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老年患者中舍曲林对映体和代谢物的血浆水平。

Plasma levels of citalopram enantiomers and metabolites in elderly patients.

作者信息

Foglia J P, Pollock B G, Kirshner M A, Rosen J, Sweet R, Mulsant B

机构信息

Department of Psychiatry, University of Pittsburgh, School of Medicine, PA 15213, USA.

出版信息

Psychopharmacol Bull. 1997;33(1):109-12.

PMID:9133760
Abstract

Ten patients with dementia and significant behavioral disturbances (mean age of 77.2 +/- 8.2 years) received citalopram, 10 mg/day for 3 days, followed by 20 mg/day for 2 weeks. Six of the 10 patients completing 17 days of treatment had a clinically impressive response, as assessed by significant improvement in six target items on the Neurobehavioral Rating Scale. Eight patients were also analyzed by measuring the racemic and enantiomeric plasma levels of citalopram (CIT) and desmethylcitalopram (DCIT). A sensitive high-performance liquid chromatography (HPLC) assay for citalopram enantiomers and metabolites was developed using ultraviolet detection. The lower limit of detection was 10 ng/ml for each enantiomer. Steady-state plasma level ranges were 11.2 to 92.2 ng/ml for the biologically active S(+) citalopram and 12.8 to 95.7 ng/ml for the inactive R(-) enantiomer. For the S and R enantiomers of desmethylcitalopram, plasma levels ranged from 11.0 to 22.0 ng/ml and 9.2 to 22.0 ng/ml, respectively. The racemic citalopram plasma level to dose ratio of 3.50 was higher than the ratio (1.96) reported by Overo (1982) for 55 younger patients. The stereoselective metabolism of the enantiomers for citalopram and desmethylcitalopram (S(+) and R(-) enantiomers) in these older subjects differed from that reported in younger patients, suggesting possible age-associated changes in CYP2C19 activities. We hypothesize that quantification of S(+) citalopram will permit a more accurate examination of dose/response relationships. This measure seems to be especially important for older subjects, given the wide ranges and higher concentrations evident from our preliminary results.

摘要

10名患有痴呆症且伴有明显行为障碍的患者(平均年龄77.2±8.2岁)接受了西酞普兰治疗,初始剂量为10毫克/天,持续3天,随后为20毫克/天,持续2周。在完成17天治疗的10名患者中,有6名患者有明显的临床反应,这是通过神经行为评定量表上6个目标项目的显著改善来评估的。还对8名患者进行了分析,测量了西酞普兰(CIT)和去甲西酞普兰(DCIT)的外消旋体和对映体血浆水平。采用紫外检测法建立了一种灵敏的高效液相色谱(HPLC)法,用于测定西酞普兰对映体及其代谢产物。每种对映体的检测下限为10纳克/毫升。生物活性的S(+)西酞普兰的稳态血浆水平范围为11.2至92.2纳克/毫升,无活性的R(-)对映体为12.8至95.7纳克/毫升。去甲西酞普兰的S和R对映体的血浆水平分别为11.0至22.0纳克/毫升和9.2至22.0纳克/毫升。外消旋体西酞普兰的血浆水平与剂量比为3.50,高于Overo(1982年)报道的55名年轻患者的比值(1.96)。这些老年受试者中西酞普兰和去甲西酞普兰对映体(S(+)和R(-)对映体)的立体选择性代谢与年轻患者中报道的不同,提示CYP2C19活性可能存在与年龄相关的变化。我们假设,对S(+)西酞普兰进行定量将有助于更准确地研究剂量/反应关系。鉴于我们初步结果中明显的广泛范围和较高浓度,这一措施对老年受试者似乎尤为重要。

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