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Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression

To elucidate a genetic predisposition to major depressive disorder, we investigated two polymorphisms (−31T/C and −511C/T) in the interleukin-1beta promoter region in patients who suffered from major recurrent depression. The aim of the current work was to compare alleles and genotype layout between...

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Autores principales: Borkowska, Paulina, Kucia, Krzysztof, Rzezniczek, Szymon, Paul-Samojedny, Monika, Kowalczyk, Malgorzata, Owczarek, Aleksander, Suchanek, Renata, Medrala, Tomasz, Kowalski, Jan
Formato: Texto
Lenguaje:English
Publicado: Humana Press Inc 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076565/
https://www.ncbi.nlm.nih.gov/pubmed/21465264
http://dx.doi.org/10.1007/s12031-011-9507-5
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author Borkowska, Paulina
Kucia, Krzysztof
Rzezniczek, Szymon
Paul-Samojedny, Monika
Kowalczyk, Malgorzata
Owczarek, Aleksander
Suchanek, Renata
Medrala, Tomasz
Kowalski, Jan
author_facet Borkowska, Paulina
Kucia, Krzysztof
Rzezniczek, Szymon
Paul-Samojedny, Monika
Kowalczyk, Malgorzata
Owczarek, Aleksander
Suchanek, Renata
Medrala, Tomasz
Kowalski, Jan
author_sort Borkowska, Paulina
collection PubMed
description To elucidate a genetic predisposition to major depressive disorder, we investigated two polymorphisms (−31T/C and −511C/T) in the interleukin-1beta promoter region in patients who suffered from major recurrent depression. The aim of the current work was to compare alleles and genotype layout between patients with major recurrent depression and healthy people. We would like to indicate such combination of genotypes which corresponds with major recurrent depression. Correlations between genotypes for analyzed polymorphisms and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset were investigated as well. The study group consisted of 94 patients diagnosed with major recurrent depression. The control group included 206 healthy individuals. Both groups involved representatives of Caucasian population. Genotyping of polymorphisms was performed by using PCR-RFLP technique. A specific haplotype, composed of the C allele at −31 and the T allele at −511, has a tendency to have a statistically significant difference (p = 0.064) between patients and control group. Correspondence analysis revealed that genotype T/T at −31 and genotype C/C at −511 are associated with major recurrent depression. No association was found between genotypes for studied polymorphic sites and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset.
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spelling pubmed-30765652011-05-23 Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression Borkowska, Paulina Kucia, Krzysztof Rzezniczek, Szymon Paul-Samojedny, Monika Kowalczyk, Malgorzata Owczarek, Aleksander Suchanek, Renata Medrala, Tomasz Kowalski, Jan J Mol Neurosci Article To elucidate a genetic predisposition to major depressive disorder, we investigated two polymorphisms (−31T/C and −511C/T) in the interleukin-1beta promoter region in patients who suffered from major recurrent depression. The aim of the current work was to compare alleles and genotype layout between patients with major recurrent depression and healthy people. We would like to indicate such combination of genotypes which corresponds with major recurrent depression. Correlations between genotypes for analyzed polymorphisms and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset were investigated as well. The study group consisted of 94 patients diagnosed with major recurrent depression. The control group included 206 healthy individuals. Both groups involved representatives of Caucasian population. Genotyping of polymorphisms was performed by using PCR-RFLP technique. A specific haplotype, composed of the C allele at −31 and the T allele at −511, has a tendency to have a statistically significant difference (p = 0.064) between patients and control group. Correspondence analysis revealed that genotype T/T at −31 and genotype C/C at −511 are associated with major recurrent depression. No association was found between genotypes for studied polymorphic sites and number of episodes, number of points in Hamilton Depression Rating Scale, and age of onset. Humana Press Inc 2011-04-05 2011 /pmc/articles/PMC3076565/ /pubmed/21465264 http://dx.doi.org/10.1007/s12031-011-9507-5 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Borkowska, Paulina
Kucia, Krzysztof
Rzezniczek, Szymon
Paul-Samojedny, Monika
Kowalczyk, Malgorzata
Owczarek, Aleksander
Suchanek, Renata
Medrala, Tomasz
Kowalski, Jan
Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title_full Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title_fullStr Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title_full_unstemmed Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title_short Interleukin-1beta Promoter (−31T/C and −511C/T) Polymorphisms in Major Recurrent Depression
title_sort interleukin-1beta promoter (−31t/c and −511c/t) polymorphisms in major recurrent depression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076565/
https://www.ncbi.nlm.nih.gov/pubmed/21465264
http://dx.doi.org/10.1007/s12031-011-9507-5
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