Key result
Paternal family history of coronary heart disease was not associated with perinatal death (1.3% vs 1.3%; OR 1.00, 95% CI 0.92-1.08), with similar null findings for family history of stroke.
Why the study?
While pregnancies conceived by fathers with modifiable cardiovascular risk factors have a higher risk of loss, the association between paternal family history of premature atherosclerotic disease and perinatal death remained unknown.
Does paternal family history of premature atherosclerotic disease increase the risk of perinatal death in singleton births?
Cohort (n=512,111)
Does paternal family history of premature atherosclerotic disease increase the risk of perinatal death in singleton births?
Paternal family history of premature atherosclerotic disease is not associated with an increased risk of perinatal death, stillbirth, or neonatal death.
Paternal family history may signal perinatal risk; hypothesis-generating and requires prospective validation before any clinical consideration.
BACKGROUND: Studies have reported that pregnancies conceived by fathers with modifiable cardiovascular risk factors are at higher risk of ending in losses compared to those without such risk factors. Our objective was to examine the association between paternal family history _a non-modifiable risk factor_ of premature atherosclerotic disease and perinatal death. METHODS: This is a population-based cohort study. Information on fathers, aged 18-50 years who participated in three population-based health surveys conducted in Norway during 1974-2003 was linked to their singleton births registered in the Medical Birth Registry of Norway. We used multilevel mixed effect logistic regression analyses with random intercepts by father's identification number. The birth was the observation unit in all analyses. RESULTS: A total of 220,386 fathers who had 512,111 births with information on family history of CHD (12.3% with positive family history) and 203,257 births with information on family history of stroke (9.2% with positive family history) were analysed. There were 782 (1.3%) and 195 (1%) perinatal deaths in births to fathers with family history of CHD and stroke while 5,922 (1.3%) and 1,858 (1%) in those without family histories. We found no association between family history of CHD and stillbirth (OR 1.01, 95% CI 0.92; 1.12), neonatal death (OR 0.98, 95%CI 0.86, 1.11) or perinatal death (OR 1.00, 95% CI 0.92, 1.08). Similarly, we found no associations between family history of stroke and stillbirth (OR 1.00, 95% CI 0.82, 1.21), neonatal death (OR 1.09, 95%CI 0.84, 1.41) or perinatal death (OR 1.02, 95% CI 0.88, 1.20). LIMITATIONS: Socioeconomic background of fathers was captured using imperfect proxy. Potential misclassification of family history and selection bias should be considered. CONCLUSION: Results of this large, cohort study including half-a million births, do not indicate an association between paternal family history of premature atherosclerotic disease and perinatal death.
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Win et al. (2025) conducted a cohort in Perinatal death (n=512,111). Paternal family history of premature atherosclerotic disease vs. No paternal family history of premature atherosclerotic disease was evaluated on Perinatal death (OR 1.00, 95% CI 0.92, 1.08). Paternal family history of coronary heart disease was not associated with perinatal death (1.3% vs 1.3%; OR 1.00, 95% CI 0.92-1.08), with similar null findings for family history of stroke.
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