Evidence map›Paper›PMID 25983551›Full record

ArticleBiomarker insights2015

Polymorphism in variable number of tandem repeats of dopamine d4 gene is a genetic risk factor in attention deficit hyperactive egyptian children: pilot study.

Ola Shahin, Nagwa A Meguid, Omnia Raafat, Reham M Dawood, Malak Doss, Noha G Bader El Din, Mostafa K El Awady

Open access · goldAbstract read
In one paragraph

Article in Biomarker insights, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Attention-deficit/hyperactive disorder updates.Frontiers in molecular neuroscience · 2022
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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

7 authors at 3 institutions in 1 country.

Ola ShahinProfessor of Psychiatry, Faculty of Medicine, Cairo University, Egypt.
Nagwa A MeguidProfessor of Human Genetics, National Research Center, Giza, Egypt.
Omnia RaafatProfessor of Psychiatry, Faculty of Medicine, Cairo University, Egypt.
Reham M DawoodResearcher of Molecular Genetics, Department of Microbial Biotechnology, National Research Center, Giza, Egypt.
Malak DossAssistant Researcher of Psychiatry, National Research Center, Giza, Egypt.
Noha G Bader El DinAssistant Professor of Molecular Genetics, Department of Microbial Biotechnology, National Research Center, Giza, Egypt.
Mostafa K El AwadyProfessor of Molecular Genetics, Department of Microbial Biotechnology, National Research Center, Giza, Egypt.
National Research Centre · EGCairo University · EGNational Water Research Center · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe variable number of tandem repeats (VNTR) of the dopamine receptor D4 (DRD4) gene among humans may elucidate individual differences in susceptibility to neuropsychiatric diseases. Dopamine dysfunction may be involved with Attention Deficit Hyperactivity Disorder (ADHD) symptoms. In this study, we report the association between the phenotype of ADHD, a condition characterized by inattentiveness, hyperactivity, and impulsiveness, and a 48-base pair VNTR in exon 3 of the DRD4 polymorphism. SUBJECTS AND

methodsWe used a case control approach conducted on 29 ADHD and 31 ethnically matched control Egyptian children (ages 6-12 years). Cases were assessed by a psychiatric semi-structured interview and the Conners' Parent Rating Scale. VNTR polymorphisms of the DRD4 gene were done by touchdown PCR program using exon 3-specific primers followed by agarose gel electrophoresis.

resultsWe observed a significant association between the existence of D4.4 allele of DRD4 and ADHD (P, 0.002); 6.9% of cases showed a single D4.4 and 10.3% showed a double D4.4 as compared to controls in whom D4.4 has never been detected.

conclusionChildren with smaller number of repeat alleles (two to four repeats) of the DRD4 gene have higher possibility to develop ADHD in Egyptian children.

Indexed as

ADHDDRD4VNTR

Identifiers

PMID25983551
PMCPMC4426936
OpenAlexW1482696263

What OpenQuestion holds

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Registered trials

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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.