Effect of Valproate and Antidepressant Drugs on Clozapine Metabolism in Patients With Psychotic Mood Disorders

被引:9
作者
Marazziti, Donatella [1 ]
Palego, Lionella [1 ]
Betti, Laura [2 ]
Giannaccini, Gino [2 ]
Massimetti, Enrico [3 ]
Baroni, Stefano [1 ]
Ciapparelli, Antonio [1 ]
Lucacchini, Antonio [2 ]
Mucci, Federico [1 ]
Dell'Osso, Liliana [1 ]
机构
[1] Univ Pisa, Dept Expt & Clin Med, Psychiat Sect, Via Roma 67, I-56100 Pisa, Italy
[2] Univ Pisa, Dept Pharm, Pisa, Italy
[3] Osped Treviglio, ASST Bergamo Ovest SSD Serv Psichiat Diagnosi & C, Bergamo, Italy
关键词
clozapine; valproate; antidepressants; clozapine plasma parameters; NEUROLEPTIC-RESISTANT SCHIZOPHRENIA; LOW-DOSE CLOZAPINE; N-DESMETHYLCLOZAPINE; PLASMA-LEVELS; CLINICAL-RESPONSE; BIPOLAR DISORDER; LIQUID-CHROMATOGRAPHY; MAJOR METABOLITES; SCHIZOAFFECTIVE DISORDER; ATYPICAL ANTIPSYCHOTICS;
D O I
10.1097/FTD.0000000000000513
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
Background: The aim of the present study was to appraise retrospectively the influence of valproate (VPA) and antidepressants (ADs) on the steady-state plasma concentrations of clozapine (CLZ), the prototype of various second-generation antipsychotics, norclozapine (NCLZ, its main metabolite), and their ratio (NCLZ:CLZ). Methods: Sixty-seven psychotic patients with a prevalent diagnosis of bipolar disorder were studied. We then analyzed data altogether and subdivided them into 4 groups, according to pharmacological treatments: #1 CLZ (n = 21), #2 CLZ plus ADs (n = 13), #3 CLZ plus VPA (n = 16), and #4 CLZ plus ADs plus VPA (n = 17). Results: First, significant positive between CLZ and NCLZ plasma levels (in nanograms/milliliter) and the drug daily dosages (in milligrams/kilogram of body weight) (n = 67) were observed (Spear-man: rCLZ = 0.49; rNCLZ = 0.61; P < 0.001). We then normalized by given doses CLZ and NCLZ plasma levels, natural log transformed them, and performed analysis of variance factor analyses followed by pairwise comparisons, performed on the 4 groups and the 3 CLZ parameters. We identified significant drug effects on (1) CLZ plasma levels, significantly higher in group #2 versus group #1, and (2) NCLZ:CLZ ratio, lower in group #2 versus groups #1 and #3. Significant drug x gender interactions were observed in group #3, showing higher NCLZ levels and NCLZ:CLZ ratios in men compared with women. Conclusions: Despite its inherent limitations, this observational study confirms the significant increase in plasma CLZ concentrations and reduction in NCLZ:CLZ ratio when this drug was coadministered with ADs (group #2), an effect apparently counteracted by VPA (group #4). The drug x gender interactions in patients taking both CLZ and VPA (group #3) warrant further prospective study.
引用
收藏
页码:443 / 451
页数:9
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