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Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients
INTRODUCTION: Alcohol dependence and depression are often combined, patients with comorbid pathology have a more severe course of the disease, a high risk of suicide and therapeutic resistance. Enzyme dopamine-beta-hydroxylase (DBH) is a key player in a link between dopamine and norepinephrine neuro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9566373/ http://dx.doi.org/10.1192/j.eurpsy.2022.735 |
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author | Nikolishin, A. Chuprova, N. Kibitov, A. |
author_facet | Nikolishin, A. Chuprova, N. Kibitov, A. |
author_sort | Nikolishin, A. |
collection | PubMed |
description | INTRODUCTION: Alcohol dependence and depression are often combined, patients with comorbid pathology have a more severe course of the disease, a high risk of suicide and therapeutic resistance. Enzyme dopamine-beta-hydroxylase (DBH) is a key player in a link between dopamine and norepinephrine neuromediations and may be involved in alcohol dependence and depression comorbidity and genetic markers in DBH gene may be associated with the risk of comorbid state. OBJECTIVES: To test an association of DBH gene polymorphisms rs161111580 and rs1108580 with depression risk in alcohol-dependent patients. METHODS: Our sample consisted of 104 inpatients diagnosed by ICD-10 criteria: 40 with alcohol dependence (AD group) (age 45.6 (SD 10.853), 5% females), 64 with depression and alcoholism comorbidity (AD+D group) (age 41.2 (SD 9.903), 22% females) and 112 healthy controls (age 35.5 (SD 8.286), 15% females). rs1108580 and rs1611115 were detected by RT-PCR. RESULTS: For rs161111580, frequencies of minor T allele (p=0.031) and ТТ genotype (p=0.017) was higher, СС genotype (p=0.042) was lower in AD group vs. controls. rs161111580 T allele and TT genotype increases the risk of AD (OR=3.715, 95%CI [1.728-7.986], P=0.001 and OR=4.009, 95%CI [1.502-10.699], P=0.006). For rs161111580, frequency of ТТ genotype (p=0.009) was higher in AD+D group vs. controls. For rs1108580, frequency of major А allele (p=0.059, trend) was higher in AD+D, then in AD group. Major А allele rs1108580 increases the risk of depression in alcohol-dependent patients (OR=2.74, 95%CI [1.283-5.855], P=0.001). CONCLUSIONS: It was shown that the DBH rs1108580 increases the risk of depression in patients with alcohol dependence. DISCLOSURE: No significant relationships. |
format | Online Article Text |
id | pubmed-9566373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95663732022-10-17 Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients Nikolishin, A. Chuprova, N. Kibitov, A. Eur Psychiatry Abstract INTRODUCTION: Alcohol dependence and depression are often combined, patients with comorbid pathology have a more severe course of the disease, a high risk of suicide and therapeutic resistance. Enzyme dopamine-beta-hydroxylase (DBH) is a key player in a link between dopamine and norepinephrine neuromediations and may be involved in alcohol dependence and depression comorbidity and genetic markers in DBH gene may be associated with the risk of comorbid state. OBJECTIVES: To test an association of DBH gene polymorphisms rs161111580 and rs1108580 with depression risk in alcohol-dependent patients. METHODS: Our sample consisted of 104 inpatients diagnosed by ICD-10 criteria: 40 with alcohol dependence (AD group) (age 45.6 (SD 10.853), 5% females), 64 with depression and alcoholism comorbidity (AD+D group) (age 41.2 (SD 9.903), 22% females) and 112 healthy controls (age 35.5 (SD 8.286), 15% females). rs1108580 and rs1611115 were detected by RT-PCR. RESULTS: For rs161111580, frequencies of minor T allele (p=0.031) and ТТ genotype (p=0.017) was higher, СС genotype (p=0.042) was lower in AD group vs. controls. rs161111580 T allele and TT genotype increases the risk of AD (OR=3.715, 95%CI [1.728-7.986], P=0.001 and OR=4.009, 95%CI [1.502-10.699], P=0.006). For rs161111580, frequency of ТТ genotype (p=0.009) was higher in AD+D group vs. controls. For rs1108580, frequency of major А allele (p=0.059, trend) was higher in AD+D, then in AD group. Major А allele rs1108580 increases the risk of depression in alcohol-dependent patients (OR=2.74, 95%CI [1.283-5.855], P=0.001). CONCLUSIONS: It was shown that the DBH rs1108580 increases the risk of depression in patients with alcohol dependence. DISCLOSURE: No significant relationships. Cambridge University Press 2022-09-01 /pmc/articles/PMC9566373/ http://dx.doi.org/10.1192/j.eurpsy.2022.735 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Nikolishin, A. Chuprova, N. Kibitov, A. Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title | Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title_full | Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title_fullStr | Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title_full_unstemmed | Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title_short | Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients |
title_sort | polymorphism rs1108580 in dbh gene is associated with the risk of depression in alcohol-dependent patients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9566373/ http://dx.doi.org/10.1192/j.eurpsy.2022.735 |
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