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Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals

Polygenic risk for schizophrenia has been associated with lower cognitive ability and age-related cognitive change in healthy individuals. Despite well-established neuropsychological sex differences in schizophrenia patients, genetic studies on sex differences in schizophrenia in relation to cognit...

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Autores principales: Koch, Elise, Nyberg, Lars, Lundquist, Anders, Pudas, Sara, Adolfsson, Rolf, Kauppi, Karolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505489/
https://www.ncbi.nlm.nih.gov/pubmed/34635642
http://dx.doi.org/10.1038/s41398-021-01649-4
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author Koch, Elise
Nyberg, Lars
Lundquist, Anders
Pudas, Sara
Adolfsson, Rolf
Kauppi, Karolina
author_facet Koch, Elise
Nyberg, Lars
Lundquist, Anders
Pudas, Sara
Adolfsson, Rolf
Kauppi, Karolina
author_sort Koch, Elise
collection PubMed
description Polygenic risk for schizophrenia has been associated with lower cognitive ability and age-related cognitive change in healthy individuals. Despite well-established neuropsychological sex differences in schizophrenia patients, genetic studies on sex differences in schizophrenia in relation to cognitive phenotypes are scarce. Here, we investigated whether the effect of a polygenic risk score (PRS) for schizophrenia on childhood, midlife, and late-life cognitive function in healthy individuals is modified by sex, and if PRS is linked to accelerated cognitive decline. Using a longitudinal data set from healthy individuals aged 25–100 years (N = 1459) spanning a 25-year period, we found that PRS was associated with lower cognitive ability (episodic memory, semantic memory, visuospatial ability), but not with accelerated cognitive decline. A significant interaction effect between sex and PRS was seen on cognitive task performance, and sex-stratified analyses showed that the effect of PRS was male-specific. In a sub-sample, we observed a male-specific effect of the PRS on school performance at age 12 (N = 496). Our findings of sex-specific effects of schizophrenia genetics on cognitive functioning across the lifespan indicate that the effects of underlying disease genetics on cognitive functioning is dependent on biological processes that differ between the sexes.
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spelling pubmed-85054892021-10-27 Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals Koch, Elise Nyberg, Lars Lundquist, Anders Pudas, Sara Adolfsson, Rolf Kauppi, Karolina Transl Psychiatry Article Polygenic risk for schizophrenia has been associated with lower cognitive ability and age-related cognitive change in healthy individuals. Despite well-established neuropsychological sex differences in schizophrenia patients, genetic studies on sex differences in schizophrenia in relation to cognitive phenotypes are scarce. Here, we investigated whether the effect of a polygenic risk score (PRS) for schizophrenia on childhood, midlife, and late-life cognitive function in healthy individuals is modified by sex, and if PRS is linked to accelerated cognitive decline. Using a longitudinal data set from healthy individuals aged 25–100 years (N = 1459) spanning a 25-year period, we found that PRS was associated with lower cognitive ability (episodic memory, semantic memory, visuospatial ability), but not with accelerated cognitive decline. A significant interaction effect between sex and PRS was seen on cognitive task performance, and sex-stratified analyses showed that the effect of PRS was male-specific. In a sub-sample, we observed a male-specific effect of the PRS on school performance at age 12 (N = 496). Our findings of sex-specific effects of schizophrenia genetics on cognitive functioning across the lifespan indicate that the effects of underlying disease genetics on cognitive functioning is dependent on biological processes that differ between the sexes. Nature Publishing Group UK 2021-10-11 /pmc/articles/PMC8505489/ /pubmed/34635642 http://dx.doi.org/10.1038/s41398-021-01649-4 Text en © The Author(s) 2021 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
Koch, Elise
Nyberg, Lars
Lundquist, Anders
Pudas, Sara
Adolfsson, Rolf
Kauppi, Karolina
Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title_full Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title_fullStr Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title_full_unstemmed Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title_short Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
title_sort sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505489/
https://www.ncbi.nlm.nih.gov/pubmed/34635642
http://dx.doi.org/10.1038/s41398-021-01649-4
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