Evidence map›Paper›PMID 40610749›Full record

ArticleBJC reports2025

Cancer risk after preeclampsia: a cohort study in two Nordic populations.

Golbarg Vesterlund, Xinhe Mao, Mika Gissler, Manuchehr Abedi-Valugerdi, Tiina Skoog, Seppo Heinonen, Pär Sparen, Karin Pettersson, Juha Kere, Kamila Czene and 1 more

Abstract read
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Article in BJC reports, 2025. 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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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Golbarg VesterlundDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden. golbarg.vesterlund@ki.se.ORCID http://orcid.org/0009-0000-8946-5047
Xinhe MaoDepartment of Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Mika GisslerDepartment of Data and Analytics, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
Manuchehr Abedi-ValugerdiDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Tiina SkoogDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Seppo HeinonenDepartment of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Pär SparenDepartment of Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Karin PetterssonDepartment of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Juha KereDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Kamila CzeneDepartment of Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Satu WedenojaDepartment of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLimited evidence suggests that preeclampsia (PE) is associated with reduced cancer risk later in life. We aimed to investigate this using large registry-based cohorts. We hypothesised that enhanced immune activation in PE women, suggested by autoimmune-type reactivity, lowers their subsequent cancer risk.

methodsUtilising Medical Birth Registry data from Sweden and Finland, we identified 123,495 women with PE and 3,223,537 women without. Data were cross-linked to the national Cancer Registries. Incidence rate ratios with 95% CIs were calculated and adjusted for maternal birth year, age at first birth, and parity.

resultsOverall cancer risk was significantly lower in Swedish PE women (IRR 0.91) but not in Finnish. Lower IRRs in PE women were found in both cohorts for breast (IRR 0.90 and 0.91), cervical (IRR 0.79 and 0.55) and lung cancer (IRR 0.72 and 0.63), while endometrial cancer showed increased incidence (IRR 1.28 and 1.46). Foetal sex had no impact on cancer risk. Among Swedish siblings to PE women, a slight reduction in cancer risk, driven by lower lung cancer incidence (IRR 0.86), was noted.

conclusionOur data show a link between PE and subsequent cancer risk, suggesting that shared mechanisms may predispose to PE and influence cancer development.

Identifiers

PMID40610749
PMCPMC12229669

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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.