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Shorter telomere length and suicidal ideation in familial bipolar disorder

Bipolar Disorder (BD) has recently been related to a process of accelerated aging, with shortened leukocyte telomere length (LTL) in this population. It has also been observed that the suicide rate in BD patients is higher than in the general population, and more recently the telomere length variati...

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Autores principales: Martinez, Daniela, Lavebratt, Catharina, Millischer, Vincent, de Jesus R. de Paula, Vanessa, Pires, Thiago, Michelon, Leandro, Camilo, Caroline, Esteban, Nubia, Pereira, Alexandre, Schalling, Martin, Vallada, Homero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721487/
https://www.ncbi.nlm.nih.gov/pubmed/36469522
http://dx.doi.org/10.1371/journal.pone.0275999
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author Martinez, Daniela
Lavebratt, Catharina
Millischer, Vincent
de Jesus R. de Paula, Vanessa
Pires, Thiago
Michelon, Leandro
Camilo, Caroline
Esteban, Nubia
Pereira, Alexandre
Schalling, Martin
Vallada, Homero
author_facet Martinez, Daniela
Lavebratt, Catharina
Millischer, Vincent
de Jesus R. de Paula, Vanessa
Pires, Thiago
Michelon, Leandro
Camilo, Caroline
Esteban, Nubia
Pereira, Alexandre
Schalling, Martin
Vallada, Homero
author_sort Martinez, Daniela
collection PubMed
description Bipolar Disorder (BD) has recently been related to a process of accelerated aging, with shortened leukocyte telomere length (LTL) in this population. It has also been observed that the suicide rate in BD patients is higher than in the general population, and more recently the telomere length variation has been described as shorter in suicide completers compared with control subjects. Objectives The aim of the present study was to investigate if there is an association between LTL and BD in families where two or more members have BD including clinical symptomatology variables, along with suicide behavior. Methods Telomere length and single copy gene ratio (T/S ratio) was measured using quantitative polymerase chain reaction in a sample of 143 relatives from 22 families, of which 60 had BD. The statistical analysis was performed with a polygenic mixed model. Results LTL was associated with suicidal ideation (p = 0.02) as that there is an interaction between suicidal ideation and course of the disorder (p = 0.02). The estimated heritability for LTL in these families was 0.68. In addition, covariates that relate to severity of disease, i.e. suicidal ideation and course of the disorder, showed an association with shorter LTL in BD patients. No difference in LTL between BD patients and healthy relatives was observed. Conclusion LTL are shorter in subjects with familial BD suggesting that stress related sub-phenotypes possibly accelerate the process of cellular aging and correlate with disease severity and suicidal ideation.
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spelling pubmed-97214872022-12-06 Shorter telomere length and suicidal ideation in familial bipolar disorder Martinez, Daniela Lavebratt, Catharina Millischer, Vincent de Jesus R. de Paula, Vanessa Pires, Thiago Michelon, Leandro Camilo, Caroline Esteban, Nubia Pereira, Alexandre Schalling, Martin Vallada, Homero PLoS One Research Article Bipolar Disorder (BD) has recently been related to a process of accelerated aging, with shortened leukocyte telomere length (LTL) in this population. It has also been observed that the suicide rate in BD patients is higher than in the general population, and more recently the telomere length variation has been described as shorter in suicide completers compared with control subjects. Objectives The aim of the present study was to investigate if there is an association between LTL and BD in families where two or more members have BD including clinical symptomatology variables, along with suicide behavior. Methods Telomere length and single copy gene ratio (T/S ratio) was measured using quantitative polymerase chain reaction in a sample of 143 relatives from 22 families, of which 60 had BD. The statistical analysis was performed with a polygenic mixed model. Results LTL was associated with suicidal ideation (p = 0.02) as that there is an interaction between suicidal ideation and course of the disorder (p = 0.02). The estimated heritability for LTL in these families was 0.68. In addition, covariates that relate to severity of disease, i.e. suicidal ideation and course of the disorder, showed an association with shorter LTL in BD patients. No difference in LTL between BD patients and healthy relatives was observed. Conclusion LTL are shorter in subjects with familial BD suggesting that stress related sub-phenotypes possibly accelerate the process of cellular aging and correlate with disease severity and suicidal ideation. Public Library of Science 2022-12-05 /pmc/articles/PMC9721487/ /pubmed/36469522 http://dx.doi.org/10.1371/journal.pone.0275999 Text en © 2022 Martinez et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Martinez, Daniela
Lavebratt, Catharina
Millischer, Vincent
de Jesus R. de Paula, Vanessa
Pires, Thiago
Michelon, Leandro
Camilo, Caroline
Esteban, Nubia
Pereira, Alexandre
Schalling, Martin
Vallada, Homero
Shorter telomere length and suicidal ideation in familial bipolar disorder
title Shorter telomere length and suicidal ideation in familial bipolar disorder
title_full Shorter telomere length and suicidal ideation in familial bipolar disorder
title_fullStr Shorter telomere length and suicidal ideation in familial bipolar disorder
title_full_unstemmed Shorter telomere length and suicidal ideation in familial bipolar disorder
title_short Shorter telomere length and suicidal ideation in familial bipolar disorder
title_sort shorter telomere length and suicidal ideation in familial bipolar disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721487/
https://www.ncbi.nlm.nih.gov/pubmed/36469522
http://dx.doi.org/10.1371/journal.pone.0275999
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