increased risk of preterm birth. Use of corticosteroids is closely related to disease activity and we cannot adjust for the independent role of disease activity. It is however reassuring that the other examined birth and early-life outcomes were not statistically significantly increased.</description><subject>Adrenal Cortex Hormones - adverse effects</subject><subject>Apgar score</subject><subject>Birth</subject><subject>Birth defects</subject><subject>Birth outcomes</subject><subject>Birth weight</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Body size</subject><subject>Child</subject><subject>Children</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Comorbidity</subject><subject>Complications and side effects</subject><subject>Congenital defects</subject><subject>Congenital diseases</subject><subject>Congenital malformations</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>Demographic aspects</subject><subject>Denmark - epidemiology</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Exposure</subject><subject>Female</subject><subject>Gestational age</subject><subject>Health risks</subject><subject>Human exposure</subject><subject>Humans</subject><subject>In utero exposure</subject><subject>Infant, Newborn</subject><subject>Infection</subject><subject>Infections</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory Bowel Diseases - drug therapy</subject><subject>Inflammatory Bowel Diseases - epidemiology</subject><subject>Intestine</subject><subject>Intrauterine exposure</subject><subject>Offspring</subject><subject>Pediatrics</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - drug therapy</subject><subject>Pregnancy Complications - epidemiology</subject><subject>Pregnancy Outcome - epidemiology</subject><subject>Premature birth</subject><subject>Premature Birth - epidemiology</subject><subject>Prenatal development</subject><subject>Preterm birth</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Remission</subject><subject>Risk factors</subject><subject>Small for gestational age</subject><subject>Steroids</subject><subject>Womens health</subject><issn>1741-7015</issn><issn>1741-7015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt9uFCEUxidGY2v1BbwwJCbGm6nAwDDjTdPUf02aeKPXhIHDDpuZYQWmdd_Fh5XZrXXXGEKAc77zIxy-onhJ8DkhTf0uEtqSusS0yrMhohSPilMiGCkFJvzxwf6keBbjGmPKhWBPi5NKYFZXhJ0Wvy7NLYQIqHMh9cjPSfsRIlKTQaDCsC0HZwG5yYJOzk85YxOEHEBzXj2Cnxsf5wAoeaR9SE77uCScicj6RWgHNY4q-bBFnb-DARkXQUV4jxT6oCYXezSphX3nDGRGnykoptlsnxdPrBoivLhfz4rvnz5-u_pS3nz9fH11eVNq3vJUKgyUEcarzhrBcKcVV5hSjomqa9u2RmghWqwYBk4Ur2nd1soABZtPTW2rs-J6zzVereUmuFGFrfTKyV3Ah5VUy8sGkI1gHQHRMs4saxi0xlaUE6qFzkdqMutiz9rM3QhGw5SCGo6gx5nJ9XLlbyXBuCUNI5nw9p4Q_I8ZYpKjixqGQU3g5yhpg3FNRdM2Wfr6H-naz2HKvVpUFSa4pfyvaqXyC_KH-HyxXqDyUuS2Ccaq5drz_6jyMDDmT53Auhw_KnhzUNCDGlIf_TDvbHIspHuhDj7GAPahGwTLxcly72SZnSx3TpYiF7067ONDyR_rVr8B-drvWw</recordid><startdate>20230412</startdate><enddate>20230412</enddate><creator>Jølving, Line Riis</creator><creator>Nielsen, Jan</creator><creator>Andersen, Mette Louise</creator><creator>Friedman, Sonia</creator><creator>Nørgård, Bente Mertz</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7634-6812</orcidid><orcidid>https://orcid.org/0000-0002-2720-4404</orcidid><orcidid>https://orcid.org/0000-0002-7433-7656</orcidid><orcidid>https://orcid.org/0000-0002-4598-8679</orcidid><orcidid>https://orcid.org/0000-0002-9514-3033</orcidid></search><sort><creationdate>20230412</creationdate><title>Adverse birth outcomes and early-life infections after in utero exposure to corticosteroids for inflammatory bowel disease: a Danish nationwide cohort study</title><author>Jølving, Line Riis ; Nielsen, Jan ; Andersen, Mette Louise ; Friedman, Sonia ; Nørgård, Bente Mertz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c595t-a0e241453bfd740bca5a022501a66f99d7c7790a40e51a562696ade2ef1a586f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adrenal Cortex Hormones - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jølving, Line Riis</au><au>Nielsen, Jan</au><au>Andersen, Mette Louise</au><au>Friedman, Sonia</au><au>Nørgård, Bente Mertz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adverse birth outcomes and early-life infections after in utero exposure to corticosteroids for inflammatory bowel disease: a Danish nationwide cohort study</atitle><jtitle>BMC medicine</jtitle><addtitle>BMC Med</addtitle><date>2023-04-12</date><risdate>2023</risdate><volume>21</volume><issue>1</issue><spage>140</spage><epage>140</epage><pages>140-140</pages><artnum>140</artnum><issn>1741-7015</issn><eissn>1741-7015</eissn><abstract>Systemic corticosteroids are often used to treat inflammatory bowel disease (IBD) flares during pregnancy as maintenance of disease remission is crucial to optimize pregnancy outcomes. However, there is little data regarding the effect of in utero exposure to corticosteroids on the risk of adverse birth outcomes and early-life infections in the offspring.
We used the Danish national registries to establish a nationwide cohort of all singleton live births in women with IBD from 1995 to 2015. Outcomes in children exposed in utero to corticosteroids were compared to those who were not exposed. In logistic and Cox proportional hazard regression models, we adjusted the outcomes (major congenital malformation, preterm birth, small for gestational age, low 5-min Apgar score, and infections) for confounders such as body mass index, smoking, comorbidity, and additional medical IBD treatment.
After in utero exposure to corticosteroids at any time between 30 days prior to conception through the first trimester (n = 707), the adjusted hazard ratio of major congenital malformation was 1.28 (95% CI: 0.82-2.00) compared to children born to women with IBD, but not exposed to corticosteroids in utero (n = 9371). After in utero exposure to corticosteroids at any time during pregnancy (n = 1336), the adjusted odds ratios for preterm birth, small for gestational age, and low 5-min Apgar score were 2.45 (95% CI: 1.91-3.13), 1.21 (95% CI: 0.76-1.90), and 0.91 (95% CI: 0.33-2.52), respectively. Finally, the adjusted hazard ratio of overall infections in the first year of life was 1.14 (95% CI: 0.94-1.39).
This nationwide cohort study suggests that children of women with IBD exposed to corticosteroids in utero had an almost 2.5-fold increased risk of preterm birth. Use of corticosteroids is closely related to disease activity and we cannot adjust for the independent role of disease activity. It is however reassuring that the other examined birth and early-life outcomes were not statistically significantly increased.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37046314</pmid><doi>10.1186/s12916-023-02817-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7634-6812</orcidid><orcidid>https://orcid.org/0000-0002-2720-4404</orcidid><orcidid>https://orcid.org/0000-0002-7433-7656</orcidid><orcidid>https://orcid.org/0000-0002-4598-8679</orcidid><orcidid>https://orcid.org/0000-0002-9514-3033</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal Cortex Hormones - adverse effects Apgar score Birth Birth defects Birth outcomes Birth weight Body mass Body mass index Body size Child Children Cohort analysis Cohort Studies Comorbidity Complications and side effects Congenital defects Congenital diseases Congenital malformations Corticoids Corticosteroids Demographic aspects Denmark - epidemiology Dosage and administration Drug therapy Exposure Female Gestational age Health risks Human exposure Humans In utero exposure Infant, Newborn Infection Infections Inflammatory bowel disease Inflammatory bowel diseases Inflammatory Bowel Diseases - drug therapy Inflammatory Bowel Diseases - epidemiology Intestine Intrauterine exposure Offspring Pediatrics Pregnancy Pregnancy Complications - drug therapy Pregnancy Complications - epidemiology Pregnancy Outcome - epidemiology Premature birth Premature Birth - epidemiology Prenatal development Preterm birth Regression analysis Regression models Remission Risk factors Small for gestational age Steroids Womens health |
title | Adverse birth outcomes and early-life infections after in utero exposure to corticosteroids for inflammatory bowel disease: a Danish nationwide cohort study |
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