Evidence map›Paper›PMID 25568476›Full record

ArticleIndian journal of psychiatry2014

T102C polymorphism of serotonin-2A receptor gene in Turkish schizophrenia patients: Association with cognitive impairment and soft neurological signs.

Adnan Özçetin, Burç Çağrı Poyraz, Cana Aksoy Poyraz, Erol Bozhüyük, Nurullah Bolat, İbrahim Balcioğlu, Anıl Çağla Özkiliç, Zehra Seda Genç, Müjgan Cengiz

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Article in Indian journal of psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Article
4 · The record

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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

9 authors at 3 institutions in 1 country.

Adnan ÖzçetinDepartment of Psychiatry, Bolu İzzet Baysal Medical School, Bolu, Turkey.
Burç Çağrı PoyrazDepartment of Psychiatry, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Cana Aksoy PoyrazDepartment of Psychiatry, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Erol BozhüyükDepartment of Psychiatry, Kahramanmaraş State Hospital, Kahramanmaraş, Turkey.
Nurullah BolatDepartment of Child and Adolescent Psychiatry, Diyarbakır Pediatric Hospital, Diyarbakır, Turkey.
İbrahim BalcioğluDepartment of Psychiatry, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Anıl Çağla ÖzkiliçDepartment of Medical Biology, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Zehra Seda GençDepartment of Medical Biology, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Müjgan CengizDepartment of Medical Biology, University of Istanbul, Cerrahpaşa Medical School, Istanbul, Turkey.
Bolu Abant İzzet Baysal University · TRDiyarbakır Askeri Hastanesi · TRKahramanmaraş Sütçü İmam University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimPrevious studies have shown an association between the T102C polymorphism of the serotonin-2A receptor gene and schizophrenia. In addition, an association of this polymorphism with clinical phenotypes in schizophrenia such as treatment response and cognitive impairment has been observed. MATERIALS AND

methodsIn this case-control study conducted in Turkish Caucasians, we compared T102C polymorphism genotype and allele frequencies in 76 schizophrenic patients and 165 healthy controls. We also investigated interaction of this polymorphism with clinical and cognitive variables in patients.

resultsNo significant difference was observed in the distribution of the three genotypes (T/T, T/C and C/C) and in the allele frequencies in controls and patients with schizophrenia. No evidence of association was detected at various clinical phenotypes including symptom severity, suicidality, treatment response, age of disease onset, number of hospitalizations and history of violence (in co-dominant, dominant, or recessive models). However, as compared to the C/C genotype, patients with 1 or 2 copies of the T allele were characterized by better stroop test performances and less "motor coordination" soft neurological signs.

conclusionFurther research is needed to elucidate the impact of T102C polymorphism on neurocognitive functions in both healthy and patient populations.

Indexed as

Cognitive impairmentgene polymorphismneurological soft signsschizophreniaserotonin-2A receptor gene

Identifiers

PMID25568476
PMCPMC4279293
OpenAlexW256176963

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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.