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Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome

The genetic predisposition toward suicidal ideation has been explored to identify subgroups at high risk and to prevent suicide. Acute coronary syndrome (ACS) is associated with an increased risk of suicide, but few studies have explored the genetic predisposition toward suicide in ACS populations....

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Autores principales: Kang, Hee-Ju, Bae, Kyung-Yeol, Kim, Sung-Wan, Shin, Il-Seon, Hong, Young Joon, Ahn, Youngkeun, Jeong, Myung Ho, Yoon, Jin-Sang, Kim, Jae-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706927/
https://www.ncbi.nlm.nih.gov/pubmed/29212281
http://dx.doi.org/10.18632/oncotarget.21661
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author Kang, Hee-Ju
Bae, Kyung-Yeol
Kim, Sung-Wan
Shin, Il-Seon
Hong, Young Joon
Ahn, Youngkeun
Jeong, Myung Ho
Yoon, Jin-Sang
Kim, Jae-Min
author_facet Kang, Hee-Ju
Bae, Kyung-Yeol
Kim, Sung-Wan
Shin, Il-Seon
Hong, Young Joon
Ahn, Youngkeun
Jeong, Myung Ho
Yoon, Jin-Sang
Kim, Jae-Min
author_sort Kang, Hee-Ju
collection PubMed
description The genetic predisposition toward suicidal ideation has been explored to identify subgroups at high risk and to prevent suicide. Acute coronary syndrome (ACS) is associated with an increased risk of suicide, but few studies have explored the genetic predisposition toward suicide in ACS populations. Therefore, this longitudinal study explored the genetic predisposition toward suicidal ideation in ACS patients. In total, of 969 patients within 2 weeks after ACS, 711 were followed at 1 year after ACS. Suicidal ideation was evaluated with the relevant items on the Montgomery–Åsberg Depression Rating Scale. Ten genetic polymorphisms associated with serotonergic systems, neurotrophic factors, carbon metabolism, and inflammatory cytokines were examined. Associations between genetic polymorphisms and suicidal ideation within 2 weeks and 1 year of ACS were investigated using logistic regression models. The 5-HTTLPR s allele was significantly associated with suicidal ideation within 2 weeks of ACS after adjusting for covariates and after the Bonferroni correction. TNF-α –308(G/A), IL-1β –511(C/T), and IL-1β + 3953C/T were significantly associated with suicidal ideation within 2 weeks after ACS, but these associations did not reach significance after the Bonferroni correction in unadjusted analyses and after adjusting for covariance. However, no significant association between genetic polymorphisms and suicidal ideation was found at 1 year. Genetic predisposition, 5-HTTLPR s allele in particular, may confer susceptibility to suicidal ideation in ACS patients during the acute phase of ACS.
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spelling pubmed-57069272017-12-05 Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome Kang, Hee-Ju Bae, Kyung-Yeol Kim, Sung-Wan Shin, Il-Seon Hong, Young Joon Ahn, Youngkeun Jeong, Myung Ho Yoon, Jin-Sang Kim, Jae-Min Oncotarget Clinical Research Paper The genetic predisposition toward suicidal ideation has been explored to identify subgroups at high risk and to prevent suicide. Acute coronary syndrome (ACS) is associated with an increased risk of suicide, but few studies have explored the genetic predisposition toward suicide in ACS populations. Therefore, this longitudinal study explored the genetic predisposition toward suicidal ideation in ACS patients. In total, of 969 patients within 2 weeks after ACS, 711 were followed at 1 year after ACS. Suicidal ideation was evaluated with the relevant items on the Montgomery–Åsberg Depression Rating Scale. Ten genetic polymorphisms associated with serotonergic systems, neurotrophic factors, carbon metabolism, and inflammatory cytokines were examined. Associations between genetic polymorphisms and suicidal ideation within 2 weeks and 1 year of ACS were investigated using logistic regression models. The 5-HTTLPR s allele was significantly associated with suicidal ideation within 2 weeks of ACS after adjusting for covariates and after the Bonferroni correction. TNF-α –308(G/A), IL-1β –511(C/T), and IL-1β + 3953C/T were significantly associated with suicidal ideation within 2 weeks after ACS, but these associations did not reach significance after the Bonferroni correction in unadjusted analyses and after adjusting for covariance. However, no significant association between genetic polymorphisms and suicidal ideation was found at 1 year. Genetic predisposition, 5-HTTLPR s allele in particular, may confer susceptibility to suicidal ideation in ACS patients during the acute phase of ACS. Impact Journals LLC 2017-10-07 /pmc/articles/PMC5706927/ /pubmed/29212281 http://dx.doi.org/10.18632/oncotarget.21661 Text en Copyright: © 2017 Kang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Kang, Hee-Ju
Bae, Kyung-Yeol
Kim, Sung-Wan
Shin, Il-Seon
Hong, Young Joon
Ahn, Youngkeun
Jeong, Myung Ho
Yoon, Jin-Sang
Kim, Jae-Min
Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title_full Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title_fullStr Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title_full_unstemmed Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title_short Genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
title_sort genetic predisposition toward suicidal ideation in patients with acute coronary syndrome
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706927/
https://www.ncbi.nlm.nih.gov/pubmed/29212281
http://dx.doi.org/10.18632/oncotarget.21661
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