Evidence map›Paper›PMID 40391426›Full record

ArticlePaediatric and perinatal epidemiology2025

Paternal Cardiometabolic Conditions and Perinatal Mortality.

Shwe Sin Win, Gerhard Sulo, Anders Engeland, Kari Klungsøyr

Abstract read
In one paragraph

Article in Paediatric and perinatal epidemiology, 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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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

4 authors.

Shwe Sin WinDepartment of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Bergen, Norway.ORCID https://orcid.org/0000-0003-4030-3826
Gerhard SuloDepartment of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Bergen, Norway.ORCID https://orcid.org/0000-0002-1247-1577
Anders EngelandDepartment of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Bergen, Norway.ORCID https://orcid.org/0000-0001-5620-9207
Kari KlungsøyrDepartment of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Bergen, Norway.ORCID https://orcid.org/0000-0003-2482-1690

Funding

The Dam foundation and the national association of unexpected child deaths
6 · The paper itself

Abstract

backgroundStudies have suggested that men with cardiometabolic conditions may have an increased risk of offspring perinatal mortality. However, this association remains underexplored.

objectivesWe aimed to study the association between fathers' cardiometabolic conditions and offspring perinatal mortality utilising linked data from national health registries in Norway.

methodsIn this population-based cohort study, males registered in the Medical Birth Registry of Norway (MBRN), born 1967-2005, were linked to their singleton offsprings born 2004-2020. The Norwegian Patient Registry and the Norwegian Prescription Database were used to define study exposures: history of hypertension, diabetes, dyslipidaemia, severe obesity or any of these at any time before/during the year of childbirth while fathers having no such conditions were the reference group. Perinatal mortality was defined as foetal death from 16 weeks' gestation or neonatal deaths within the first month after birth (from the MBRN). We fitted multilevel random-intercept Poisson regression models to account for the clustering of infants born to the same father. We reported incidence rate ratio (IRR) with 95% confidence Intervals (CI).

resultsOf 703,746 infants, 3.6% (n = 25,314) were born to fathers with any condition. Overall, 4827 (0.7%) of them died perinatally. In fully adjusted models, infants of fathers with hypertension had a 29% higher risk of dying perinatally (IRR 1.29, 95% CI 1.05, 1.57) relative to those of fathers without cardiometabolic conditions. Effect estimates for paternal diabetes, severe obesity and any condition also indicated a possible increased perinatal mortality associated with these conditions. In the sex-stratified analysis, the associations were stronger in male offspring (IRR 1.29, 95% CI 1.06, 1.58) than female offspring (IRR 1.01, 95% CI 0.78, 1.29).

conclusionsThe increased perinatal mortality in offspring to fathers with cardiometabolic conditions emphasises fathers' biological role in foetal and placental programming and development. Whether offspring sex impacts these associations needs further investigation.

Indexed as

FathersPerinatal MortalityAdultFemaleHumansInfant, NewbornMaleNorwayPregnancyRegistriesRisk Factorscardiometaboliclate miscarriagepaternal healthperinatal mortalitypreconceptionstillbirth

Identifiers

PMID40391426
PMCPMC12391856

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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.