Evidence map›Paper›PMID 39948598›Full record

ArticleBMC medicine2025

Life course trajectories of maternal cardiovascular disease risk factors by obstetric history: a UK cohort study using electronic health records.

Kate Birnie, Laura D Howe, Timothy Jones, Paul Madley-Dowd, Florence Z Martin, Harriet Forbes, Maria Theresa Redaniel, Rosie Cornish, Maria C Magnus, Neil M Davies and 4 more

Abstract read
In one paragraph

Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Observational
  2. Article
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

14 authors.

Kate BirnieMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK. kate.birnie@bristol.ac.uk.
Laura D HoweMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Timothy JonesBristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Paul Madley-DowdMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Florence Z MartinMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Harriet ForbesMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Maria Theresa RedanielBristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Rosie CornishMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Maria C MagnusCentre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.
Neil M DaviesDivision of Psychiatry, University College London, London, UK.
Kate TillingMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Alun D HughesMRC Unit for Lifelong Health and Ageing at University College London, London, UK.
Deborah A LawlorMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.
Abigail FraserMRC Integrative Epidemiology Unitat the , University of Bristol, Bristol, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWomen who experience adverse pregnancy outcomes (APOs; gestational hypertension, preeclampsia (PE), gestational diabetes (GD), preterm birth (PTB), small or large for gestational age, miscarriage, multiple miscarriages, stillbirth, and offspring with major congenital anomalies) have increased risk of developing cardiovascular disease (CVD). We aimed to compare cardiometabolic health trajectories across the life course between women with and without APOs.

methodsWe studied 187,186 women with a registered pregnancy in the UK Clinical Practice Research Datalink (CPRD) GOLD linked to Hospital Episode Statistics. Fractional polynomial multilevel models were used to compare trajectories of cardiometabolic risk factors (body mass index [BMI], blood pressure [BP], cholesterol, and glucose) between women with and without a history of APOs (individual APOs in any pregnancy and number of APOs). We explored two underlying time axes: (1) time relative to first pregnancy (from 10 years before first pregnancy to 15 years after) and (2) age. Models controlled for age at first pregnancy, residential area deprivation, non-singleton pregnancy, parity, smoking status, ethnicity, and medications use.

resultsWomen with a history of PE, gestational hypertension, or GD had higher BMI, BP, and glucose 10 years before first pregnancy compared to women without these APOs. These differences persisted 15 years post-first pregnancy. Women with a history of GD had a steeper post-partum rise in glucose. Women who experienced multiple (3 +) miscarriage, stillbirth, and/or medically indicated PTB had higher BP and BMI before and after pregnancy, with BP trajectories converging 15 years after first pregnancy. Women who experienced multiple APOs had the most adverse measurements across all cardiometabolic risk factors, with more unfavourable mean levels with each additional APO. There was little difference in cardiometabolic trajectories between women with and without a history of 1 or 2 miscarriages or congenital anomalies.

conclusionsWomen with APOs had adverse cardiometabolic profiles before first pregnancy, persisting up to 15 years post-pregnancy. Findings highlight the potential for targeted public health interventions to promote good cardiometabolic health in young adults transitioning from contraceptive use to planning pregnancies. APOs may identify young women who could benefit from monitoring CVD risk factors and interventions to improve cardiometabolic health.

Indexed as

Cardiovascular DiseasesHeart Disease Risk FactorsAdultBody Mass IndexCohort StudiesElectronic Health RecordsFemaleHumansPregnancyPregnancy OutcomeRisk FactorsUnited KingdomYoung AdultAdverse pregnancy outcomesCardiovascular risk factorsGestational diabetesGestational hypertensionPreeclampsia

Identifiers

PMID39948598
PMCPMC11827161

What Socratic holds

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Registered trials

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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.