Evidence map›Paper›PMID 38262688›Full record

ArticleAnnals of the rheumatic diseases2024

Male patients with inflammatory joint diseases are less likely than controls to be childless: results from a Norwegian population-based cohort study of 10 865 patients.

Gudrun David Sigmo, Solveig Hauge, Karl Ove Hufthammer, Marianne Wallenius, Kjell Åsmund Salvesen, Anne Kjersti Nesje Daltveit, Gunnstein Bakland, Bjorg-Tilde Svanes Fevang

Open access · hybridAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 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
2.7field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Gudrun David SigmoDepartment of Rheumatology, Stavanger University Hospital, Stavanger, Norway gudrun.david.sigmo@sus.no.ORCID http://orcid.org/0009-0009-1851-0723
Solveig HaugeDepartment of Rheumatology, Haukeland University Hospital, Bergen, Norway.
Karl Ove HufthammerCentre for Clinical Research, Haukeland University Hospital, Bergen, Norway.ORCID http://orcid.org/0000-0003-3170-9496
Marianne WalleniusDepartment of Neuroscience, Norwegian University of Science and Technology, Trondheim, Norway.
Kjell Åsmund SalvesenDepartment of Obstetrics and Gynecology, St Olavs Hospital Trondheim University Hospital, Trondheim, Norway.
Anne Kjersti Nesje DaltveitDepartment of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Gunnstein BaklandDepartment of Rheumatology, University Hospital of Northern Norway, Tromsø, Norway.
Bjorg-Tilde Svanes FevangDepartment of Rheumatology, Haukeland University Hospital, Bergen, Norway.
Haukeland University Hospital · NONorwegian University of Science and Technology · NONorwegian Institute of Public Health · NOStavanger University Hospital · NOUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the number of children per man and the proportion of childless men as a proxy of fertility in a national cohort of men with inflammatory joint diseases (IJDs), compared with matched controls from the general population.

methodsThis is a nationwide, population-based retrospective cohort study. Male patients with IJDs (n = 10 865) in the Norwegian Arthritis Registry were individually matched 1:5 on birth year and county of residence with men without IJDs obtained from the National Population Register (n = 54 325). Birth data were obtained from the Medical Birth Registry of Norway. We compared the mean number of children per man and the proportion of childless men and analysed the impact of age and year of diagnosis.

resultsThe mean number of children per man in the patient group was 1.80 versus 1.69 in the comparison group (p <0.001), and 21% of the patients in the patient group were childless versus 27% in the comparison group (p <0.001). The finding of less childlessness and higher number of children per man remained consistent across age at diagnosis, except for those diagnosed at age 0-19 years. The difference in childlessness was most pronounced for men diagnosed after year 2000, especially when diagnosed at 30-39 years of age (22% vs 32%, p<0.001).

conclusionIn this large cohort study we found that patients with IJD have a higher number of children and are less likely to be childless compared with controls. Factors associated with developing or having an IJD might influence fertility and this requires further investigation.

Indexed as

ArthritisAdolescentAdultChildChild, PreschoolCohort StudiesHumansInfantInfant, NewbornMaleNorwayRetrospective StudiesYoung AdultArthritisArthritis, PsoriaticArthritis, RheumatoidEpidemiologySpondylitis, Ankylosing

Identifiers

PMID38262688
PMCPMC10958328
OpenAlexW4391136621

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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 OpenQuestion graph.