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Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System

Methcathinone (ephedrone) is relatively easily accessible for abuse. Its users develop an extrapyramidal syndrome and it is not known if this is caused by methcathinone itself, by side-ingredients (manganese), or both. In the present study we aimed to clarify molecular mechanisms underlying this con...

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Autores principales: Sikk, Katrin, Kõks, Sulev, Soomets, Ursel, Schalkwyk, Leonard C., Fernandes, Cathy, Haldre, Sulev, Aquilonius, Sten-Magnus, Taba, Pille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268596/
https://www.ncbi.nlm.nih.gov/pubmed/22303338
http://dx.doi.org/10.3389/fgene.2011.00042
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author Sikk, Katrin
Kõks, Sulev
Soomets, Ursel
Schalkwyk, Leonard C.
Fernandes, Cathy
Haldre, Sulev
Aquilonius, Sten-Magnus
Taba, Pille
author_facet Sikk, Katrin
Kõks, Sulev
Soomets, Ursel
Schalkwyk, Leonard C.
Fernandes, Cathy
Haldre, Sulev
Aquilonius, Sten-Magnus
Taba, Pille
author_sort Sikk, Katrin
collection PubMed
description Methcathinone (ephedrone) is relatively easily accessible for abuse. Its users develop an extrapyramidal syndrome and it is not known if this is caused by methcathinone itself, by side-ingredients (manganese), or both. In the present study we aimed to clarify molecular mechanisms underlying this condition. We used microarrays to analyze whole-genome gene expression patterns of peripheral blood from 20 methcathinone users and 20 matched controls. Gene expression profile data were analyzed by Bayesian modeling and functional annotation. Of 28,869 genes on the microarrays, 326 showed statistically significant differential expression with FDR adjusted p-values below 0.05. Quantitative real-time PCR confirmed differential expression for the most of the genes selected for validation. Functional annotation and network analysis indicated activation of a gene network that included immunological disease, cellular movement, and cardiovascular disease functions (enrichment score 42). As HIV and HCV infections were confounding factors, we performed additional stratification of subjects. A similar functional activation of the “immunological disease” category was evident when we compared subjects according to injection status (past versus current users, balanced for HIV and HCV infection). However, this difference was not large therefore the major effect was related to the HIV status of the subjects. Mn–methcathinone abusers have blood RNA expression patterns that mostly reflect their HIV and HCV infections.
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spelling pubmed-32685962012-02-02 Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System Sikk, Katrin Kõks, Sulev Soomets, Ursel Schalkwyk, Leonard C. Fernandes, Cathy Haldre, Sulev Aquilonius, Sten-Magnus Taba, Pille Front Genet Genetics Methcathinone (ephedrone) is relatively easily accessible for abuse. Its users develop an extrapyramidal syndrome and it is not known if this is caused by methcathinone itself, by side-ingredients (manganese), or both. In the present study we aimed to clarify molecular mechanisms underlying this condition. We used microarrays to analyze whole-genome gene expression patterns of peripheral blood from 20 methcathinone users and 20 matched controls. Gene expression profile data were analyzed by Bayesian modeling and functional annotation. Of 28,869 genes on the microarrays, 326 showed statistically significant differential expression with FDR adjusted p-values below 0.05. Quantitative real-time PCR confirmed differential expression for the most of the genes selected for validation. Functional annotation and network analysis indicated activation of a gene network that included immunological disease, cellular movement, and cardiovascular disease functions (enrichment score 42). As HIV and HCV infections were confounding factors, we performed additional stratification of subjects. A similar functional activation of the “immunological disease” category was evident when we compared subjects according to injection status (past versus current users, balanced for HIV and HCV infection). However, this difference was not large therefore the major effect was related to the HIV status of the subjects. Mn–methcathinone abusers have blood RNA expression patterns that mostly reflect their HIV and HCV infections. Frontiers Research Foundation 2011-08-19 /pmc/articles/PMC3268596/ /pubmed/22303338 http://dx.doi.org/10.3389/fgene.2011.00042 Text en Copyright © 2011 Sikk, Kõks, Soomets, Schalkwyk, Fernandes, Haldre, Aquilonius and Taba. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Genetics
Sikk, Katrin
Kõks, Sulev
Soomets, Ursel
Schalkwyk, Leonard C.
Fernandes, Cathy
Haldre, Sulev
Aquilonius, Sten-Magnus
Taba, Pille
Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title_full Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title_fullStr Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title_full_unstemmed Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title_short Peripheral Blood RNA Expression Profiling in Illicit Methcathinone Users Reveals Effect on Immune System
title_sort peripheral blood rna expression profiling in illicit methcathinone users reveals effect on immune system
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268596/
https://www.ncbi.nlm.nih.gov/pubmed/22303338
http://dx.doi.org/10.3389/fgene.2011.00042
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