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Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory

Elevated levels of prenatal testosterone may increase the risk for autism spectrum conditions (autism). Given that polycystic ovary syndrome (PCOS) is also associated with elevated prenatal testosterone and its precursor sex steroids, a hypothesis from the prenatal sex steroid theory is that women w...

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Autores principales: Cherskov, Adriana, Pohl, Alexa, Allison, Carrie, Zhang, Heping, Payne, Rupert A., Baron-Cohen, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068102/
https://www.ncbi.nlm.nih.gov/pubmed/30065244
http://dx.doi.org/10.1038/s41398-018-0186-7
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author Cherskov, Adriana
Pohl, Alexa
Allison, Carrie
Zhang, Heping
Payne, Rupert A.
Baron-Cohen, Simon
author_facet Cherskov, Adriana
Pohl, Alexa
Allison, Carrie
Zhang, Heping
Payne, Rupert A.
Baron-Cohen, Simon
author_sort Cherskov, Adriana
collection PubMed
description Elevated levels of prenatal testosterone may increase the risk for autism spectrum conditions (autism). Given that polycystic ovary syndrome (PCOS) is also associated with elevated prenatal testosterone and its precursor sex steroids, a hypothesis from the prenatal sex steroid theory is that women with PCOS should have elevated autistic traits and a higher rate of autism among their children. Using electronic health records obtained from the Clinical Practice Research Datalink (CPRD) in the UK between 1990 and 2014, we conducted three matched case-control studies. Studies 1 and 2 examined the risk of PCOS in women with autism (n = 971) and the risk of autism in women with PCOS (n = 26,263), respectively, compared with matched controls. Study 3 examined the odds ratio (OR) of autism in first-born children of women with PCOS (n = 8588), matched to 41,127 controls. In Studies 1 and 2 we found increased prevalence of PCOS in women with autism (2.3% vs. 1.1%; unadjusted OR: 2.01, 95% CI: 1.22–3.30) and elevated rates of autism in women with PCOS (0.17% vs. 0.09%, unadjusted OR: 1.94 CI: 1.37–2.76). In Study 3 we found the odds of having a child with autism were significantly increased, even after adjustment for maternal psychiatric diagnoses, obstetric complications, and maternal metabolic conditions (unadjusted OR: 1.60, 95% CI: 1.28–2.00; adjusted OR: 1.35, 95% CI: 1.06–1.73). These studies provide further evidence that women with PCOS and their children have a greater risk of autism.
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spelling pubmed-60681022018-08-01 Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory Cherskov, Adriana Pohl, Alexa Allison, Carrie Zhang, Heping Payne, Rupert A. Baron-Cohen, Simon Transl Psychiatry Article Elevated levels of prenatal testosterone may increase the risk for autism spectrum conditions (autism). Given that polycystic ovary syndrome (PCOS) is also associated with elevated prenatal testosterone and its precursor sex steroids, a hypothesis from the prenatal sex steroid theory is that women with PCOS should have elevated autistic traits and a higher rate of autism among their children. Using electronic health records obtained from the Clinical Practice Research Datalink (CPRD) in the UK between 1990 and 2014, we conducted three matched case-control studies. Studies 1 and 2 examined the risk of PCOS in women with autism (n = 971) and the risk of autism in women with PCOS (n = 26,263), respectively, compared with matched controls. Study 3 examined the odds ratio (OR) of autism in first-born children of women with PCOS (n = 8588), matched to 41,127 controls. In Studies 1 and 2 we found increased prevalence of PCOS in women with autism (2.3% vs. 1.1%; unadjusted OR: 2.01, 95% CI: 1.22–3.30) and elevated rates of autism in women with PCOS (0.17% vs. 0.09%, unadjusted OR: 1.94 CI: 1.37–2.76). In Study 3 we found the odds of having a child with autism were significantly increased, even after adjustment for maternal psychiatric diagnoses, obstetric complications, and maternal metabolic conditions (unadjusted OR: 1.60, 95% CI: 1.28–2.00; adjusted OR: 1.35, 95% CI: 1.06–1.73). These studies provide further evidence that women with PCOS and their children have a greater risk of autism. Nature Publishing Group UK 2018-08-01 /pmc/articles/PMC6068102/ /pubmed/30065244 http://dx.doi.org/10.1038/s41398-018-0186-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cherskov, Adriana
Pohl, Alexa
Allison, Carrie
Zhang, Heping
Payne, Rupert A.
Baron-Cohen, Simon
Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title_full Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title_fullStr Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title_full_unstemmed Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title_short Polycystic ovary syndrome and autism: A test of the prenatal sex steroid theory
title_sort polycystic ovary syndrome and autism: a test of the prenatal sex steroid theory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068102/
https://www.ncbi.nlm.nih.gov/pubmed/30065244
http://dx.doi.org/10.1038/s41398-018-0186-7
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