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Using a Murine Model of Psychosocial Stress in Pregnancy as a Translationally Relevant Paradigm for Psychiatric Disorders in Mothers and Infants
Published on: June 13, 2021
Familial Risk of Postpartum Psychosis
Adrianna P Kępińska1, Thalia K Robakis1, Keith Humphreys1
1Seaver Autism Center for Research and Treatment (Kępińska, Mahjani), Department of Psychiatry (Kępińska, Robakis, Kahn, Bergink, Mahjani), Department of Genetics and Genomic Sciences (Kępińska, Mahjani), Mindich Child Health and Development Institute (Mahjani), and Department of Artificial Intelligence and Human Health (Mahjani), Icahn School of Medicine at Mount Sinai, New York; Department of Medical Epidemiology and Biostatistics (Humphreys, Mahjani) and Department of Molecular Medicine and Surgery (Mahjani), Karolinska Institutet, Stockholm; Department of Clinical Research, Research Unit Children and Adolescent Psychiatry, University of Southern Denmark, Odense (Liu, Munk-Olsen); Department of Psychiatry, Erasmus Medical Center, Rotterdam, the Netherlands (Bergink).
Objective:
Postpartum psychosis is one of the most severe psychiatric conditions, with high risks of suicide and infanticide if untreated. Although genetic factors contribute to the risk of postpartum psychosis, the extent of familial risk remains to be determined. The authors compared relative recurrence risk across different family relationship types, hypothesizing that relative recurrence risk for postpartum psychosis varies by degree of genetic relatedness and is higher in female full siblings than in cousins.
Methods:
This cohort study consisted of 1,648,759 women from the Swedish nationwide registers, of whom 2,514 (0.15%) experienced postpartum psychosis within 3 months of their first-ever childbirth. The authors estimated the relative recurrence risk of postpartum psychosis for female full siblings and cousins as a measure of familial risk.
Results:
The relative recurrence risk of postpartum psychosis in full siblings was 10.69 (95% CI=6.60, 16.26) when adjusted for year of and age at childbirth. Although cousins showed an elevated relative recurrence risk, these results did not reach statistical significance (1.78, 95% CI=0.70, 3.62). Despite the higher familial risk of postpartum psychosis among full siblings, the absolute risk for women with an affected sibling was relatively low, estimated at 1.60% within the entire population.
Conclusions:
The observed increased risk of postpartum psychosis in full siblings suggests both genetic and shared environmental influences. However, the lack of significant results in cousins hampers a more accurate distinction between these factors. Furthermore, despite increased relative recurrence risk in siblings, their overall likelihood of developing postpartum psychosis remains low. This study underscores the need for further research to better understand the intricate interplay of genetics and shared environment in the development of postpartum psychosis.
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