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Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder

BACKGROUND: Pre- and perinatal adversities may increase the risk for schizophrenia and bipolar disorder. Hypoxia-related obstetric complications (OCs) are associated with brain anatomical abnormalities in schizophrenia, but their association with brain anatomy variation in bipolar disorder is unknow...

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Autores principales: Haukvik, U. K., McNeil, T., Lange, E. H., Melle, I., Dale, A. M., Andreassen, O. A., Agartz, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936825/
https://www.ncbi.nlm.nih.gov/pubmed/23803260
http://dx.doi.org/10.1017/S0033291713001529
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author Haukvik, U. K.
McNeil, T.
Lange, E. H.
Melle, I.
Dale, A. M.
Andreassen, O. A.
Agartz, I.
author_facet Haukvik, U. K.
McNeil, T.
Lange, E. H.
Melle, I.
Dale, A. M.
Andreassen, O. A.
Agartz, I.
author_sort Haukvik, U. K.
collection PubMed
description BACKGROUND: Pre- and perinatal adversities may increase the risk for schizophrenia and bipolar disorder. Hypoxia-related obstetric complications (OCs) are associated with brain anatomical abnormalities in schizophrenia, but their association with brain anatomy variation in bipolar disorder is unknown. METHOD: Magnetic resonance imaging brain scans, clinical examinations and data from the Medical Birth Registry of Norway were obtained for 219 adults, including 79 patients with a DSM-IV diagnosis of bipolar disorder (age 29.4 years, s.d. = 11.8 years, 39% male) and 140 healthy controls (age 30.8 years, s.d. = 12.0 years, 53% male). Severe hypoxia-related OCs throughout pregnancy/birth and perinatal asphyxia were each studied in relation to a priori selected brain volumes (hippocampus, lateral ventricles and amygdala, obtained with FreeSurfer), using linear regression models covarying for age, sex, medication use and intracranial volume. Multiple comparison adjustment was applied. RESULTS: Perinatal asphyxia was associated with smaller left amygdala volume (t = −2.59, p = 0.012) in bipolar disorder patients, but not in healthy controls. Patients with psychotic bipolar disorder showed distinct associations between perinatal asphyxia and smaller left amygdala volume (t = −2.69, p = 0.010), whereas patients with non-psychotic bipolar disorder showed smaller right hippocampal volumes related to both perinatal asphyxia (t = −2.60, p = 0.015) and severe OCs (t = −3.25, p = 0.003). No associations between asphyxia or severe OCs and the lateral ventricles were found. CONCLUSIONS: Pre- and perinatal hypoxia-related OCs are related to brain morphometry in bipolar disorder in adulthood, with specific patterns in patients with psychotic versus non-psychotic illness.
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spelling pubmed-39368252014-02-28 Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder Haukvik, U. K. McNeil, T. Lange, E. H. Melle, I. Dale, A. M. Andreassen, O. A. Agartz, I. Psychol Med Original Articles BACKGROUND: Pre- and perinatal adversities may increase the risk for schizophrenia and bipolar disorder. Hypoxia-related obstetric complications (OCs) are associated with brain anatomical abnormalities in schizophrenia, but their association with brain anatomy variation in bipolar disorder is unknown. METHOD: Magnetic resonance imaging brain scans, clinical examinations and data from the Medical Birth Registry of Norway were obtained for 219 adults, including 79 patients with a DSM-IV diagnosis of bipolar disorder (age 29.4 years, s.d. = 11.8 years, 39% male) and 140 healthy controls (age 30.8 years, s.d. = 12.0 years, 53% male). Severe hypoxia-related OCs throughout pregnancy/birth and perinatal asphyxia were each studied in relation to a priori selected brain volumes (hippocampus, lateral ventricles and amygdala, obtained with FreeSurfer), using linear regression models covarying for age, sex, medication use and intracranial volume. Multiple comparison adjustment was applied. RESULTS: Perinatal asphyxia was associated with smaller left amygdala volume (t = −2.59, p = 0.012) in bipolar disorder patients, but not in healthy controls. Patients with psychotic bipolar disorder showed distinct associations between perinatal asphyxia and smaller left amygdala volume (t = −2.69, p = 0.010), whereas patients with non-psychotic bipolar disorder showed smaller right hippocampal volumes related to both perinatal asphyxia (t = −2.60, p = 0.015) and severe OCs (t = −3.25, p = 0.003). No associations between asphyxia or severe OCs and the lateral ventricles were found. CONCLUSIONS: Pre- and perinatal hypoxia-related OCs are related to brain morphometry in bipolar disorder in adulthood, with specific patterns in patients with psychotic versus non-psychotic illness. Cambridge University Press 2014-04 2013-06-27 /pmc/articles/PMC3936825/ /pubmed/23803260 http://dx.doi.org/10.1017/S0033291713001529 Text en © Cambridge University Press 2013 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution licence <http://creativecommons.org/licenses/by/3.0/.
spellingShingle Original Articles
Haukvik, U. K.
McNeil, T.
Lange, E. H.
Melle, I.
Dale, A. M.
Andreassen, O. A.
Agartz, I.
Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title_full Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title_fullStr Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title_full_unstemmed Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title_short Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
title_sort pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936825/
https://www.ncbi.nlm.nih.gov/pubmed/23803260
http://dx.doi.org/10.1017/S0033291713001529
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