Association of the risk allele of dopamine transporter gene (DAT1*10) in Omani male children with attention-deficit hyperactivity disorder
Author: Simsek M, Al Sharbati M, Al Adawi S, Ganguly SS, Lawatia K.
Source:
Clinical biochemistry, 38(8), 739-742.
OBJECTIVES: To determine the frequency of the VNTR alleles in the human dopamine
transporter gene (DAT1) in the Omani population and to investigate association of
the VNTR alleles with attention-deficit hyperactivity disorder (ADHD). DESIGN AND
METHODS: 92 Omani children with ADHD and 110 healthy Omani subjects were
genotyped for the DAT1-VNTR polymorphism in a case-control study using two
independent PCR tests (one developed in our laboratory) followed by agarose gel
electrophoresis. RESULTS AND CONCLUSIONS: We determined the DAT1-VNTR alleles in
202 Omani subjects. There were two common alleles (DAT1*9 and *10) and five rare
ones. The DAT1*10 allele distribution was essentially the same both in the
control (60.9%) and the patient group (64.6%). There was, however, a relatively
higher occurrence of the DAT1*10 allele in ADHD males (69.4%) than females (55%),
but this gender difference was not present in the control group (males 60%,
females 62%).