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阿立哌唑与首发精神分裂症维持治疗期间海马萎缩减少的相关性。

Association of Aripiprazole With Reduced Hippocampal Atrophy During Maintenance Treatment of First-Episode Schizophrenia.

机构信息

From the Department of Psychiatry, NYU Langone Health, New York.

Division of Biostatistics, Department of Population Health, NYU School of Medicine, New York, NY.

出版信息

J Clin Psychopharmacol. 2021;41(3):244-249. doi: 10.1097/JCP.0000000000001391.

Abstract

PURPOSE/BACKGROUND: Hippocampal volume loss in early schizophrenia has been linked with markers of inflammation and oxidative stress, and with less response of negative symptoms. Aripiprazole has been reported to preserve hippocampal volume and to reduce inflammation.

METHODS/PROCEDURES: Study 1 was a 12-month multicenter randomized placebo-controlled trial of citalopram added to clinician-determined second-generation antipsychotic medication in 95 patients with first-episode schizophrenia (FES), 19 of whom received aripiprazole. We compared participants taking aripiprazole with those on other antipsychotics to determine whether those on aripiprazole had less hippocampal volume loss. We also examined peripheral biomarker data from medication-naive patients with schizophrenia receiving 8 weeks of antipsychotic treatment (n = 24) to see whether markers of inflammation and oxidative stress that previously predicted hippocampal volume differed between aripiprazole (n = 9) and other antipsychotics (study 2).

FINDINGS/RESULTS: Aripiprazole was associated with a mean increase in hippocampal volume of 0.35% (SD, 0.80%) compared with a 0.53% decrease (SD, 1.2%) with other antipsychotics during the first year of maintenance treatment in patients with FES. This difference was significant after adjusting for age, sex, citalopram treatment, and baseline Brief Psychiatric Rating Scale score (B = 0.0079, P = 0.03). Aripiprazole was also associated with reduced concentrations of the inflammatory cytokines interleukin-8 and tumor necrosis factor (P < 0.01) during the first 8 weeks of treatment in medication-naive patients with FES.

IMPLICATIONS/CONCLUSIONS: These results suggest that aripiprazole may protect against hippocampal atrophy via an anti-inflammatory mechanism, but these results require replication in larger, randomized trials, and the clinical relevance of hippocampal volume loss is not established.

摘要

目的/背景:早期精神分裂症中海马体积的损失与炎症和氧化应激的标志物有关,与阴性症状的反应较少有关。已有报道称阿立哌唑可保持海马体积并减少炎症。

方法/过程:研究 1 是一项为期 12 个月的多中心随机安慰剂对照试验,共纳入 95 名首发精神分裂症(FES)患者,他们在临床医生确定的第二代抗精神病药物基础上加用西酞普兰治疗,其中 19 名患者接受阿立哌唑治疗。我们比较了服用阿立哌唑和其他抗精神病药物的患者,以确定服用阿立哌唑的患者海马体积减少是否较少。我们还检查了接受 8 周抗精神病治疗的未经药物治疗的精神分裂症患者的外周生物标志物数据(n=24),以观察炎症和氧化应激标志物是否在阿立哌唑(n=9)和其他抗精神病药物(研究 2)之间存在差异。

结果/发现:在 FES 患者接受维持治疗的第一年中,阿立哌唑组海马体积平均增加 0.35%(SD,0.80%),而其他抗精神病药物组则减少 0.53%(SD,1.2%)。调整年龄、性别、西酞普兰治疗和基线简明精神病评定量表(BPRS)评分后,差异具有统计学意义(B=0.0079,P=0.03)。在未经药物治疗的 FES 患者中,阿立哌唑还与炎症细胞因子白细胞介素-8 和肿瘤坏死因子的浓度降低相关(P<0.01)。

结论/意义:这些结果表明,阿立哌唑可能通过抗炎机制预防海马萎缩,但这些结果需要在更大的随机试验中得到复制,并且海马体积减少的临床相关性尚未确定。

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