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首发精神病患者抗精神病药物和疾病对脑容量减少影响的鉴别:一项纵向、随机、三盲、安慰剂对照 MRI 研究。

Differentiating the effect of antipsychotic medication and illness on brain volume reductions in first-episode psychosis: A Longitudinal, Randomised, Triple-blind, Placebo-controlled MRI Study.

机构信息

Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, VIC, Australia.

Monash Biomedical Imaging, Monash University, Clayton, VIC, Australia.

出版信息

Neuropsychopharmacology. 2021 Jul;46(8):1494-1501. doi: 10.1038/s41386-021-00980-0. Epub 2021 Feb 26.

Abstract

Changes in brain volume are a common finding in Magnetic Resonance Imaging (MRI) studies of people with psychosis and numerous longitudinal studies suggest that volume deficits progress with illness duration. However, a major unresolved question concerns whether these changes are driven by the underlying illness or represent iatrogenic effects of antipsychotic medication. In this study, 62 antipsychotic-naïve patients with first-episode psychosis (FEP) received either a second-generation antipsychotic (risperidone or paliperidone) or a placebo pill over a treatment period of 6 months. Both FEP groups received intensive psychosocial therapy. A healthy control group (n = 27) was also recruited. Structural MRI scans were obtained at baseline, 3 months and 12 months. Our primary aim was to differentiate illness-related brain volume changes from medication-related changes within the first 3 months of treatment. We secondarily investigated long-term effects at the 12-month timepoint. From baseline to 3 months, we observed a significant group x time interaction in the pallidum (p < 0.05 FWE-corrected), such that patients receiving antipsychotic medication showed increased volume, patients on placebo showed decreased volume, and healthy controls showed no change. Across the entire patient sample, a greater increase in pallidal grey matter volume over 3 months was associated with a greater reduction in symptom severity. Our findings indicate that psychotic illness and antipsychotic exposure exert distinct and spatially distributed effects on brain volume. Our results align with prior work in suggesting that the therapeutic efficacy of antipsychotic medications may be primarily mediated through their effects on the basal ganglia.

摘要

脑容量变化是精神分裂症患者磁共振成像(MRI)研究中的常见发现,许多纵向研究表明,体积缺陷随疾病持续时间而进展。然而,一个尚未解决的主要问题是这些变化是由潜在疾病驱动的,还是抗精神病药物的医源性影响。在这项研究中,62 名首次发作精神分裂症(FEP)的抗精神病药物初治患者接受了第二代抗精神病药物(利培酮或帕利哌酮)或安慰剂治疗 6 个月。两组 FEP 患者均接受了强化心理社会治疗。还招募了一个健康对照组(n=27)。在基线、3 个月和 12 个月时进行了结构 MRI 扫描。我们的主要目的是区分治疗前 3 个月内与疾病相关的脑容量变化与与药物相关的变化。我们还在 12 个月的时间点上研究了长期影响。从基线到 3 个月,我们观察到苍白球存在显著的组 x 时间交互作用(p<0.05,FWE 校正),即接受抗精神病药物治疗的患者体积增加,接受安慰剂的患者体积减少,健康对照组没有变化。在整个患者样本中,3 个月内苍白球灰质体积增加越大,症状严重程度降低越大。我们的发现表明,精神疾病和抗精神病药物暴露对脑容量产生了独特且空间分布的影响。我们的结果与先前的工作一致,表明抗精神病药物的治疗效果可能主要通过其对基底节的影响来介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb5b/8209146/f1fb1f08e9bd/41386_2021_980_Fig1_HTML.jpg

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