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Decreased FMR1 mRNA levels found in men with substance use disorders

FMR1 gene (fragile X mental retardation 1) represents a genetic and epigenetic factor in a number of human diseases. Though the role of FMR1 gene in substance use disorders (SUDs) is not well studied, a number of investigations indicate that SUDs and FMR1-accociated disorders may share common underl...

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Autores principales: Krasteva, Maria, Koycheva, Yana, Racheva, Rositsa, Taseva, Teodora, Raycheva, Tsveta, Simeonova, Stiliana, Andreev, Boryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575801/
https://www.ncbi.nlm.nih.gov/pubmed/33102869
http://dx.doi.org/10.1016/j.heliyon.2020.e05270
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author Krasteva, Maria
Koycheva, Yana
Racheva, Rositsa
Taseva, Teodora
Raycheva, Tsveta
Simeonova, Stiliana
Andreev, Boryan
author_facet Krasteva, Maria
Koycheva, Yana
Racheva, Rositsa
Taseva, Teodora
Raycheva, Tsveta
Simeonova, Stiliana
Andreev, Boryan
author_sort Krasteva, Maria
collection PubMed
description FMR1 gene (fragile X mental retardation 1) represents a genetic and epigenetic factor in a number of human diseases. Though the role of FMR1 gene in substance use disorders (SUDs) is not well studied, a number of investigations indicate that SUDs and FMR1-accociated disorders may share common underlying mechanisms. We examined the relative FMR1 mRNA levels and their sex-distribution in leukocytes from patients with alcohol and drug dependence compared to healthy controls. The study included 44 participants, 16 with alcohol dependence (mean age 43, 10 males and 6 females), 17 with drug dependence (mean age 41, 12 males and 5 females) and 11 healthy controls (mean age 47, 5 males and 6 females). Participants donated 5–6 ml of blood and completed a specialized questionnaire. Total RNA was isolated and cDNA was synthesized and used as a template for qRT-PCR analysis. The studied persons with alcohol and drug dependence share common socio-demographic and substance-use related characteristics. Significant FMR1 down-regulation was observed in the alcohol dependent group (25 % decrease; p = 0.005). Sex-associated analysis revealed that FMR1 down-regulation was primarily in alcohol-dependent men (40% decrease; p = 0.001) and did not reach significance in women. A similar sex-dependent pattern was observed among drug-dependent individuals. Drug-dependent men had significantly lower FMR1 mRNA levels (24% decrease; p = 0.015) compared with controls, while no significant difference was observed in drug-dependent females. These data indicate FMR1 mRNA down-regulation in persons with alcohol- and drug-dependence, relative to controls, is sex-dependent. This implies a role for FMR1 in substance use disorders. These findings require confirmation by including protein measures and the recruitment of larger cohorts.
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spelling pubmed-75758012020-10-23 Decreased FMR1 mRNA levels found in men with substance use disorders Krasteva, Maria Koycheva, Yana Racheva, Rositsa Taseva, Teodora Raycheva, Tsveta Simeonova, Stiliana Andreev, Boryan Heliyon Research Article FMR1 gene (fragile X mental retardation 1) represents a genetic and epigenetic factor in a number of human diseases. Though the role of FMR1 gene in substance use disorders (SUDs) is not well studied, a number of investigations indicate that SUDs and FMR1-accociated disorders may share common underlying mechanisms. We examined the relative FMR1 mRNA levels and their sex-distribution in leukocytes from patients with alcohol and drug dependence compared to healthy controls. The study included 44 participants, 16 with alcohol dependence (mean age 43, 10 males and 6 females), 17 with drug dependence (mean age 41, 12 males and 5 females) and 11 healthy controls (mean age 47, 5 males and 6 females). Participants donated 5–6 ml of blood and completed a specialized questionnaire. Total RNA was isolated and cDNA was synthesized and used as a template for qRT-PCR analysis. The studied persons with alcohol and drug dependence share common socio-demographic and substance-use related characteristics. Significant FMR1 down-regulation was observed in the alcohol dependent group (25 % decrease; p = 0.005). Sex-associated analysis revealed that FMR1 down-regulation was primarily in alcohol-dependent men (40% decrease; p = 0.001) and did not reach significance in women. A similar sex-dependent pattern was observed among drug-dependent individuals. Drug-dependent men had significantly lower FMR1 mRNA levels (24% decrease; p = 0.015) compared with controls, while no significant difference was observed in drug-dependent females. These data indicate FMR1 mRNA down-regulation in persons with alcohol- and drug-dependence, relative to controls, is sex-dependent. This implies a role for FMR1 in substance use disorders. These findings require confirmation by including protein measures and the recruitment of larger cohorts. Elsevier 2020-10-17 /pmc/articles/PMC7575801/ /pubmed/33102869 http://dx.doi.org/10.1016/j.heliyon.2020.e05270 Text en © 2020 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Krasteva, Maria
Koycheva, Yana
Racheva, Rositsa
Taseva, Teodora
Raycheva, Tsveta
Simeonova, Stiliana
Andreev, Boryan
Decreased FMR1 mRNA levels found in men with substance use disorders
title Decreased FMR1 mRNA levels found in men with substance use disorders
title_full Decreased FMR1 mRNA levels found in men with substance use disorders
title_fullStr Decreased FMR1 mRNA levels found in men with substance use disorders
title_full_unstemmed Decreased FMR1 mRNA levels found in men with substance use disorders
title_short Decreased FMR1 mRNA levels found in men with substance use disorders
title_sort decreased fmr1 mrna levels found in men with substance use disorders
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575801/
https://www.ncbi.nlm.nih.gov/pubmed/33102869
http://dx.doi.org/10.1016/j.heliyon.2020.e05270
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