Literature DB >> 19590515

Association between dopaminergic genes (SLC6A3 and DRD2) and stuttering among Han Chinese.

Jie Lan1, Manshu Song, Chunhui Pan, Guoqing Zhuang, Youxin Wang, Wenzhan Ma, Qiaoyun Chu, Qingxuan Lai, Feng Xu, Yanli Li, Lixin Liu, Wei Wang.   

Abstract

Normal function of the dopaminergic system is necessary for speech fluency. There was evidence that the activities of dopamine transporter (DAT) and dopamine D2 receptor (DRD2) could be altered in people with speech disfluency. This study aims to ascertain the possible correlation between two dopaminergic genes (SLC6A3 and DRD2) and disorder of speech fluency, and to determine the allelic frequencies of the five single-nucleotide polymorphisms (SNPs) (rs2617604, rs28364997, rs28364998 in SLC6A3 and rs6275, rs6277 in DRD2) among Han Chinese patients with this disorder. A sample of 112 patients with speech disfluency and 112 gender-matched controls were included in this case-control study. The results show that the presence of C allele at rs6277 in DRD2 gene is associated with increased susceptibility to the disorder, whereas T allele is protective. Haplotype 939T/957T is also a protective factor.

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Year:  2009        PMID: 19590515     DOI: 10.1038/jhg.2009.60

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  22 in total

Review 1.  Genetic bases of stuttering: the state of the art, 2011.

Authors:  Shelly Jo Kraft; Ehud Yairi
Journal:  Folia Phoniatr Logop       Date:  2012       Impact factor: 0.849

2.  Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.

Authors:  Muhammad Hashim Raza; Sheikh Riazuddin; Dennis Drayna
Journal:  Hum Genet       Date:  2010-08-13       Impact factor: 4.132

3.  Speech-induced suppression of evoked auditory fields in children who stutter.

Authors:  Deryk S Beal; Maher A Quraan; Douglas O Cheyne; Margot J Taylor; Vincent L Gracco; Luc F De Nil
Journal:  Neuroimage       Date:  2010-11-21       Impact factor: 6.556

4.  Evaluation of the association between polymorphisms at the DRD2 locus and stuttering.

Authors:  Changsoo Kang; Bianca Santos Domingues; Eduardo Sainz; Carlos Eduardo Frigério Domingues; Dennis Drayna; Danilo Moretti-Ferreira
Journal:  J Hum Genet       Date:  2011-03-10       Impact factor: 3.172

5.  Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.

Authors:  Catherine M Stein; Barbara Truitt; Fenghua Deng; Allison Avrich Ciesla; Feiyou Qiu; Peronne Joseph; Rekha Raghavendra; Jeremy Fondran; Robert P Igo; Jessica Tag; Lisa Freebairn; H Gerry Taylor; Barbara A Lewis; Sudha K Iyengar
Journal:  Psychiatr Genet       Date:  2014-10       Impact factor: 2.458

6.  Behavioral effects arising from the neural substrates for atypical planning and execution of word production in stuttering.

Authors:  Peter Howell
Journal:  Exp Neurol       Date:  2010-06-23       Impact factor: 5.330

7.  Young children's family history of stuttering and their articulation, language and attentional abilities: An exploratory study.

Authors:  Dahye Choi; Edward G Conture; Victoria Tumanova; Chagit E Clark; Tedra A Walden; Robin M Jones
Journal:  J Commun Disord       Date:  2017-11-26       Impact factor: 2.288

8.  Human GNPTAB stuttering mutations engineered into mice cause vocalization deficits and astrocyte pathology in the corpus callosum.

Authors:  Tae-Un Han; Jessica Root; Laura D Reyes; Elizabeth B Huchinson; Johann du Hoffmann; Wang-Sik Lee; Terra D Barnes; Dennis Drayna
Journal:  Proc Natl Acad Sci U S A       Date:  2019-08-12       Impact factor: 11.205

Review 9.  Stuttering: Clinical and research update.

Authors:  Hector R Perez; James H Stoeckle
Journal:  Can Fam Physician       Date:  2016-06       Impact factor: 3.275

Review 10.  Epidemiology of stuttering: 21st century advances.

Authors:  Ehud Yairi; Nicoline Ambrose
Journal:  J Fluency Disord       Date:  2012-11-27       Impact factor: 2.538

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