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Ketone body 3-hydroxybutyrate as a biomarker of aggression

Human aggression is a complex behaviour, the biological underpinnings of which remain poorly known. To gain insights into aggression biology, we studied relationships with aggression of 11 low-molecular-weight metabolites (amino acids, ketone bodies), processed using (1)H nuclear magnetic resonance...

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Autores principales: Whipp, A. M., Vuoksimaa, E., Korhonen, T., Pool, R., But, A., Ligthart, L., Hagenbeek, F. A., Bartels, M., Bogl, L. H., Pulkkinen, L., Rose, R. J., Boomsma, D. I., Kaprio, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955062/
https://www.ncbi.nlm.nih.gov/pubmed/33712630
http://dx.doi.org/10.1038/s41598-021-84635-6
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author Whipp, A. M.
Vuoksimaa, E.
Korhonen, T.
Pool, R.
But, A.
Ligthart, L.
Hagenbeek, F. A.
Bartels, M.
Bogl, L. H.
Pulkkinen, L.
Rose, R. J.
Boomsma, D. I.
Kaprio, J.
author_facet Whipp, A. M.
Vuoksimaa, E.
Korhonen, T.
Pool, R.
But, A.
Ligthart, L.
Hagenbeek, F. A.
Bartels, M.
Bogl, L. H.
Pulkkinen, L.
Rose, R. J.
Boomsma, D. I.
Kaprio, J.
author_sort Whipp, A. M.
collection PubMed
description Human aggression is a complex behaviour, the biological underpinnings of which remain poorly known. To gain insights into aggression biology, we studied relationships with aggression of 11 low-molecular-weight metabolites (amino acids, ketone bodies), processed using (1)H nuclear magnetic resonance spectroscopy. We used a discovery sample of young adults and an independent adult replication sample. We studied 725 young adults from a population-based Finnish twin cohort born 1983–1987, with aggression levels rated in adolescence (ages 12, 14, 17) by multiple raters and blood plasma samples at age 22. Linear regression models specified metabolites as the response variable and aggression ratings as predictor variables, and included several potential confounders. All metabolites showed low correlations with aggression, with only one—3-hydroxybutyrate, a ketone body produced during fasting—showing significant (negative) associations with aggression. Effect sizes for different raters were generally similar in magnitude, while teacher-rated (age 12) and self-rated (age 14) aggression were both significant predictors of 3-hydroxybutyrate in multi-rater models. In an independent replication sample of 960 adults from the Netherlands Twin Register, higher aggression (self-rated) was also related to lower levels of 3-hydroxybutyrate. These exploratory epidemiologic results warrant further studies on the role of ketone metabolism in aggression.
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spelling pubmed-79550622021-03-15 Ketone body 3-hydroxybutyrate as a biomarker of aggression Whipp, A. M. Vuoksimaa, E. Korhonen, T. Pool, R. But, A. Ligthart, L. Hagenbeek, F. A. Bartels, M. Bogl, L. H. Pulkkinen, L. Rose, R. J. Boomsma, D. I. Kaprio, J. Sci Rep Article Human aggression is a complex behaviour, the biological underpinnings of which remain poorly known. To gain insights into aggression biology, we studied relationships with aggression of 11 low-molecular-weight metabolites (amino acids, ketone bodies), processed using (1)H nuclear magnetic resonance spectroscopy. We used a discovery sample of young adults and an independent adult replication sample. We studied 725 young adults from a population-based Finnish twin cohort born 1983–1987, with aggression levels rated in adolescence (ages 12, 14, 17) by multiple raters and blood plasma samples at age 22. Linear regression models specified metabolites as the response variable and aggression ratings as predictor variables, and included several potential confounders. All metabolites showed low correlations with aggression, with only one—3-hydroxybutyrate, a ketone body produced during fasting—showing significant (negative) associations with aggression. Effect sizes for different raters were generally similar in magnitude, while teacher-rated (age 12) and self-rated (age 14) aggression were both significant predictors of 3-hydroxybutyrate in multi-rater models. In an independent replication sample of 960 adults from the Netherlands Twin Register, higher aggression (self-rated) was also related to lower levels of 3-hydroxybutyrate. These exploratory epidemiologic results warrant further studies on the role of ketone metabolism in aggression. Nature Publishing Group UK 2021-03-12 /pmc/articles/PMC7955062/ /pubmed/33712630 http://dx.doi.org/10.1038/s41598-021-84635-6 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Whipp, A. M.
Vuoksimaa, E.
Korhonen, T.
Pool, R.
But, A.
Ligthart, L.
Hagenbeek, F. A.
Bartels, M.
Bogl, L. H.
Pulkkinen, L.
Rose, R. J.
Boomsma, D. I.
Kaprio, J.
Ketone body 3-hydroxybutyrate as a biomarker of aggression
title Ketone body 3-hydroxybutyrate as a biomarker of aggression
title_full Ketone body 3-hydroxybutyrate as a biomarker of aggression
title_fullStr Ketone body 3-hydroxybutyrate as a biomarker of aggression
title_full_unstemmed Ketone body 3-hydroxybutyrate as a biomarker of aggression
title_short Ketone body 3-hydroxybutyrate as a biomarker of aggression
title_sort ketone body 3-hydroxybutyrate as a biomarker of aggression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955062/
https://www.ncbi.nlm.nih.gov/pubmed/33712630
http://dx.doi.org/10.1038/s41598-021-84635-6
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