Cargando…

Elevated fetal steroidogenic activity in autism

Autism affects males more than females, giving rise to the idea that the influence of steroid hormones on early fetal brain development may be one important early biological risk factor. Utilizing the Danish Historic Birth Cohort and Danish Psychiatric Central Register, we identified all amniotic fl...

Descripción completa

Detalles Bibliográficos
Autores principales: Baron-Cohen, S, Auyeung, B, Nørgaard-Pedersen, B, Hougaard, D M, Abdallah, M W, Melgaard, L, Cohen, A S, Chakrabarti, B, Ruta, L, Lombardo, M V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184868/
https://www.ncbi.nlm.nih.gov/pubmed/24888361
http://dx.doi.org/10.1038/mp.2014.48
_version_ 1782337932441419776
author Baron-Cohen, S
Auyeung, B
Nørgaard-Pedersen, B
Hougaard, D M
Abdallah, M W
Melgaard, L
Cohen, A S
Chakrabarti, B
Ruta, L
Lombardo, M V
author_facet Baron-Cohen, S
Auyeung, B
Nørgaard-Pedersen, B
Hougaard, D M
Abdallah, M W
Melgaard, L
Cohen, A S
Chakrabarti, B
Ruta, L
Lombardo, M V
author_sort Baron-Cohen, S
collection PubMed
description Autism affects males more than females, giving rise to the idea that the influence of steroid hormones on early fetal brain development may be one important early biological risk factor. Utilizing the Danish Historic Birth Cohort and Danish Psychiatric Central Register, we identified all amniotic fluid samples of males born between 1993 and 1999 who later received ICD-10 (International Classification of Diseases, 10th Revision) diagnoses of autism, Asperger syndrome or PDD-NOS (pervasive developmental disorder not otherwise specified) (n=128) compared with matched typically developing controls. Concentration levels of Δ4 sex steroids (progesterone, 17α-hydroxy-progesterone, androstenedione and testosterone) and cortisol were measured with liquid chromatography tandem mass spectrometry. All hormones were positively associated with each other and principal component analysis confirmed that one generalized latent steroidogenic factor was driving much of the variation in the data. The autism group showed elevations across all hormones on this latent generalized steroidogenic factor (Cohen's d=0.37, P=0.0009) and this elevation was uniform across ICD-10 diagnostic label. These results provide the first direct evidence of elevated fetal steroidogenic activity in autism. Such elevations may be important as epigenetic fetal programming mechanisms and may interact with other important pathophysiological factors in autism.
format Online
Article
Text
id pubmed-4184868
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-41848682015-03-27 Elevated fetal steroidogenic activity in autism Baron-Cohen, S Auyeung, B Nørgaard-Pedersen, B Hougaard, D M Abdallah, M W Melgaard, L Cohen, A S Chakrabarti, B Ruta, L Lombardo, M V Mol Psychiatry Original Article Autism affects males more than females, giving rise to the idea that the influence of steroid hormones on early fetal brain development may be one important early biological risk factor. Utilizing the Danish Historic Birth Cohort and Danish Psychiatric Central Register, we identified all amniotic fluid samples of males born between 1993 and 1999 who later received ICD-10 (International Classification of Diseases, 10th Revision) diagnoses of autism, Asperger syndrome or PDD-NOS (pervasive developmental disorder not otherwise specified) (n=128) compared with matched typically developing controls. Concentration levels of Δ4 sex steroids (progesterone, 17α-hydroxy-progesterone, androstenedione and testosterone) and cortisol were measured with liquid chromatography tandem mass spectrometry. All hormones were positively associated with each other and principal component analysis confirmed that one generalized latent steroidogenic factor was driving much of the variation in the data. The autism group showed elevations across all hormones on this latent generalized steroidogenic factor (Cohen's d=0.37, P=0.0009) and this elevation was uniform across ICD-10 diagnostic label. These results provide the first direct evidence of elevated fetal steroidogenic activity in autism. Such elevations may be important as epigenetic fetal programming mechanisms and may interact with other important pathophysiological factors in autism. Nature Publishing Group 2015-03 2014-06-03 /pmc/articles/PMC4184868/ /pubmed/24888361 http://dx.doi.org/10.1038/mp.2014.48 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Original Article
Baron-Cohen, S
Auyeung, B
Nørgaard-Pedersen, B
Hougaard, D M
Abdallah, M W
Melgaard, L
Cohen, A S
Chakrabarti, B
Ruta, L
Lombardo, M V
Elevated fetal steroidogenic activity in autism
title Elevated fetal steroidogenic activity in autism
title_full Elevated fetal steroidogenic activity in autism
title_fullStr Elevated fetal steroidogenic activity in autism
title_full_unstemmed Elevated fetal steroidogenic activity in autism
title_short Elevated fetal steroidogenic activity in autism
title_sort elevated fetal steroidogenic activity in autism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184868/
https://www.ncbi.nlm.nih.gov/pubmed/24888361
http://dx.doi.org/10.1038/mp.2014.48
work_keys_str_mv AT baroncohens elevatedfetalsteroidogenicactivityinautism
AT auyeungb elevatedfetalsteroidogenicactivityinautism
AT nørgaardpedersenb elevatedfetalsteroidogenicactivityinautism
AT hougaarddm elevatedfetalsteroidogenicactivityinautism
AT abdallahmw elevatedfetalsteroidogenicactivityinautism
AT melgaardl elevatedfetalsteroidogenicactivityinautism
AT cohenas elevatedfetalsteroidogenicactivityinautism
AT chakrabartib elevatedfetalsteroidogenicactivityinautism
AT rutal elevatedfetalsteroidogenicactivityinautism
AT lombardomv elevatedfetalsteroidogenicactivityinautism