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BMJ 2005;331:877 (15 October), doi:10.1136/bmj.38555.462685.8F (published 16 September 2005)
Rolv Skjærven, professor1, Lars J Vatten, professor2, Allen J Wilcox3, Thorbjørn Rønning, statistician4, Lorentz M Irgens, professor5, Rolv Terje Lie, professor1
1 Section for Epidemiology and Medical Statistics, Department of Public Health and Primary Health Care, University of Bergen, Norway, 2 Norwegian University of Science and Technology, Faculty of Medicine, Trondheim, Norway, 3 National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA, 4 Division of Genes and Environment, Norwegian Institute of Public Health, Oslo, Norway, 5 Medical Birth Registry of Norway, Norwegian Institute of Public Health, Bergen, Norway
Correspondence to: R Skjærven Rolv.Skjaerven{at}smis.uib.no
Objectives To assess the impact on risk of pre-eclampsia of genes that work through the mother, and genes of paternal origin that work through the fetus.
Design Population based cohort study.
Setting Registry data from Norway.
Participants Linked generational data from the medical birth registry of Norway (1967-2003): 438 597 mother-offspring units and 286 945 father-offspring units.
Main outcome measures Pre-eclampsia in the second generation.
Results The daughters of women who had pre-eclampsia during pregnancy had more than twice the risk of pre-eclampsia themselves (odds ratio 2.2, 95% confidence interval 2.0 to 2.4) compared with other women. Men born after a pregnancy complicated by pre-eclampsia had a moderately increased risk of fathering a pre-eclamptic pregnancy (1.5, 1.3 to 1.7). Sisters of affected men or women, who were themselves born after pregnancies not complicated by pre-eclampsia, also had an increased risk (2.0, 1.7 to 2.3). Women and men born after pre-eclamptic pregnancies were more likely to trigger severe pre-eclampsia in their own (or their partner's) pregnancy (3.0, 2.4 to 3.7, for mothers and 1.9, 1.4 to 2.5, for fathers).
Conclusions Maternal genes and fetal genes from either the mother or father may trigger pre-eclampsia. The maternal association is stronger than the fetal association. The familial association predicts more severe pre-eclampsia.
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