ABCB1 genotyping in the treatment of depression

被引:40
作者
Brueckl, Tanja Maria [1 ]
Uhr, Manfred [2 ]
机构
[1] Max Planck Inst Psychiat, Dept Translat Res Psychiat, Kraepelinstr 2-10, D-80804 Munich, Germany
[2] Max Planck Inst Psychiat, Clin Lab, Kraepelinstr 2-10, D-80804 Munich, Germany
关键词
ABCB1; genotyping; antidepressant response; antidepressant side effects; antidepressants; blood-brain barrier; gene; major depression; multidrug resistance; P-gp; pharmacogenetic test; pharmacokinetic gene; BLOOD-BRAIN-BARRIER; TREATMENT-RESISTANT DEPRESSION; GLYCOPROTEIN GENE DISRUPTION; ANTIDEPRESSANT-INDUCED MANIA; EFFLUX PROTEIN EXPRESSION; STAR-ASTERISK-D; P-GLYCOPROTEIN; MAJOR DEPRESSION; CLINICAL-RESPONSE; IN-VIVO;
D O I
10.2217/pgs.16.18
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
P-glycoprotein (P-gp), the gene product of ABCB1, is a drug transporter at the blood-brain barrier and could be a limiting factor for entrance of antidepressants into the brain, the target site of antidepressant action. Animal studies showed that brain concentrations of many antidepressants depend on P-gp. In humans, ABCB1 genotyping in the treatment of depression rests on the assumption that genetic variations in ABCB1 explain individual differences in antidepressant response via their effects on P-gp expression at the blood-brain barrier. High P-gp expression is hypothesized to lead to lower and often insufficient brain concentrations of P-gp substrate antidepressants. In this review, we summarize 32 studies investigating the question of whether ABCB1 polymorphisms predict clinical efficacy and/or tolerability of antidepressants in humans and evaluate the clinical application status of ABCB1 genotyping in depression treatment.
引用
收藏
页码:2039 / 2069
页数:31
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