Sigmo Gudrun David, Hauge Solveig, Hufthammer Karl Ove, Wallenius Marianne, Salvesen Kjell Åsmund, Daltveit Anne Kjersti Nesje, Bakland Gunnstein, Fevang Bjorg-Tilde Svanes
Department of Rheumatology, Stavanger University Hospital, Stavanger, Norway
Department of Rheumatology, Haukeland University Hospital, Bergen, Norway.
Ann Rheum Dis. 2024 Mar 12;83(4):457-463. doi: 10.1136/ard-2023-224998.
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.
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.
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).
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.
在一个全国性的炎性关节病(IJD)男性队列中,调查每名男性的子女数量以及无子女男性的比例,以此作为生育能力的指标,并与来自普通人群的匹配对照进行比较。
这是一项基于全国人口的回顾性队列研究。挪威关节炎登记处的IJD男性患者(n = 10865),根据出生年份和居住县,与从国家人口登记处获取的无IJD男性(n = 54325)进行1:5个体匹配。出生数据来自挪威医疗出生登记处。我们比较了每名男性的平均子女数量和无子女男性的比例,并分析了年龄和诊断年份的影响。
患者组中每名男性的平均子女数量为1.80,而对照组为1.69(p < 0.001);患者组中21%的患者无子女,而对照组为27%(p < 0.001)。除0至19岁诊断的患者外,在各诊断年龄组中,无子女情况较少且每名男性子女数量较多这一发现保持一致。2000年后诊断的男性,无子女差异最为明显,尤其是30至39岁诊断的男性(22%对32%,p < 0.001)。
在这项大型队列研究中,我们发现与对照组相比,IJD患者的子女数量更多且无子女的可能性更小。与IJD发生或患病相关的因素可能会影响生育能力,这需要进一步研究。