Dopamine D3 receptor Ser9Gly variant is associated with impulse control disorders in Parkinson's disease patients
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Date
2016-12
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Parkinsonism Relat Disord.
Abstract
Introduction: Impulse control disorders (ICD) are reported to occur at variable frequencies in different
ethnic groups. Genetic vulnerability is suspected to underlie the individual risk for ICD. We investigated
whether the allelic variants of dopamine (DRD3), glutamate (GRIN2B) and serotonin (HTR2A) receptors
are linked to ICD in Indian Parkinson’s disease (PD) patients.
Methods: We conducted a prospective, case-control study which included PD patients (70 with ICD, 100
without ICD categorized after direct psychiatric interview of patient and caregiver) and 285 healthy
controls. Single nucleotide polymorphism (SNP) variants of DRD3 p.S9G (rs6280), GRIN2B c.2664C>T
(rs1806201) and HTR2A c.102T>C (rs6313) were genotyped.
Results: Multivariate regression analysis revealed that DRD3 p.Ser9Gly (rs6280) heterozygous variant CT
(OR ¼ 2.22, 95% CI: 1.03e4.86, p ¼ 0.041), higher daily Levodopa equivalent doses (LED) of drugs (for
100 mg LED, OR ¼ 1.14, 95% CI: 1.01e1.29, p ¼ 0.041), current dopamine agonist but not Levodopa use
(OR ¼ 2.16, 95% CI: 1.03e4.55, p ¼ 0.042) and age of onset of motor symptoms under 50 years (OR 2.09,
95% CI: 1.05e4.18, p ¼ 0.035) were independently associated with ICD.
Conclusion: DRD3 p.Ser9Gly (rs6280) CT genotype is associated with ICD in Indian PD patients and this
association is novel. Enhanced D3 receptor affinity due to gain-of-function conferred by the glycine
residues could impair reward-risk assessment in the mesolimbic system and contribute to development
of impulsive behaviour, in carriers of this genotype.
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Citation
Krishnamoorthy S, Rajan R, Banerjee M, Kumar H, Sarma G, Krishnan S, Sarma S, Kishore A. Dopamine D3 receptor Ser9Gly variant is associated with impulse control disorders in Parkinson's disease patients. Parkinsonism Relat Disord. 2016 Sep;30:13-7.