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CYP2D6*10等位基因对日本精神分裂症患者中氟哌啶醇及还原氟哌啶醇稳态血药浓度的影响。

Effects of the CYP2D6*10 allele on the steady-state plasma concentrations of haloperidol and reduced haloperidol in Japanese patients with schizophrenia.

作者信息

Mihara K, Suzuki A, Kondo T, Yasui N, Furukori H, Nagashima U, Otani K, Kaneko S, Inoue Y

机构信息

Department of Neuropsychiatry, Hirosaki University School of Medicine, Japan.

出版信息

Clin Pharmacol Ther. 1999 Mar;65(3):291-4. doi: 10.1016/S0009-9236(99)70108-6.

Abstract

BACKGROUND

The CYP2D6*10 (*10) allele that causes decreased CYP2D6 activity is present in Asians with a high frequency of about 50%. In this study we studied the effects of the *10 allele on the steady-state plasma concentrations (Css) of haloperidol and reduced haloperidol.

METHODS

The subjects were 67 Japanese inpatients with schizophrenia who had only the wild-type or *10 alleles. Thirty-four patients were homozygous for the wild-type allele, and 26 were heterozygous and 7 were homozygous for the *10 allele. All patients had been receiving 12 mg/day haloperidol for at least 2 weeks. Plasma concentrations of haloperidol and reduced haloperidol were measured by HPLC.

RESULTS

The mean +/- SD values of haloperidol Css in the patients with 0, 1, and 2 *10 alleles were 22.8+/-11.0, 30.1+/-10.6, and 31.2+/-21.2 nmol/L, respectively, and those values for reduced haloperidol were 6.1+/-2.9, 9.5+/-3.7, and 9.9+/-6.2 nmol/L, respectively. The mean haloperidol Css was significantly (P < .05) higher in the patients with 1 *10 allele than in those with no *10 alleles. The mean Css of reduced haloperidol was significantly (P < .05) higher in the patients with 1 and 2 *10 alleles than in those with no *10 alleles.

CONCLUSION

This study suggests that the *10 allele plays an important role in controlling the Css of both haloperidol and reduced haloperidol, especially in Asian subjects.

摘要

背景

导致细胞色素P450 2D6(CYP2D6)活性降低的CYP2D6*10(10)等位基因在亚洲人中的出现频率较高,约为50%。在本研究中,我们研究了10等位基因对氟哌啶醇及其还原代谢产物稳态血药浓度(Css)的影响。

方法

研究对象为67例仅携带野生型或10等位基因的日本精神分裂症住院患者。34例患者为野生型等位基因纯合子,26例为杂合子,7例为10等位基因纯合子。所有患者均接受12mg/天的氟哌啶醇治疗至少2周。采用高效液相色谱法测定氟哌啶醇及其还原代谢产物的血药浓度。

结果

携带0、1和2个10等位基因的患者,其氟哌啶醇Css的均值±标准差分别为22.8±11.小、30.1±10.6和31.2±21.2nmol/L,其还原代谢产物的相应值分别为6.1±2.9、9.5±3.7和9.9±6.2nmol/L。携带1个10等位基因的患者,其氟哌啶醇Css均值显著高于(P<0.05)无10等位基因的患者。携带1个和2个10等位基因的患者,其还原代谢产物的Css均值显著高于(P<0.05)无*10等位基因的患者。

结论

本研究提示,*10等位基因在控制氟哌啶醇及其还原代谢产物的Css方面起重要作用,尤其在亚洲人群中。

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