Evidence map›Paper›PMID 31159911›Full record

ArticleCNS spectrums2020

Problematic internet use: an exploration of associations between cognition and COMT rs4818, rs4680 haplotypes.

Konstantinos Ioannidis, Sarah A Redden, Stephanie Valle, Samuel R Chamberlain, Jon E Grant

Open access · greenAbstract read
In one paragraph

Article in CNS spectrums, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Similarities and Differences in Genetics.Advances in experimental medicine and biology · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Konstantinos IoannidisDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-1537-5425
Sarah A ReddenDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois, USA.
Stephanie ValleDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois, USA.
Samuel R ChamberlainDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-7014-8121
Jon E GrantDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0001-7784-7021
University of Chicago · USUniversity of Cambridge · GB

Funding

Wellcome Trust 110049
6 · The paper itself

Abstract

objectiveProblematic internet users suffer from impairment in a variety of cognitive domains. Research suggests that COMT haplotypes exert differential effects on cognition. We sought to investigate differences in the genetic profiles of problematic internet users and whether those could shed light on potential cognitive differences.

methodsWe recruited 206 non-treatment seeking participants with heightened impulsive traits and obtained cross-sectional demographic, clinical, and cognitive data as well as the genetic haplotypes of COMT rs4680 and rs4818. We identified 24 participants who presented with problematic internet use (PIU) and compared PIU and non-PIU participants using one-way analysis of variance (ANOVA) and chi square as appropriate.

resultsPIU was associated with worse performance on decision making, rapid visual processing, and spatial working memory tasks. Genetic variants were associated with altered cognitive performance, but rates of PIU did not statistically differ for particular haplotypes of COMT.

conclusionThis study indicates that PIU is characterized by deficits in decision making and working memory domains; it also provides evidence for elevated impulsive responses and impaired target detection on a sustained attention task, which is a novel area worth exploring further in future work. The effects observed in the genetic influences on cognition of PIU subjects imply that the genetic heritable components of PIU may not lie within the genetic loci influencing COMT function and cognitive performance; or that the genetic component in PIU involves many genetic polymorphisms each conferring only a small effect.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultCatechol O-MethyltransferaseCognitionDecision MakingFemaleHaplotypesHumansInternet Addiction DisorderMaleCatechol O-MethyltransferaseCOMT protein, humancognitionCOMTgeneticsinternet addictionProblematic internet use

Identifiers

PMID31159911
PMCPMC7292732
OpenAlexW2948739412

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.