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精神分裂症缺损型和非缺损型患者血浆3-甲氧基-4-羟基苯乙二醇和高香草酸的测定

Plasma 3-methoxy-4-hydroxyphenylglycol and homovanillic acid measurements in deficit and nondeficit forms of schizophrenia.

作者信息

Thibaut F, Ribeyre J M, Dourmap N, Ménard J F, Dollfus S, Petit M

机构信息

Groupe de Recherche Psychopathologie et Schizophrénies, Universités de Médecine de Rouen et Caen, Centre Hospitalier du Rouvray, France.

出版信息

Biol Psychiatry. 1998 Jan 1;43(1):24-30. doi: 10.1016/s0006-3223(97)00023-1.

Abstract

BACKGROUND

Discrepancies in the biochemical research on negative symptoms in schizophrenia may be ascribed to the lack of differentiation into primary and secondary negative symptoms. We have used Carpenter's criteria to define the deficit syndrome of schizophrenia as the presence of enduring and primary negative symptoms and measured catecholaminergic parameters in deficit as compared with nondeficit schizophrenics.

METHODS

We have investigated plasma homovanillic acid (pHVA) and 3-methoxy-4-hydroxyphenylglycol (pMHPG) concentrations in 34 DSM-III-R neuroleptic-treated schizophrenic patients who were classified into deficit (n = 14) and nondeficit (n = 20) forms of schizophrenia. All these patients were in a stable clinical and therapeutic status for the preceding 12 months.

RESULTS

The 14 deficit schizophrenic patients had lower plasma levels of pHVA and higher plasma concentrations of pMHPG from 9 AM to 12 AM as compared with the 20 nondeficit schizophrenic patients. The two groups did not differ on any demographic, therapeutic, or clinical variable considered.

CONCLUSIONS

Our data are consistent with the postulated distinct pathophysiological basis for the deficit syndrome of schizophrenia and suggest that opposite alterations in the pHVA or pMHPG levels may reflect specific changes in noradrenergic and dopaminergic functions in these deficit patients.

摘要

背景

精神分裂症阴性症状生化研究中的差异可能归因于缺乏对原发性和继发性阴性症状的区分。我们采用卡彭特标准将精神分裂症的缺陷综合征定义为存在持久的原发性阴性症状,并比较了缺陷型与非缺陷型精神分裂症患者的儿茶酚胺能参数。

方法

我们调查了34例接受抗精神病药物治疗的DSM-III-R精神分裂症患者的血浆高香草酸(pHVA)和3-甲氧基-4-羟基苯乙二醇(pMHPG)浓度,这些患者被分为缺陷型(n = 14)和非缺陷型(n = 20)精神分裂症。所有这些患者在之前的12个月中临床和治疗状态稳定。

结果

与20例非缺陷型精神分裂症患者相比,14例缺陷型精神分裂症患者在上午9点至12点的血浆pHVA水平较低,血浆pMHPG浓度较高。两组在任何人口统计学、治疗或临床变量上均无差异。

结论

我们的数据与精神分裂症缺陷综合征假定的不同病理生理基础一致,并表明pHVA或pMHPG水平的相反变化可能反映了这些缺陷患者去甲肾上腺素能和多巴胺能功能的特定变化。

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