Evidence suggests that repeated or chronic ketamine use, as compared to acute ketamine users, posed a higher clinical risk of developing psychotic disorders, potentially related to the underlying chronic N-methyl-D-aspartate receptor (NMDAR) dysfunction, and a higher risk of suffering from schizophrenia particularly in those genetically susceptible, or genetically predisposed ketamine abusers. With ketamine infusion rises as a emerging hope as an acute treatment for depression and suicidality under the shadow of unknown longer term psychotomimetic effects peculiarly amongst repeated or chronic use, the current case-control study aims to investigate: a) if repeated or chronic ketamine use is associated with an increased risk of psychosis by comparing those ketamine abusers with and without psychosis, and to those non-ketamine-using drug abusers with psychosis; and b) if genetic predisposition from single nucleotide polymorphisms are associated with risk of psychosis in ketamine abusers.
Study Type
OBSERVATIONAL
Enrollment
162
blood sampling via venipuncture
Queen Mary Hospital
Hong Kong, Hong Kong
Western Psychiatric Centre
Hong Kong, Hong Kong
relative risk of ketamine users compared to non-ketamine using drug user to develop psychosis
relative risk of ketamine users compared to non-ketamine using drug user to develop psychosis
Time frame: During the 2 year study period
Gene association to development of psychcosis
The single nucleotide polymorphism of 4 genes associated with N-methyl-D-aspartate and dopamine receptors being associated with the development of psychosis in ketamine abuser
Time frame: During the 2 year study period
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