Pharmacogenetics and Schizophrenia

被引:21
作者
Foster, Adriana [1 ]
Miller, Del D. [2 ]
Buckley, Peter [1 ]
机构
[1] Med Coll Georgia, Dept Psychiat & Hlth Behav, Augusta, GA 30912 USA
[2] Univ Iowa Carver Coll Med, Dept Psychiat, Iowa City, IA 52242 USA
关键词
Pharmacogenetics; Schizophrenia; Antipsychotics; Personalized medicine; DOPAMINE D3 RECEPTOR; INDUCED WEIGHT-GAIN; 1A2; CYP1A2; GENE; TARDIVE-DYSKINESIA; P-GLYCOPROTEIN; PROMOTER REGION; FUNCTIONAL POLYMORPHISM; TREATMENT RESPONSE; 1ST-EPISODE SCHIZOPHRENIA; ANTIPSYCHOTIC RESPONSE;
D O I
10.1016/j.cll.2010.07.010
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The wide interindividual variability in clinical response and tolerability of antipsychotic medications has led investigators to postulate that these variabilities may be under genetic control. Although not always consistent, there are promising indications from emergent pharmacogenetic studies that efficacy of antipsychotic medications for the various symptom domains of psychopathology in schizophrenia may be genetically regulated. This is an encouraging approach. Moreover, there are also suggestive findings that the side-effect profiles of second-generation antipsychotic medications and their propensity to cause weight gain and glucose and lipid abnormalities as well as tardive dyskinesia may be related to pharmacogenetic factors in this patient population. Ultimately, such approaches could drive choices of antipsychotic medication based on the likelihood of clinical response and development of side effects in light of a particular patient's genetic profile. In the future, this targeted approach (personalized medicine) may become informative for clinicians choosing an antipsychotic medication for an individual patient with schizophrenia.
引用
收藏
页码:975 / +
页数:20
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