Evidence map›Paper›PMID 39191479›Full record

ArticleInternational journal of epidemiology2024

Pregnancy complications and new-onset maternal autoimmune disease.

Natalie V Scime, Sonia M Grandi, Joel G Ray, Cindy-Lee Dennis, Mary A De Vera, Hailey R Banack, Simone N Vigod, Alexa Boblitz, Hilary K Brown

Abstract read
In one paragraph

Article in International journal of epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Natalie V ScimeDepartment of Health and Society, University of Toronto Scarborough, Toronto, Ontario, Canada.ORCID 0000-0002-5811-7661
Sonia M GrandiChild Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-8576-7854
Joel G RayICES, Toronto, Ontario, Canada.
Cindy-Lee DennisLi Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, Ontario, Canada.
Mary A De VeraFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-2205-2683
Hailey R BanackDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-6230-2245
Simone N VigodICES, Toronto, Ontario, Canada.
Alexa BoblitzICES, Toronto, Ontario, Canada.
Hilary K BrownDepartment of Health and Society, University of Toronto Scarborough, Toronto, Ontario, Canada.ORCID 0000-0002-8690-5841

Funding

CIHR
6 · The paper itself

Abstract

backgroundAutoimmune diseases disproportionately impact women and female-specific aspects of reproduction are thought to play a role. We investigated the time-varying association between pregnancy complications and new-onset autoimmune disease in females during the reproductive and midlife years.

methodsWe conducted a population-based cohort study of 1 704 553 singleton births to 1 072 445 females in Ontario, Canada (2002-17) with no pre-existing autoimmune disease. Pregnancy complications were preeclampsia, stillbirth, spontaneous preterm birth and severe small for gestational age (SGA). Royston-Parmar models were used to estimate the time-varying association between pregnancy complications and a composite of 25 autoimmune diseases from date of delivery to date of autoimmune disease diagnosis or censoring at death, loss of health insurance, or 31 March 2021. Models were adjusted for baseline socio-demographics, parity and comorbidities.

resultsAt 19 years (median = 10.9 years of follow-up), cumulative incidence of autoimmune disease was 3.1% in those with a pregnancy complication and 2.6% in those without complications. Adjusted hazard ratio (AHR) curves as a function of time since birth were generally L-shaped. Universally, risks were most elevated within the first 3 years after birth [at 1 year: preeclampsia AHR 1.22, 95% confidence interval (CI) 1.09-1.36; stillbirth AHR 1.36, 95% CI 0.99-1.85; spontaneous preterm birth AHR 1.30, 95% CI 1.18-1.44; severe SGA AHR 1.14, 95% CI 0.99-1.31] and plateaued but remained elevated thereafter.

conclusionsPrior history of pregnancy complications may be an important female-specific risk factor to consider during clinical assessment of females for possible autoimmune disease to facilitate timely detection and treatment.

Indexed as

Autoimmune DiseasesPregnancy ComplicationsAdultCohort StudiesFemaleHumansIncidenceInfant, NewbornInfant, Small for Gestational AgeMiddle AgedOntarioPre-EclampsiaPregnancyPremature BirthProportional Hazards ModelsRisk FactorsAutoimmune diseasescohort studiesfemalemothersOntariopregnancy complications

Identifiers

PMID39191479
PMCPMC11349189

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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 OpenQuestion graph.