dc.contributor.author | Sigmo, Gudrun David | |
dc.contributor.author | Hauge, Solveig | |
dc.contributor.author | Hufthammer, Karl Ove | |
dc.contributor.author | Wallenius, Marianne | |
dc.contributor.author | Salvesen, Kjell Åsmund Blix | |
dc.contributor.author | Daltveit, Anne Kjersti Nesje | |
dc.contributor.author | Bakland, Gunnstein | |
dc.contributor.author | Fevang, Bjørg Tilde Svanes | |
dc.date.accessioned | 2024-10-14T10:15:11Z | |
dc.date.available | 2024-10-14T10:15:11Z | |
dc.date.issued | 2024-03-12 | |
dc.description.abstract | Objectives To 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.<p>
<p>Methods This 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.
<p>Results The 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).
<p>Conclusion In 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. | en_US |
dc.identifier.citation | Sigmo, Hauge, Hufthammer, Wallenius, Salvesen, Daltveit, Bakland, Fevang. 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. Annals of the Rheumatic Diseases. 2024 | en_US |
dc.identifier.cristinID | FRIDAID 2248730 | |
dc.identifier.doi | 10.1136/ard-2023-224998 | |
dc.identifier.issn | 0003-4967 | |
dc.identifier.issn | 1468-2060 | |
dc.identifier.uri | https://hdl.handle.net/10037/35211 | |
dc.language.iso | eng | en_US |
dc.publisher | BMJ | en_US |
dc.relation.journal | Annals of the Rheumatic Diseases | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2024 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/4.0 | en_US |
dc.rights | Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) | en_US |
dc.title | 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 | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |