Evidence map›Paper›PMID 32691279›Full record

ArticleJournal of molecular neuroscience : MN2021

CDH13 and LPHN3 Gene Polymorphisms in Attention-Deficit/Hyperactivity Disorder: Their Relation to Clinical Characteristics.

Ahmet Özaslan, Esra Güney, Mehmet Ali Ergün, İlyas Okur, Dilek Yapar

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Driver mutations in ADGRL3 are involved in the evolution of ependymoma.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  5. 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.

Ahmet ÖzaslanChild and Adolescent Psychiatry Department, Yıldırım Beyazıt Univesity Yenimahalle Training and Research Hospital, 2026. Street, Number: 4, Yenimahalle, Ankara, Turkey. drahmetozaslan@yahoo.com.ORCID https://orcid.org/0000-0001-7741-201X
Esra GüneyChild and Adolescent Psychiatry Department, Gazi University Medical Faculty, Ankara, Turkey.
Mehmet Ali ErgünMedical Genetics Department, Gazi University Medical Faculty, Ankara, Turkey.
İlyas OkurDepartment of Child Health and Diseases, Gazi University Medical Faculty, Ankara, Turkey.
Dilek YaparPublic Health Department, Gazi University Medical Faculty, Ankara, Turkey.
Gazi University · TRYahoo (Spain) · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic factors play a major role in the etiopathogenesis of attention-deficit/hyperactivity disorder (ADHD). In this study, we aimed to investigate the relationship between the CDH13 (rs6565113, rs11150556) and LPHN3 (rs6551665, rs6858066, rs1947274, rs2345039) gene polymorphisms and ADHD. We also sought to examine possible relationships between these polymorphisms and the clinical course and treatment response in ADHD. A total of 120 patients (79% boys), aged 6 to 18 years, newly diagnosed (medication-naïve) with ADHD according to the DSM-5 and a group of 126 controls (74% girls) were enrolled in the study. We examined the association between the aforementioned polymorphisms and ADHD. Univariate and multivariate logistic regression analysis were used to evaluate factors influencing the treatment response of ADHD. A significant difference was found between ADHD and control groups in terms of genotype distribution of the LPHN3 rs6551665 and rs1947274 polymorphisms. The results also showed that having the GG genotype of rs6551665 and CC genotype of rs1947274 of the LPHN3 gene was associated with risk for ADHD, and this relationship was more prominent in male participants. In the multivariate logistic regression model established with variables shown to have a significant relationship with treatment response, the presence of the GG genotype of the LPHN3 rs6551665 polymorphism and high severity of ADHD assessed by CGI-S were associated with poor response to treatment. This study is the first study to investigate the relationship between ADHD and these polymorphisms among Turkish adolescents. Our results imply that the LPHN3 rs6551665 and rs1947274 polymorphisms have a significant effect on ADHD in a Turkish population, and support previous observations that the presence of the GG genotype of the LPHN3 rs6551665 polymorphism may be associated with poor response to treatment in ADHD.

Indexed as

Polymorphism, Single NucleotideAdolescentAntigens, CDAtomoxetine HydrochlorideAttention Deficit Disorder with HyperactivityCadherinsChildDrug ResistanceFemaleGenotypeHumansLogistic ModelsMaleReceptors, G-Protein-CoupledReceptors, PeptideSocioeconomic FactorsADGRL3 protein, humanAntigens, CDAtomoxetine HydrochlorideCadherinsCDH1 protein, humanReceptors, G-Protein-CoupledReceptors, PeptideAttention-deficit/hyperactivity disorderCDH13LPHN3Response to treatment

Identifiers

PMID32691279
OpenAlexW3043825455

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.