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BMJ. 2010 Apr 29;340:c2050. doi: 10.1136/bmj.c2050.

Recurrence of hyperemesis gravidarum across generations: population based cohort study.

Author information

1
Division of Epidemiology, Norwegian Institute of Public Health, PO Box 4404, Nydalen, N-0403 Oslo, Norway. ase.vigdis.vikanes@fhi.no

Abstract

OBJECTIVE:

To estimate the risk of hyperemesis gravidarum (hyperemesis) according to whether the daughters and sons under study were born after pregnancies complicated by hyperemesis.

DESIGN:

Population based cohort study.

SETTING:

Registry data from Norway.

PARTICIPANTS:

Linked generational data from the medical birth registry of Norway (1967-2006): 544 087 units of mother and childbearing daughter and 399 777 units of mother and child producing son.

MAIN OUTCOME MEASURE:

Hyperemesis in daughters in mother and childbearing daughter units and hyperemesis in female partners of sons in mother and child producing son units.

RESULTS:

Daughters who were born after a pregnancy complicated by hyperemesis had a 3% risk of having hyperemesis in their own pregnancy, while women who were born after an unaffected pregnancy had a risk of 1.1% (unadjusted odds ratio 2.9, 95% confidence interval 2.4 to 3.6). Female partners of sons who were born after pregnancies complicated by hyperemesis had a risk of 1.2% (1.0, 0.7 to 1.6). Daughters born after a pregnancy not complicated by hyperemesis had an increased risk of the condition if the mother had hyperemesis in a previous or subsequent pregnancy (3.2 (1.6 to 6.4) if hyperemesis had occurred in one of the mother's previous pregnancies and 3.7 (1.5 to 9.1) if it had occurred in a later pregnancy). Adjustment for maternal age at childbirth, period of birth, and parity did not change the estimates. Restrictions to firstborns did not influence the results.

CONCLUSIONS:

Hyperemesis gravidarum is more strongly influenced by the maternal genotype than the fetal genotype, though environmental influences along the maternal line cannot be excluded as contributing factors.

PMID:
21030362
PMCID:
PMC2862151
DOI:
10.1136/bmj.c2050
[Indexed for MEDLINE]
Free PMC Article

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