Perinatal complications in unaffected sisters of anorexia nervosa patients: testing a covariation model between genetic and environmental factors
- PMID: 21193995
- DOI: 10.1007/s00406-010-0181-3
Perinatal complications in unaffected sisters of anorexia nervosa patients: testing a covariation model between genetic and environmental factors
Abstract
Although perinatal complications are hypothesized to be risk factors for the development of anorexia nervosa (AN), no study to date explored this issue using a discordant sibling design. This type of design allows to explore whether the risk for obstetric complications is itself a consequence of the genetic vulnerability for AN (covariation model) or whether obstetric complications increase the risk of AN independently of (additive model), or in interaction with (interaction model), the disorder's genetic liability. The presence of perinatal complications was assessed through review of the obstetric records of 60 AN subjects, 60 unaffected sisters, and 70 healthy subjects. Unaffected sisters and healthy controls were compared in relation to perinatal characteristics and complications. There was no evidence for an elevated rate of complications in unaffected siblings of AN patients. Mothers with a positive psychiatric history tended to have more perinatal complications. Perinatal complications seem to be independent risk factors that may interact with, but are not caused by, familial risk factors for AN. In terms of prevention, a particular attention should be paid to mothers with a lifetime history of psychiatric disorders.
Similar articles
-
Perinatal factors and the risk of developing anorexia nervosa and bulimia nervosa.Arch Gen Psychiatry. 2006 Jan;63(1):82-8. doi: 10.1001/archpsyc.63.1.82. Arch Gen Psychiatry. 2006. PMID: 16389201
-
The relationship between obstetric complications and temperament in eating disorders: a mediation hypothesis.Psychosom Med. 2008 Apr;70(3):372-7. doi: 10.1097/PSY.0b013e318164604e. Epub 2008 Feb 6. Psychosom Med. 2008. PMID: 18256341
-
Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings.JAMA Psychiatry. 2013 Jan;70(1):22-30. doi: 10.1001/jamapsychiatry.2013.268. JAMA Psychiatry. 2013. PMID: 23147713
-
Anorexia nervosa: definition, epidemiology, and cycle of risk.Int J Eat Disord. 2005;37 Suppl:S2-9; discussion S20-1. doi: 10.1002/eat.20107. Int J Eat Disord. 2005. PMID: 15852310 Review.
-
Prenatal and perinatal risk factors of schizophrenia.J Matern Fetal Neonatal Med. 2012 Dec;25(12):2559-63. doi: 10.3109/14767058.2012.699118. Epub 2012 Jul 18. J Matern Fetal Neonatal Med. 2012. PMID: 22646662 Review.
Cited by
-
Catechol-O-methyltransferase genotype modifies executive functioning and prefrontal functional connectivity in women with anorexia nervosa.J Psychiatry Neurosci. 2013 Jul;38(4):241-8. doi: 10.1503/jpn.120068. J Psychiatry Neurosci. 2013. PMID: 23046831 Free PMC article.
-
Eating Disorders, Pregnancy, and the Postpartum Period: Findings from the Norwegian Mother and Child Cohort Study (MoBa).Nor Epidemiol. 2014 Jan 1;24(1-2):51-62. doi: 10.5324/nje.v24i1-2.1758. Nor Epidemiol. 2014. PMID: 27110061 Free PMC article.
-
Recent Advances in Developmental and Risk Factor Research on Eating Disorders.Curr Psychiatry Rep. 2015 Jun;17(6):42. doi: 10.1007/s11920-015-0585-x. Curr Psychiatry Rep. 2015. PMID: 25894358 Review.
-
Achievement and maintenance of the new impact factor 2010.Eur Arch Psychiatry Clin Neurosci. 2011 Sep;261(6):387-9. doi: 10.1007/s00406-011-0237-z. Eur Arch Psychiatry Clin Neurosci. 2011. PMID: 21861244 Free PMC article. No abstract available.
References
MeSH terms
LinkOut - more resources
Full Text Sources
Medical