Yamanashi Prefectural Kita Hospital, Yamanashi, Japan; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Yamanashi Prefectural Kita Hospital, Yamanashi, Japan.
Prog Neuropsychopharmacol Biol Psychiatry. 2020 Jan 10;96:109756. doi: 10.1016/j.pnpbp.2019.109756. Epub 2019 Aug 28.
This systematic review aimed to elucidate the relationship between polydipsia and antipsychotics.
We systematically searched MEDLINE, Embase, and PsycINFO, and included clinical studies and case reports on polydipsia induced or improved by antipsychotics.
We identified 61 articles: 1 double-blind randomized controlled trial (RCT), 4 single-arm trials, 1 cross-sectional study, 3 case series, and 52 case reports. The double-blind RCT demonstrated no significant difference in improvement in polydipsia between olanzapine and haloperidol. Two single-arm trials showed that polydipsia improved during clozapine treatment, whereas the other 2 showed that risperidone did not improve polydipsia. The cross-sectional study showed the prevalence of hyponatremia with first-generation antipsychotics (FGAs: 26.1%) and second-generation antipsychotics (SGAs: 4.9%). Two case series reported that clozapine improved polydipsia; the other one indicated that patients with polydipsia who were treated with FGAs had schizophrenia (70.4%) and mental retardation (25.9%). Of 90 cases in the case reports, 67 (75.3%) were diagnosed with schizophrenia. Of 83 cases in which antipsychotic treatment started before the onset of polydipsia, 75 (90.3%) received FGAs, particularly haloperidol (n = 24, 28.9%), and 11 (13.3%) received risperidone. Among 40 cases in which polydipsia was improved following antipsychotic treatment, 36 (90.0%) received SGAs, primarily clozapine (n = 14, 35.0%).
Although the causal relationship between polydipsia and antipsychotics remains unclear because of the paucity of high-quality studies, antipsychotics with high affinity to dopamine D receptors may be associated with an increased risk of polydipsia while clozapine may be effective for treating polydipsia.
本系统评价旨在阐明多饮与抗精神病药之间的关系。
我们系统地检索了 MEDLINE、Embase 和 PsycINFO,并纳入了关于抗精神病药引起或改善多饮的临床研究和病例报告。
我们共确定了 61 篇文章:1 项双盲随机对照试验(RCT)、4 项单臂试验、1 项横断面研究、3 项病例系列研究和 52 项病例报告。双盲 RCT 表明奥氮平和氟哌啶醇在改善多饮方面无显著差异。2 项单臂试验表明氯氮平治疗期间多饮改善,而另外 2 项试验表明利培酮不能改善多饮。横断面研究显示第一代抗精神病药(FGAs:26.1%)和第二代抗精神病药(SGAs:4.9%)存在低钠血症的患病率。2 项病例系列报告氯氮平改善了多饮;另一个病例表明,用 FGAs 治疗的多饮患者患有精神分裂症(70.4%)和智力迟钝(25.9%)。在病例报告中的 90 例中,67 例(75.3%)被诊断为精神分裂症。在多饮发生前开始抗精神病药物治疗的 83 例中,75 例(90.3%)接受 FGAs,特别是氟哌啶醇(n=24,28.9%),11 例(13.3%)接受利培酮。在 40 例抗精神病药物治疗后多饮改善的病例中,36 例(90.0%)接受 SGAs,主要是氯氮平(n=14,35.0%)。
尽管由于高质量研究的缺乏,多饮与抗精神病药之间的因果关系尚不清楚,但多巴胺 D 受体亲和力高的抗精神病药可能与多饮风险增加相关,而氯氮平可能对治疗多饮有效。