Mild internet use is associated with epigenetic alterations of key neurotransmission genes in salivary DNA of young university students
The potentially problematic use of the Internet is a growing concern worldwide, which causes and consequences are not completely understood yet. The neurobiology of Internet addiction (IA) has attracted much attention in scientific research, which is now focusing on identifying measurable biological...
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Published in | Scientific reports Vol. 13; no. 1; pp. 22192 - 14 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
14.12.2023
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | The potentially problematic use of the Internet is a growing concern worldwide, which causes and consequences are not completely understood yet. The neurobiology of Internet addiction (IA) has attracted much attention in scientific research, which is now focusing on identifying measurable biological markers. Aim of this study was to investigate epigenetic and genetic regulation of oxytocin receptor (
OXTR
), dopamine transporter (
DAT1
) and serotonin transporter (
SERT
) genes using DNA obtained from saliva samples of young university students: the Internet Addiction Test (IAT) was administered to evaluate the potential existence and intensity of IA. Significant changes in DNA methylation levels at
OXTR
,
DAT1
and
SERT
genes were observed in the 30 < IAT < 49 group (mild-risk internet users) compared to the IAT < 29 subjects (complete control of internet use) and IAT > 50 subjects (considered as moderately addicted). Moreover, epigenetic markers were significantly correlated, either directly (for
OXTR
and
DAT1
) or inversely (
OXTR
and
DAT1
versus
SERT
), to the psychometric properties. Our data confirmed the association of
OXTR
,
DAT1
and
SERT
genes in processes related to behavioural addictions and might be of relevance to suggest possible biological predictors of altered behaviours and the eventual vulnerability to develop an IA. Different other genetic pathways have been suggested to play a role in IA and research is ongoing to better define them, in order to help in the early diagnosis as well as in the development of new potential treatments. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-023-49492-5 |