Evidence mapPaperPMID 42169116Full record

ArticleBMC medicine2026

Autoimmune diseases and risk of adverse pregnancy outcomes: a population-based cohort study of five million pregnancies in the UK.

Megha Singh, Anuradhaa Subramanian, Steven Wambua, Neil Cockburn, Stephanie J Hanley, Siang Ing Lee, Arturo Gonzalez-Izquierdo, Mairead Black, John A Reynolds, Francesca L Crowe and 2 more

Abstract read
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Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Megha SinghDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK. m.singh.6@bham.ac.uk.
Anuradhaa SubramanianDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0001-8875-7363
Steven WambuaDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0003-2300-7670
Neil CockburnDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0001-9284-6991
Stephanie J HanleyDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-5260-4450
Siang Ing LeeDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-2332-5452
Arturo Gonzalez-IzquierdoDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-0984-5830
Mairead BlackAberdeen Centre for Women's Health Research, University of Aberdeen, Aberdeen, Aberdeenshire, UK.ORCID http://orcid.org/0000-0002-6841-8601
John A ReynoldsDepartment of Inflammation and Ageing, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-8962-4404
Francesca L CroweDepartment of Applied Health Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0003-4026-1726
Krishnarajah NirantharakumarSchool of Life Course and Population Sciences, King's College London, London, UK.ORCID http://orcid.org/0000-0002-6816-1279
MuM-PreDiCT

Funding

Medical Research Council MR/W014432/1
6 · The paper itself

Abstract

backgroundWith an increasing trend in the prevalence of maternal autoimmune diseases in pregnancy, there is need for evidence on the association between autoimmune diseases and pregnancy outcomes.

methodsThis population-based cohort study used data on pregnancies from primary care practices that contributed to the UK Clinical Practice Research Datalink (CPRD) database (Gold and Aurum) between 2000 and 2022, linked to Hospital Episode Statistics (HES). Modified Poisson regression with robust standard errors estimated adjusted relative risks (aRR) and 95% confidence intervals (95% CI) assessing the association between 17 autoimmune diseases and 12 pregnancy outcomes, selected following literature review and expert consultation. Models were adjusted for demographic and comorbidity variables. Findings were evaluated using the Benjamini-Yekutieli procedure to control for multiple testing across autoimmune disease-outcome associations.

resultsA total of 5,239,383 pregnancies from the CPRD pregnancy register and 2,485,366 births recorded in HES maternity data met the eligibility criteria. Women with autoimmune diseases had an increased risk across all pregnancy outcomes examined. Among antenatal outcomes, markedly elevated risks were observed for hyperemesis gravidarum in Addison's disease (aRR 3.72, 95% CI 2.48-5.59), miscarriage in Sjögren's syndrome (1.66, 1.02-2.70), gestational hypertension in type 1 diabetes mellitus (T1DM; 2.95, 2.77-3.15), pre-eclampsia/eclampsia in T1DM (3.56, 3.32-3.82), and gestational diabetes mellitus in Graves' disease (1.37, 1.21-1.54). For obstetric outcomes, increased risks were observed for caesarean birth in inflammatory bowel disease (IBD; 1.27, 1.22-1.31), small for gestational age in systemic lupus erythematosus (SLE; 2.45, 1.65-3.62), preterm birth in rheumatoid arthritis (1.53, 1.33-1.76), and stillbirth in SLE (1.82, 1.12-1.84). Perinatal mental health outcomes were more common across several autoimmune diseases, with particularly high risks in myasthenia gravis (anxiety 3.05, 1.89-4.92; depression 1.77, 1.37-2.28), SLE (anxiety 2.11, 1.67-2.67; depression 1.36, 1.22-1.53), and multiple sclerosis (anxiety 1.76, 1.38-2.23; depression 1.94, 1.77-2.12). Inverse associations were observed for hyperemesis gravidarum in systemic sclerosis, SLE, and myasthenia gravis, and for hypertensive disorders of pregnancy in multiple sclerosis. After Benjamini-Yekutieli correction for multiple testing, the number of statistically significant associations was reduced, with a core set of robust associations persisting across selected autoimmune diseases particularly, T1DM, SLE, Graves' disease, IBD and key pregnancy outcomes.

conclusionsAutoimmune diseases were associated with increased risks across a wide range of adverse pregnancy outcomes, with marked heterogeneity between individual conditions. This study provides adjusted relative risks across multiple domains of pregnancy outcomes including antenatal (e.g. miscarriage, hyperemesis gravidarum, gestational hypertension, pre-eclampsia, gestational diabetes), obstetric (e.g. preterm birth, caesarean birth, small for gestational age, stillbirth), and perinatal mental health outcomes (anxiety and depression), for both common and less frequently studied autoimmune diseases. The findings highlight the importance of disease-specific evaluation of pregnancy risks.

Indexed as

Autoimmune DiseasesPregnancy ComplicationsPregnancy OutcomeAdultCohort StudiesFemaleHumansPregnancyRisk FactorsUnited KingdomYoung AdultAdverse pregnancy outcomesAutoimmune diseaseCaesarean birthClinical Practice Research DatalinkGestational hypertensionMental healthMiscarriagePreterm birthStillbirthsystemic lupus erythematosusType 1 diabetes

Identifiers

PMID42169116
PMCPMC13374351

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.