Evidence map›Paper›PMID 22297068›Full record

ArticleJournal of psychiatry & neuroscience : JPN2012

Differential association between the norepinephrine transporter gene and ADHD: role of sex and subtype.

Sarojini M Sengupta, Natalie Grizenko, Geeta A Thakur, Johanne Bellingham, Rosherrie DeGuzman, Sandra Robinson, Marina TerStepanian, Anna Poloskia, S M Shaheen, Marie-Eve Fortier and 2 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Journal of psychiatry & neuroscience : JPN, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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  8. Facing the Methodological Challenge in Dissecting the Genetics of ADHD: A Case for Deep Phenotyping and Heterogeneity Reduction.Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent · 2020
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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

12 authors at 4 institutions in 2 countries.

Sarojini M SenguptaDouglas Hospital Research Centre, Verdun, Que.
Natalie Grizenko
Geeta A Thakur
Johanne Bellingham
Rosherrie DeGuzman
Sandra Robinson
Marina TerStepanian
Anna Poloskia
S M Shaheen
Marie-Eve Fortier
Zia Choudhry
Ridha Joober
Douglas College · CAMcGill University · CACentre For Human Genetics · INDouglas Mental Health University Institute · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundPharmacologic and animal studies have strongly implicated the norepinephrine transporter (NET) in the pathophysiology of attention-deficit/hyperactivity disorder (ADHD). We conducted a family-based study, with stratification based on sex and subtype, to test the association between 30 tag single-nucleotide polymorphisms (SNPs) within the gene encoding NET (SLC6A2) and ADHD.

methodsFamily-based association tests were conducted with the categorical diagnosis of ADHD, as well as quantitative phenotypes of clinical relevance (Conners Global Index for Teachers and Parents, and Child Behavior Checklist measures). Sliding window haplotype analysis was conducted with screening based on conditional power using PBAT.

resultsA previously reported association with rs3785143 was confirmed in this study. Further, extensive association was observed with haplotype blocks, with a differential pattern observed based on sex and subtype. The 5' region of the gene (encompassing haplotype block 1 and including a functional promoter SNP, rs28386840) showed an association with ADHD in girls (irrespective of subtype). A different region of the gene (distributed around haplo-type block 2) was associated with distinct behavioural phenotypes in boys. These findings are correlated with previously reported functional studies of gene variants in SLC6A2. LIMITATIONS: The most important limitation of the study is the small size of the groups resulting from the stratification based on sex followed by subtype.

conclusionThe results obtained in this family-based study suggest that haplotype blocks within different regions of SLC6A2 show differential association with the disorder based on sex and subtype. These associations may have been masked in previous studies when tests were conducted with pooled samples.

Indexed as

Attention Deficit Disorder with HyperactivityChildDiagnostic and Statistical Manual of Mental DisordersFamilyFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMaleNorepinephrine Plasma Membrane Transport ProteinsPolymorphism, Single NucleotideSex CharacteristicsNorepinephrine Plasma Membrane Transport ProteinsSLC6A2 protein, human

Identifiers

PMID22297068
PMCPMC3297073
OpenAlexW2003884136

What OpenQuestion holds

Textmetadata
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.