Evidence map›Paper›PMID 35608601›Full record

ArticleCirculation. Genomic and precision medicine2022

Risk of Congenital Heart Defects in Offspring of Affected Mothers and Fathers.

Nina Øyen, Heather A Boyd, Lisbeth Carstensen, Lars Søndergaard, Jan Wohlfahrt, Mads Melbye

Open access · hybridAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Observational
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  15. Article
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  19. Mechanical heart valves and pregnancy.JRSM cardiovascular disease
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 3 countries.

Nina ØyenDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark (N.Ø., H.A.B., L.C., J.W.).ORCID 0000-0002-9807-1055
Heather A BoydDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark (N.Ø., H.A.B., L.C., J.W.).ORCID 0000-0001-6849-9985
Lisbeth CarstensenDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark (N.Ø., H.A.B., L.C., J.W.).ORCID 0000-0002-2425-633X
Lars SøndergaardDepartment of Cardiology (L.S.), University of Copenhagen, Denmark.
Jan WohlfahrtDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark (N.Ø., H.A.B., L.C., J.W.).ORCID 0000-0002-0019-2247
Mads MelbyeDepartment of Clinical Medicine (M.M.), University of Copenhagen, Denmark.ORCID 0000-0001-8264-6785
Statens Serum Institut · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmaller studies have reported a higher offspring risk of congenital heart defects (CHDs) for mothers with CHDs than for fathers with CHDs. In a large population-based study, we investigated whether offspring risk of CHD differed for mothers and fathers with CHDs.

methodsAll people born in Denmark, 1977 to 2011, with at least 1 registered parent, were included in our cohort (n=2 341 061). Parent-child recurrence of CHDs was evaluated using risk ratios (RRs) comparing risks of CHDs in individuals with and without a parent with a CHD, estimated using log-linear binomial regression.

resultsThe RRs for any CHD in offspring were 5.39 (95% CI, 4.88-5.96) for mothers and 3.04 (95% CI, 2.59-3.57) for fathers affected with any CHD; the ratio of RRs for mothers versus fathers was 1.82 (

conclusionsRecurrence risks of CHDs were significantly greater in the offspring of affected women than in the offspring of affected men. The excess maternal recurrence risks could not be explained by the slightly higher birth rates in women with CHDs.

Indexed as

Heart Defects, CongenitalHeart Septal DefectsCohort StudiesFathersFemaleHumansMaleRisk Factorsbirth ratecohort studiesepidemiologygeneticsheart defects, congenitalpopulationrisk

Identifiers

PMID35608601
PMCPMC9384828
OpenAlexW4281386616

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.