Detailed Information on Publication Record
2015
A 40-bp VNTR polymorphism in the 3 '-untranslated region of DAT1/SLC6A3 is associated with ADHD but not with alcoholism
ŠERÝ, Omar, Ivo PACLT, Ivana DRTÍLKOVÁ, Pavel THEINER, Marta KOPECKOVA et. al.Basic information
Original name
A 40-bp VNTR polymorphism in the 3 '-untranslated region of DAT1/SLC6A3 is associated with ADHD but not with alcoholism
Name in Czech
40-bp VNTR polymorfismus ve 3 ' nepřekládané oblasti genu pro DAT1 / SLC6A3 je asociován s ADHD nikoliv s alkoholismem
Authors
ŠERÝ, Omar (203 Czech Republic, guarantor, belonging to the institution), Ivo PACLT (203 Czech Republic), Ivana DRTÍLKOVÁ (203 Czech Republic, belonging to the institution), Pavel THEINER (203 Czech Republic, belonging to the institution), Marta KOPECKOVA (203 Czech Republic), Petr ZVOLSKÝ (203 Czech Republic) and Vladimír BALCAR (36 Australia)
Edition
Behavioral and Brain Functions, London, BIOMED CENTRAL LTD, 2015, 1744-9081
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30000 3. Medical and Health Sciences
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 1.720
RIV identification code
RIV/00216224:14310/15:00087478
Organization unit
Faculty of Science
UT WoS
000356474900001
Keywords in English
Hyperkinetic disorder; Polymorphism; Alcoholism; Dopamine transporter; miRNA
Tags
International impact, Reviewed
Změněno: 24/3/2016 14:41, Ing. Andrea Mikešková
V originále
Background: ADHD and alcoholism are psychiatric diseases with pathophysiology related to dopamine system. DAT1 belongs to the SLC6 family of transporters and is involved in the regulation of extracellular dopamine levels. A 40 bp variable number tandem repeat (VNTR) polymorphism in the 3'-untranslated region of DAT1/SLC6A3 gene was previously reported to be associated with various phenotypes involving disturbed regulation of dopaminergic neurotransmission. Methods: A total of 1312 subjects were included and genotyped for 40 bp VNTR polymorphism of DAT1/SLC6A3 gene in this study (441 alcoholics, 400 non-alcoholic controls, 218 ADHD children and 253 non ADHD children). Using miRBase software, we have performed a computer analysis of VNTR part of DAT1 gene for presence of miRNA binding sites. Results: We have found significant relationships between ADHD and the 40 bp VNTR polymorphisms of DAT1/SLC6A3 gene (P < 0.01). The 9/9 genotype appeared to reduce the risk of ADHD about 0.4-fold (p < 0.04). We also noted an occurrence of rare genotypes in ADHD (frequency different from controls at p < 0.01). No association between alcoholism and genotype frequencies of 40 bp VNTR polymorphism of DAT1/SLC6A3 gene has been detected. Conclusions: We have found an association between 40 bp VNTR polymorphism of DAT1/SLC6A3 gene and ADHD in the Czech population; in a broad agreement with studies in other population samples. Furthermore, we detected rare genotypes 8/10, 7/10 and 10/11 present in ADHD boys only and identified miRNAs that should be looked at as potential novel targets in the research on ADHD.
In Czech
Zjistili jsme souvislost mezi 40 bp VNTR polymorfismem genu pro DAT1 / SLC6A3 a ADHD v české populaci.. Dále jsme zjistili vzácné genotypy 8/10, 7/10 a 10/11 pouze u chlapců s ADHD.
Links
NR8137, research and development project |
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NR9298, research and development project |
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