Obstetrical complications in patients with bipolar disorder and their siblings
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Cited by (58)
Gene-environment interactions in high-risk populations
2018, Bipolar Disorder Vulnerability: Perspectives from Pediatric and High-Risk PopulationsMaternal serum cytokine levels and risk of bipolar disorder
2017, Brain, Behavior, and ImmunityCitation Excerpt :Additionally, biospecimens were obtained and archived, including maternal serum samples from each trimester of pregnancy. Ascertainment of BD cases has been described in depth elsewhere (Canetta et al., 2014), and is summarized here. Cases with DSM-IV-TR BD, including bipolar I disorder, bipolar II disorder, BD not otherwise specified, and BD with psychotic features, were identified through the following 3 sources: the KPNC electronic medical records database, the Alameda County Behavioral Health Care Services (ACBHCS) database, and a mailing to the entire living CHDS birth cohort (mothers and children).
Neurodevelopmental origins of bipolar disorder: IPSC models
2016, Molecular and Cellular NeuroscienceCitation Excerpt :There have been reports of an association with advancing paternal age (Frans et al., 2008, Menezes et al., 2010); age having a stronger effect in early onset BP (Frans et al., 2008), and in schizophrenia (Ek et al., 2015), but the associations are minimal (1.37 fold). There are also reported associations with seasonality of birth (Torrey et al., 1997, Torrey, 1999), and with obstetric complications (Kinney et al., 1993,1998, Chudal et al., 2014), particularly with early onset BP (Guth et al., 1993). Prenatal exposure to drugs or birth complications were reported to increase risk of later diagnosis with BP by more than six-fold (Pavuluri et al., 2006), consistent with a meta-analysis that suggested a positive association between prenatal and perinatal complications with the development of BP in adult life (Buka and Fan, 1999).
Perinatal factors and the risk of bipolar disorder in Finland
2014, Journal of Affective DisordersCitation Excerpt :Complications during the perinatal period have been associated with psychiatric disorders like schizophrenia (Byrne et al., 2007; Abel et al., 2010; Cannon et al., 2002), autism (Kolevzon et al., 2007; Glasson et al., 2004) and affective disorders (Abel et al., 2010). However, studies on BPD have been inconsistent with some studies showing an increased risk in children exposed to perinatal complications (Kinney et al., 1993, 1998), while other studies failed to show similar associations (Verdoux and Bourgeois, 1993; Martelon et al., 2012). These complications include a variety of factors; some of the most noteworthy are indicators of fetal growth including birth weight, gestational age, and weight for gestational age (WGA), and what are often termed “obstetric complications,” including uterine bleeding, birth presentation, birth type, and Apgar score.
Bipolar and major depressive disorder: Neuroimaging the developmental-degenerative divide
2009, Neuroscience and Biobehavioral ReviewsNeurodevelopmental basis of bipolar disorder: A critical appraisal
2008, Progress in Neuro-Psychopharmacology and Biological Psychiatry
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Dennis K. Kinney, Ph.D., and Deborah L. Levy, Ph.D., are Associate Psychologists; Deborah A. Yurgelun-Todd, Ph.D., is Assistant Research Psychologist; and David Medoff, Clara M. Lajonchere, and Meg Radford-Paregol are research interns, Laboratories for Psychiatric Research, McLean Hospital, and Department of Psychiatry, Harvard Medical School.