首页> 美国卫生研究院文献>Neuropsychiatric Disease and Treatment >The effects of additional treatment with terguride a partial dopamine agonist on hyperprolactinemia induced by antipsychotics in schizophrenia patients: a preliminary study
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The effects of additional treatment with terguride a partial dopamine agonist on hyperprolactinemia induced by antipsychotics in schizophrenia patients: a preliminary study

机译:初步研究表明多巴胺激动剂terguride对精神分裂症患者抗精神病药引起的高泌乳素血症的影响:初步研究

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摘要

Hyperprolactinemia is a frequent consequence of treatment with antipsychotics. Earlier studies have indicated that terguride, which is a partial dopamine agonist, reduces the prolactin levels that are induced by prolactinemia. Thus, we examined the dose effects of adjunctive treatment with terguride on the plasma concentrations of prolactin in patients with elevated prolactin levels resulting from antipsychotic treatment. Terguride was concomitantly administered to 20 schizophrenic patients (10 males and 10 females) receiving paliperidone and risperidone. The dose of terguride was 1.0 mg/day. Sample collections for prolactin were conducted before terguride (baseline) and 2–4 weeks after administration. The samples were obtained after the morning dose of terguride. The average (± standard deviation) plasma prolactin concentration during terguride coadministration was significantly lower than the baseline concentration in females (82.3±37.1 ng/mL versus 56.5±28.5 ng/mL, P<0.01) but not in males (28.8±18.0 ng/mL versus 26.2±13.1 ng/mL, not significant). Additionally, a significant correlation between the ratio of prolactin reduction and the baseline prolactin concentration was identified in males (rs=−0.638, P<0.05) but not in females (rs=−0.152, not significant). Many patients complained of various adverse events following terguride administration, such as insomnia, agitation, and/or the aggravation of hallucinations. This study suggests that additional treatment with terguride decreases the prolactin concentrations in females experiencing high prolactin levels as a result of antipsychotic treatment. However, its utility for schizophrenia may be diminished because of its low tolerability.
机译:高催乳素血症是抗精神病药治疗的常见结果。较早的研究表明,作为部分多巴胺激动剂的terguride可以降低由催乳素血症引起的催乳素水平。因此,在由抗精神病药物治疗导致催乳素水平升高的患者中,我们检查了特格列特辅助治疗对催乳素血浆浓度的剂量影响。特格瑞特同时给予接受帕潘立酮和利培酮治疗的20例精神分裂症患者(男性10例,女性10例)服用。特固利的剂量为1.0毫克/天。催乳素的样品收集是在特屈利特(基线)之前和给药后2-4周进行的。早晨服用特格列脲后获得样品。特格列特联合用药期间的平均血浆催乳素浓度(±标准偏差)显着低于女性的基线浓度(82.3±37.1 ng / mL对比56.5±28.5 ng / mL,P <0.01),但男性没有(28.8±18.0 ng) / mL对比26.2±13.1 ng / mL,无显着性)。此外,在男性(rs = -0.638,P <0.05)中发现催乳素减少率与基线催乳素浓度之间存在显着相关性,而在女性中则没有(rs = -0.152,不显着)。许多患者抱怨在使用特格瑞特后发生了各种不良事件,例如失眠,情绪激动和/或幻觉加剧。这项研究表明,由于抗精神病药物的治疗,特格列特的额外治疗可降低患有高催乳素水平的女性的催乳素浓度。但是,由于它的低耐受性,它在精神分裂症中的效用可能会降低。

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