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Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder
BACKGROUND: In previous studies we found mild deficiencies of circulating T cells in patients with bipolar disorder (BD) and children at risk for BD, correlating to a higher inflammatory state. The genetic and environmental influences on these T cell deficiencies in association with BD development a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368934/ https://www.ncbi.nlm.nih.gov/pubmed/30739250 http://dx.doi.org/10.1186/s40345-018-0139-3 |
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author | Snijders, G. Brouwer, R. Kemner, S. Bootsman, F. Drexhage, H. A. Hillegers, M. H. J. |
author_facet | Snijders, G. Brouwer, R. Kemner, S. Bootsman, F. Drexhage, H. A. Hillegers, M. H. J. |
author_sort | Snijders, G. |
collection | PubMed |
description | BACKGROUND: In previous studies we found mild deficiencies of circulating T cells in patients with bipolar disorder (BD) and children at risk for BD, correlating to a higher inflammatory state. The genetic and environmental influences on these T cell deficiencies in association with BD development are unknown. OBJECTIVES: The aim is to quantify genetic and environmental factors that contribute to the association between the liability to develop BD and T cell deficiencies. METHODS: Participants of a Dutch bipolar twin study (11 monozygotic BD twin pairs, 15 dizygotic BD twin pairs, 15 monozygotic and 12 dizygotic healthy twin pairs) were included. A detailed FACS analysis of frozen stored leukocytes was carried out to determine the percentages of T cells and various other leukocyte and lymphocyte subsets. A bivariate liability threshold twin model was used to determine genetic and environmental (common and unique) influences on the correlation between BD and the various subsets. RESULTS: Lower percentages of T cells and higher percentages of NK cells were associated with the familial liability to develop BD. Neither genetic nor shared or unique environmental factors could explain the associations. Lithium usage explained part of the association for T cells, smoking in part that for NK cells. CONCLUSIONS: Our results confirm that BD is the result of a complex interaction between various genetic and environmental risk factors, in which T and NK cells act as important intermediate immune players. |
format | Online Article Text |
id | pubmed-6368934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-63689342019-02-28 Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder Snijders, G. Brouwer, R. Kemner, S. Bootsman, F. Drexhage, H. A. Hillegers, M. H. J. Int J Bipolar Disord Short Communication BACKGROUND: In previous studies we found mild deficiencies of circulating T cells in patients with bipolar disorder (BD) and children at risk for BD, correlating to a higher inflammatory state. The genetic and environmental influences on these T cell deficiencies in association with BD development are unknown. OBJECTIVES: The aim is to quantify genetic and environmental factors that contribute to the association between the liability to develop BD and T cell deficiencies. METHODS: Participants of a Dutch bipolar twin study (11 monozygotic BD twin pairs, 15 dizygotic BD twin pairs, 15 monozygotic and 12 dizygotic healthy twin pairs) were included. A detailed FACS analysis of frozen stored leukocytes was carried out to determine the percentages of T cells and various other leukocyte and lymphocyte subsets. A bivariate liability threshold twin model was used to determine genetic and environmental (common and unique) influences on the correlation between BD and the various subsets. RESULTS: Lower percentages of T cells and higher percentages of NK cells were associated with the familial liability to develop BD. Neither genetic nor shared or unique environmental factors could explain the associations. Lithium usage explained part of the association for T cells, smoking in part that for NK cells. CONCLUSIONS: Our results confirm that BD is the result of a complex interaction between various genetic and environmental risk factors, in which T and NK cells act as important intermediate immune players. Springer Berlin Heidelberg 2019-02-10 /pmc/articles/PMC6368934/ /pubmed/30739250 http://dx.doi.org/10.1186/s40345-018-0139-3 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Short Communication Snijders, G. Brouwer, R. Kemner, S. Bootsman, F. Drexhage, H. A. Hillegers, M. H. J. Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title | Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title_full | Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title_fullStr | Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title_full_unstemmed | Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title_short | Genetic and environmental influences on circulating NK and T cells and their relation to bipolar disorder |
title_sort | genetic and environmental influences on circulating nk and t cells and their relation to bipolar disorder |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368934/ https://www.ncbi.nlm.nih.gov/pubmed/30739250 http://dx.doi.org/10.1186/s40345-018-0139-3 |
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