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首页> 外文期刊>Frontiers in Neuropharmacology >Striatal Volume Increase After Six Weeks of Selective Dopamine D2/3 Receptor Blockade in First-Episode, Antipsychotic-Na?ve Schizophrenia Patients
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Striatal Volume Increase After Six Weeks of Selective Dopamine D2/3 Receptor Blockade in First-Episode, Antipsychotic-Na?ve Schizophrenia Patients

机译:在第一集集中的选择性多巴胺D2 / 3受体阻断后六周后,纹纹体积增加,抗精神病药患者

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Patients with chronic schizophrenia often display enlarged striatal volumes, and antipsychotic drugs may contribute via the dopamine D2/3 receptor (D2/3R) blockade. Separating the effects of disease from medication is challenging due to the lack of a proper placebo-group. To address this, we conducted a longitudinal study of antipsychotic-na?ve, first-episode schizophrenia patients to test the hypothesis that selective blockade of D2/3R would induce a dose-dependent striatal volume increase. Twenty-one patients underwent structural magnetic resonance imaging (sMRI), single-photon emission computed tomography (SPECT), and symptom severity ratings before and after six weeks of amisulpride treatment. Twenty-three matched healthy controls underwent sMRI and baseline SPECT. Data were analyzed using repeated measures and multiple regression analyses. Correlations between symptom severity decrease, volume changes, dose and receptor occupancy were explored. Striatal volumes did not differ between patients and controls at baseline or follow-up, but a significant group-by-time interaction was found (p = 0.01). This interaction was explained by a significant striatal volume increase of 2.1% in patients (Cohens d = 0.45). Striatal increase was predicted by amisulpride dose, but not by either D2/3R occupancy or baseline symptom severity. A significant reduction in symptom severity was observed at a mean dose of 233.3 (SD = 109.9) mg, corresponding to D2/3R occupancy of 44.65%. Reduction in positive symptoms correlated significantly with striatal volume increase, driven by reductions in hallucinations. Our data demonstrate a clear link between antipsychotic treatment and striatal volume increase in antipsychotic-na?ve schizophrenia patients. Moreover, the treatment-induced striatal volume increase appears clinically relevant by correlating to reductions in core symptoms of schizophrenia.
机译:慢性精神分裂症患者经常显示扩大的纹状体体积,并且抗精神病药物可能通过多巴胺D2 / 3受体(D2 / 3R)阻断有助于延迟。由于缺乏适当的安慰剂组,将疾病的影响与药物分开是挑战。为了解决这一点,我们进行了对抗精神病药症的纵向研究,首发精神分裂症患者进行测试,以测试D2 / 3R的选择性阻滞的假设会诱导剂量依赖性纹体体积增加。二十一名患者接受了结构磁共振成像(SMRI),单光子发射计算断层扫描(SPECT),以及六周的氨基丙烯处理前后的症状严重程度评级。二十三个匹配的健康控制接受了SMRI和基线SPECT。使用重复措施和多元回归分析进行分析数据。探讨了症状严重程度之间的相关性,体积变化,剂量和受体占用。基线或随访的患者和对照之间的纹纹体积没有差异,但发现了显着的逐次相互作用(P = 0.01)。这种相互作用是通过显着的薄膜体积增加2.1%(Cohens D = 0.45)解释。由氨基普雷德剂量预测纹纹纹状体,但不是D2 / 3R占状或基线症状严重程度。在233.3(SD = 109.9)Mg的平均剂量的平均剂量下观察到症状严重程度的显着降低,对应于44.65%的D2 / 3R占状。阳性症状的减少显着与纹状体增加显着,通过幻觉的减少驱动。我们的数据显示了抗精神病药治疗和抗精神病药患者抗精神病药物的综合链接。此外,通过与精神分裂症的核心症状的减少相关,临床相关的治疗诱导的纹状体积增加。

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