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Sex differences in placenta-derived markers and later autistic traits in children

Autism is more prevalent in males and males on average score higher on measures of autistic traits. Placental function is affected significantly by the sex of the fetus. It is unclear if sex differences in placental function are associated with sex differences in the occurrence of autistic traits po...

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Autores principales: Tsompanidis, A., Blanken, L., Broere-Brown, Z. A., van Rijn, B. B., Baron-Cohen, S., Tiemeier, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344956/
https://www.ncbi.nlm.nih.gov/pubmed/37443170
http://dx.doi.org/10.1038/s41398-023-02552-w
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author Tsompanidis, A.
Blanken, L.
Broere-Brown, Z. A.
van Rijn, B. B.
Baron-Cohen, S.
Tiemeier, H.
author_facet Tsompanidis, A.
Blanken, L.
Broere-Brown, Z. A.
van Rijn, B. B.
Baron-Cohen, S.
Tiemeier, H.
author_sort Tsompanidis, A.
collection PubMed
description Autism is more prevalent in males and males on average score higher on measures of autistic traits. Placental function is affected significantly by the sex of the fetus. It is unclear if sex differences in placental function are associated with sex differences in the occurrence of autistic traits postnatally. To assess this, concentrations of angiogenesis-related markers, placental growth factor (PlGF) and soluble fms-like tyrosine kinase (sFlt-1) were assessed in maternal plasma of expectant women in the late 1(st) (mean= 13.5 [SD = 2.0] weeks gestation) and 2(nd) trimesters (mean=20.6 [SD = 1.2] weeks gestation), as part of the Generation R Study, Rotterdam, the Netherlands. Subsequent assessment of autistic traits in the offspring at age 6 was performed with the 18-item version of the Social Responsiveness Scale (SRS). Associations of placental protein concentrations with autistic traits were tested in sex-stratified and cohort-wide regression models. Cases with pregnancy complications or a later autism diagnosis (n = 64) were also assessed for differences in placenta-derived markers. sFlt-1 levels were significantly lower in males in both trimesters but showed no association with autistic traits. PlGF was significantly lower in male pregnancies in the 1(st) trimester, and significantly higher in the 2(nd) trimester, compared to female pregnancies. Higher PlGF levels in the 2(nd) trimester and the rate of PlGF increase were both associated with the occurrence of higher autistic traits (PlGF-2(nd): n = 3469,b = 0.24 [SE = 0.11], p = 0.03) in both unadjusted and adjusted linear regression models that controlled for age, sex, placental weight and maternal characteristics. Mediation analyses showed that higher autistic traits in males compared to females were partly explained by higher PlGF or a faster rate of PlGF increase in the second trimester (PlGF-2(nd): n = 3469, ACME: b = 0.005, [SE = 0.002], p = 0.004). In conclusion, higher PlGF levels in the 2(nd) trimester and a higher rate of PlGF increase are associated with both being male, and with a higher number of autistic traits in the general population.
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spelling pubmed-103449562023-07-15 Sex differences in placenta-derived markers and later autistic traits in children Tsompanidis, A. Blanken, L. Broere-Brown, Z. A. van Rijn, B. B. Baron-Cohen, S. Tiemeier, H. Transl Psychiatry Article Autism is more prevalent in males and males on average score higher on measures of autistic traits. Placental function is affected significantly by the sex of the fetus. It is unclear if sex differences in placental function are associated with sex differences in the occurrence of autistic traits postnatally. To assess this, concentrations of angiogenesis-related markers, placental growth factor (PlGF) and soluble fms-like tyrosine kinase (sFlt-1) were assessed in maternal plasma of expectant women in the late 1(st) (mean= 13.5 [SD = 2.0] weeks gestation) and 2(nd) trimesters (mean=20.6 [SD = 1.2] weeks gestation), as part of the Generation R Study, Rotterdam, the Netherlands. Subsequent assessment of autistic traits in the offspring at age 6 was performed with the 18-item version of the Social Responsiveness Scale (SRS). Associations of placental protein concentrations with autistic traits were tested in sex-stratified and cohort-wide regression models. Cases with pregnancy complications or a later autism diagnosis (n = 64) were also assessed for differences in placenta-derived markers. sFlt-1 levels were significantly lower in males in both trimesters but showed no association with autistic traits. PlGF was significantly lower in male pregnancies in the 1(st) trimester, and significantly higher in the 2(nd) trimester, compared to female pregnancies. Higher PlGF levels in the 2(nd) trimester and the rate of PlGF increase were both associated with the occurrence of higher autistic traits (PlGF-2(nd): n = 3469,b = 0.24 [SE = 0.11], p = 0.03) in both unadjusted and adjusted linear regression models that controlled for age, sex, placental weight and maternal characteristics. Mediation analyses showed that higher autistic traits in males compared to females were partly explained by higher PlGF or a faster rate of PlGF increase in the second trimester (PlGF-2(nd): n = 3469, ACME: b = 0.005, [SE = 0.002], p = 0.004). In conclusion, higher PlGF levels in the 2(nd) trimester and a higher rate of PlGF increase are associated with both being male, and with a higher number of autistic traits in the general population. Nature Publishing Group UK 2023-07-13 /pmc/articles/PMC10344956/ /pubmed/37443170 http://dx.doi.org/10.1038/s41398-023-02552-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tsompanidis, A.
Blanken, L.
Broere-Brown, Z. A.
van Rijn, B. B.
Baron-Cohen, S.
Tiemeier, H.
Sex differences in placenta-derived markers and later autistic traits in children
title Sex differences in placenta-derived markers and later autistic traits in children
title_full Sex differences in placenta-derived markers and later autistic traits in children
title_fullStr Sex differences in placenta-derived markers and later autistic traits in children
title_full_unstemmed Sex differences in placenta-derived markers and later autistic traits in children
title_short Sex differences in placenta-derived markers and later autistic traits in children
title_sort sex differences in placenta-derived markers and later autistic traits in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344956/
https://www.ncbi.nlm.nih.gov/pubmed/37443170
http://dx.doi.org/10.1038/s41398-023-02552-w
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