The effect of CYP2D6 variation on antipsychotic-induced hyperprolactinaemia: a systematic review and meta-analysis

被引:13
作者
Calafato, Maria Stella [1 ]
Austin-Zimmerman, Isabelle [1 ]
Thygesen, Johan H. [1 ,2 ]
Sairam, Mani [3 ]
Metastasio, Antonio [1 ]
Marston, Louise [4 ]
Abad-Santos, Francisco [5 ]
Bhat, Anjali [1 ]
Harju-Seppanen, Jasmine [1 ]
Irizar, Haritz [1 ]
Zartaloudi, Eirini [1 ]
Bramon, Elvira [1 ,6 ,7 ,8 ]
机构
[1] UCL, Div Psychiat, Mental Hlth Neurosci Res Dept, London, England
[2] UCL, Inst Hlth Informat, London, England
[3] Southern Hlth NHS Fdn Trust, Romsey Community Mental Hlth Team, London, England
[4] UCL, Dept Primary Care & Populat Hlth, London, England
[5] Univ Autonoma Madrid, Inst Teofilo Hernando, Inst Invest Sanitaria Princesa IP, Clin Pharmacol Dept,Hosp Univ la Princesa, Madrid, Spain
[6] Kings Coll London, Inst Psychiat Psychol & Neurosci, London, England
[7] South London & Maudsley NHS Fdn Trust, London, England
[8] UCL, Inst Cognit Neurosci, London, England
基金
英国惠康基金; 英国医学研究理事会; 欧盟地平线“2020”;
关键词
CYTOCHROME-P450; 2D6; CYP2D6; SCHIZOPHRENIC-PATIENTS; PROLACTIN LEVELS; MOLECULAR-GENETICS; RISPERIDONE; PHARMACOGENETICS; POLYMORPHISMS; PHARMACOKINETICS; PHARMACODYNAMICS; GENOTYPE;
D O I
10.1038/s41397-019-0142-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hyperprolactinemia is a known adverse drug reaction to antipsychotic treatment. Antipsychotic blood levels are influenced by cytochrome P450 enzymes, primarily CYP2D6. Variation in CYP450 genes may affect the risk of antipsychotic-induced hyperprolactinemia. We undertook a systematic review and meta-analysis to assess whether CYP2D6 functional genetic variants are associated with antipsychotic-induced hyperprolactinemia. The systematic review identified 16 relevant papers, seven of which were suitable for the meta-analysis (n = 303 participants including 134 extreme metabolisers). Participants were classified into four phenotype groups as poor, intermediate, extensive, and ultra-rapid metabolisers. A random effects meta-analysis was used and Cohen's d calculated as the effect size for each primary study. We found no significant differences in prolactin levels between CYP2D6 metabolic groups. Current evidence does not support using CYP2D6 genotyping to reduce risk of antipsychotic-induced hyperprolactinemia. However, statistical power is limited. Future studies with larger samples and including a range of prolactin-elevating drugs are needed.
引用
收藏
页码:629 / 637
页数:9
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