Stuttering Research - Gene
Research
December 2008
Single nucleotide
polymorphisms of DAT and DRD2 genes in Han Chinese population
and their association with stuttering.
[Article in Chinese]
Pan CH, Song LP, DU J, Lan
J, Wu CM, Wu LJ, Lin L, Wang
W.
Graduate School of Chinese Academy of
Sciences, Beijing 100049, China.E-mail:
panchr05@mails.gucas.ac.cn.
OBJECTIVE: To explore the correlations of
dopamine transporter gene (DAT) and dopamine D(2) receptor gene
(DRD2) to stuttering. METHODS: To examine the correlations of
the 5 single nucleotide polymorphisms (SNPs) in dopaminergic
gene (C252T, C1804T, and C1820T in DAT gene, and T1054C and
C1072T in DRD(2) gene) to stuttering in Han Chinese
individuals, a case-control study involving 112 patients with
stuttering and 112 gender-matched controls was carried out.
Genotyping was performed by a combined approach using
polymerase chain reaction (PCR) and pyrosequencing. RESULTS:
C1804T showed no polymorphism in either the patients or the
control subjects and was therefore excluded from the following
analysis. The C allele frequency at C1072T site was
significantly higher, but T allele frequency significantly
lower in the stuttering group than in the control group. The
patients had significantly higher CC and lower CT genotype
frequencies than the control group. There were no significant
differences in the allelic frequencies of C252T, C1820T and
T1054C between the patients and the controls, suggesting a
Hardy-Weinberg equilibrium at these 3 loci. CONCLUSION: The
presence of the C allele at C1072T in DRD(2) gene is associated
with increased susceptibility to stuttering in Han Chinese,
whereas the T allele provides protection against the onset of
stuttering.
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