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首发精神分裂症的地塞米松抑制试验

Dexamethasone suppression test in first-episode schizophrenia.

作者信息

Cesková Eva, Kaspárek Tomás, Zourková Alexandra, Prikryl Radovan

机构信息

Department of Psychiatry, Masaryk University, Faculty of Medicine, Brno, Czech Republic.

出版信息

Neuro Endocrinol Lett. 2006 Aug;27(4):433-7.

Abstract

OBJECTIVES

Higher rates of dexamethasone test (DST) nonsuppression in schizophrenia have been attributed to depressive symptoms, suicidality and negative symptoms. No study concerning first-episode schizophrenia has yet been published.

DESIGN

In patients hospitalised for the first time with first-episode schizophrenia the DST has been performed before, at the end of the acute treatment and after one year. At the same time the clinical evaluation with PANSS was performed. A cortisol value >5 microgram/dl in either of the postdexamethasone samples indicated nonsuppression of cortisol.

RESULTS

A total of 56 males were included. 18% of pts were DST nonsuppressors at medication-free baseline, 5% and 16% after acute treatment and after one year respectively. After 1 year 42/56 of patients fulfilled the criteria of remission. The rate of nonsuppression was 21.4%, 5% and 16.4% in remitters and 7%, 7% and 14.3% in nonremitters. Significant differences in the whole group were found between postdexamethasone cortisolemia at discharge on the one hand and on admission and at the one-year follow-up on the other. Significant correlations were observed between postdexamethasone cortisolemia and negative symptoms at the end of acute treatment.

MAIN FINDINGS

In first-episode schizophrenia the short-term treatment led to a decrease in cortisolemia and rates of nonsuppression and an increase at a one-year follow-up.

CONCLUSIONS

Rates of DST nonsuppression in schizophrenia including first-episode schizophrenia are influenced by the stage of illness and medication status. The impairment of feedback regulation of cortisol secretion may be related to different biopathogenetic mechanisms depending on the phase of the illness.

摘要

目的

精神分裂症患者地塞米松试验(DST)不被抑制的发生率较高,这被归因于抑郁症状、自杀倾向和阴性症状。尚无关于首发精神分裂症的研究发表。

设计

对首次因首发精神分裂症住院的患者,在急性治疗前、急性治疗结束时及1年后进行了DST。同时用阳性和阴性症状量表(PANSS)进行临床评估。地塞米松给药后样本中皮质醇值>5微克/分升表明皮质醇未被抑制。

结果

共纳入56名男性患者。18%的患者在无药物基线时DST不被抑制,急性治疗后及1年后分别为5%和16%。1年后,56名患者中有42名达到缓解标准。缓解者中不被抑制的发生率分别为21.4%、5%和16.4%,未缓解者中分别为7%、7%和14.3%。在整个研究组中,出院时地塞米松给药后的皮质醇血症与入院时及1年随访时存在显著差异。在急性治疗结束时,观察到地塞米松给药后的皮质醇血症与阴性症状之间存在显著相关性。

主要发现

在首发精神分裂症中,短期治疗导致皮质醇血症和不被抑制率降低,而在1年随访时增加。

结论

包括首发精神分裂症在内的精神分裂症患者DST不被抑制的发生率受疾病阶段和用药状态影响。皮质醇分泌反馈调节的损害可能与疾病不同阶段的不同生物发病机制有关。

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