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性功能障碍与抗精神病药物治疗

Sexual dysfunction and antipsychotic treatment.

作者信息

Cutler A J

机构信息

Department of Psychiatry and Behavioral Medicine, University of South Florida, 807 West Morse Boulevard, Suite 101, Winter Park, FL 32789, USA.

出版信息

Psychoneuroendocrinology. 2003 Jan;28 Suppl 1:69-82. doi: 10.1016/s0306-4530(02)00113-0.

Abstract

Human sexual function is complex and affected in many different ways by schizophrenia and the antipsychotic drugs used in its treatment. The evaluation of the effects of antipsychotics on sexual function in patients with schizophrenia is also complex because the deleterious effects of conventional antipsychotics are superimposed on the effects of the disease itself. Although not extensively researched, sexual dysfunction seems to be frequent in patients with schizophrenia, especially in men. Sexual dysfunction appears, in significant part, to be a direct consequence of dopamine antagonism, combined with indirect effects due to increased serum prolactin concentration. Atypical antipsychotics have a number of potential advantages over standard agents with regard to their impact on sexual function. Clinical reports indicate that atypical antipsychotics are associated with a lower incidence of sexual adverse events than conventional antipsychotics and that there may also be important differences between them in this regard. For example, dose-related increases in prolactin concentrations occur with risperidone whereas olanzapine is associated with mild and transient increases in long-term treatment. Treatment with clozapine does not result in prolactin elevation and, like olanzapine, only transient increases occur with ziprasidone therapy, but the risk of agranulocytosis with clozapine restricts its use. Quetiapine has no more effect on serum prolactin than placebo across its full dose range. Together with its low frequency of reproductive or hormonal side effects and a low incidence of extrapyramidal symptoms, the tolerability profile of quetiapine may be particularly beneficial for many patients. Sexual dysfunction can be an important source of distress to patients and adversely affects compliance, and is one of the factors that must be taken into account when selecting treatment.

摘要

人类性功能很复杂,会受到精神分裂症及其治疗中使用的抗精神病药物多种不同方式的影响。评估抗精神病药物对精神分裂症患者性功能的影响也很复杂,因为传统抗精神病药物的有害作用叠加在疾病本身的影响之上。虽然研究并不广泛,但性功能障碍在精神分裂症患者中似乎很常见,尤其是男性。性功能障碍在很大程度上似乎是多巴胺拮抗作用的直接后果,再加上血清催乳素浓度升高产生的间接影响。非典型抗精神病药物在对性功能的影响方面比标准药物有一些潜在优势。临床报告表明,与传统抗精神病药物相比,非典型抗精神病药物引起性不良事件的发生率较低,而且在这方面它们之间可能也存在重要差异。例如,利培酮会导致催乳素浓度随剂量增加,而奥氮平在长期治疗中与轻度短暂升高有关。氯氮平治疗不会导致催乳素升高,齐拉西酮治疗也像奥氮平一样只会引起短暂升高,但氯氮平导致粒细胞缺乏症的风险限制了其使用。喹硫平在其整个剂量范围内对血清催乳素的影响不超过安慰剂。喹硫平的耐受性特征,连同其生殖或激素副作用频率低以及锥体外系症状发生率低,可能对许多患者特别有益。性功能障碍可能是患者痛苦的一个重要来源,对依从性有不利影响,并且是选择治疗时必须考虑的因素之一。

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