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Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders

OBJECTIVE: The features of childhood attention deficit hyperactivity disorder (ADHD) are significantly associated with adult mood disorders. Some genetic factors may be common to both ADHD and mood disorders underlie the association between these two phenotypes. The present study aimed to determine...

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Autores principales: Eun, Tae Kyung, Jeong, Seong Hoon, Lee, Kyu Young, Kim, Se Hyun, Ahn, Yong Min, Bang, Yang Weon, Joo, Eun-Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730929/
https://www.ncbi.nlm.nih.gov/pubmed/26792045
http://dx.doi.org/10.9758/cpn.2016.14.1.88
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author Eun, Tae Kyung
Jeong, Seong Hoon
Lee, Kyu Young
Kim, Se Hyun
Ahn, Yong Min
Bang, Yang Weon
Joo, Eun-Jeong
author_facet Eun, Tae Kyung
Jeong, Seong Hoon
Lee, Kyu Young
Kim, Se Hyun
Ahn, Yong Min
Bang, Yang Weon
Joo, Eun-Jeong
author_sort Eun, Tae Kyung
collection PubMed
description OBJECTIVE: The features of childhood attention deficit hyperactivity disorder (ADHD) are significantly associated with adult mood disorders. Some genetic factors may be common to both ADHD and mood disorders underlie the association between these two phenotypes. The present study aimed to determine whether a genetic role may be played by the serotonin transporter-linked polymorphic region (5-HTTLPR) in the childhood ADHD features of adult patients with mood disorders. METHODS: The present study included 232 patients with major depressive disorder (MDD), 154 patients with bipolar disorder (BPD), and 1,288 normal controls. Childhood ADHD features were assessed with the Korean version of the Wender Utah Rating Scale (WURS-K). The total score and the scores of three factors (impulsivity, inattention, and mood instability) from the WURS-K were analyzed to determine whether they were associated with the 5-HTTLPR genotype. RESULTS: In the BPD type II group, the 5-HTTLPR genotype was significantly associated with the total score (p=0.029) and the impulsivity factor (p=0.004) on the WURS-K. However, the inattention and mood instability factors were not associated with the 5-HTTLPR genotype. BPD type I, MDD and normal control groups did not exhibit any significant associations between the WURS-K scores and the 5-HTTLPR genotype. CONCLUSION: The findings suggest that the 5-HTTLPR genotype may play a role in the impulsivity component of childhood ADHD in patients with BPD type II. Because of a small sample size and a single candidate gene, further studies investigating other candidate genes using a larger sample are warranted to determine any common genetic links.
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spelling pubmed-47309292016-02-08 Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders Eun, Tae Kyung Jeong, Seong Hoon Lee, Kyu Young Kim, Se Hyun Ahn, Yong Min Bang, Yang Weon Joo, Eun-Jeong Clin Psychopharmacol Neurosci Original Article OBJECTIVE: The features of childhood attention deficit hyperactivity disorder (ADHD) are significantly associated with adult mood disorders. Some genetic factors may be common to both ADHD and mood disorders underlie the association between these two phenotypes. The present study aimed to determine whether a genetic role may be played by the serotonin transporter-linked polymorphic region (5-HTTLPR) in the childhood ADHD features of adult patients with mood disorders. METHODS: The present study included 232 patients with major depressive disorder (MDD), 154 patients with bipolar disorder (BPD), and 1,288 normal controls. Childhood ADHD features were assessed with the Korean version of the Wender Utah Rating Scale (WURS-K). The total score and the scores of three factors (impulsivity, inattention, and mood instability) from the WURS-K were analyzed to determine whether they were associated with the 5-HTTLPR genotype. RESULTS: In the BPD type II group, the 5-HTTLPR genotype was significantly associated with the total score (p=0.029) and the impulsivity factor (p=0.004) on the WURS-K. However, the inattention and mood instability factors were not associated with the 5-HTTLPR genotype. BPD type I, MDD and normal control groups did not exhibit any significant associations between the WURS-K scores and the 5-HTTLPR genotype. CONCLUSION: The findings suggest that the 5-HTTLPR genotype may play a role in the impulsivity component of childhood ADHD in patients with BPD type II. Because of a small sample size and a single candidate gene, further studies investigating other candidate genes using a larger sample are warranted to determine any common genetic links. Korean College of Neuropsychopharmacology 2016-02 2016-02-29 /pmc/articles/PMC4730929/ /pubmed/26792045 http://dx.doi.org/10.9758/cpn.2016.14.1.88 Text en Copyright © 2016, Korean College of Neuropsychopharmacology This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Eun, Tae Kyung
Jeong, Seong Hoon
Lee, Kyu Young
Kim, Se Hyun
Ahn, Yong Min
Bang, Yang Weon
Joo, Eun-Jeong
Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title_full Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title_fullStr Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title_full_unstemmed Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title_short Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders
title_sort association between the 5-httlpr genotype and childhood characteristics in mood disorders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730929/
https://www.ncbi.nlm.nih.gov/pubmed/26792045
http://dx.doi.org/10.9758/cpn.2016.14.1.88
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