Nørbak-Emig Henrik, Ebdrup Bjørn H, Fagerlund Birgitte, Svarer Claus, Rasmussen Hans, Friberg Lars, Allerup Peter N, Rostrup Egill, Pinborg Lars H, Glenthøj Birte Y
Center for Neuropsychiatric Schizophrenia Research & Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Copenhagen University Hospital, Mental Health Centre Glostrup, Mental Health Services, Capital Region of Denmark, Glostrup, Denmark (Drs Nørbak-Emig, Ebdrup, Fagerlund, Rasmussen, and Glenthøj); University of Copenhagen, Faculty of Health and Medical Sciences, Department of Clinical Medicine, Copenhagen, Denmark (Drs Nørbak-Emig and Glenthøj); Neurobiology Research Unit and Epilepsy Clinic, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark (Drs Svarer and Pinborg); Department of Education, Centre for Research in Compulsory Schooling, Aarhus University, Denmark (Dr Allerup); Functional Imaging Unit, Department of Diagnostics, Copenhagen University Hospital, Glostrup Hospital, Denmark (Dr Rostrup); Department of Clinical Physiology and Nuclear Medicine, Copenhagen University, Bispebjerg Hospital, Denmark (Dr Friberg).
Int J Neuropsychopharmacol. 2016 Apr 29;19(5). doi: 10.1093/ijnp/pyw006. Print 2016 May.
We have previously reported associations between frontal D2/3 receptor binding potential positive symptoms and cognitive deficits in antipsychotic-naïve schizophrenia patients. Here, we examined the effect of dopamine D2/3 receptor blockade on cognition. Additionally, we explored the relation between frontal D2/3 receptor availability and treatment effect on positive symptoms.
Twenty-five antipsychotic-naïve first-episode schizophrenia patients were examined with the Positive and Negative Syndrome Scale, tested with the cognitive test battery Cambridge Neuropsychological Test Automated Battery, scanned with single-photon emission computerized tomography using the dopamine D2/3 receptor ligand [(123)I]epidepride, and scanned with MRI. After 3 months of treatment with either risperidone (n=13) or zuclopenthixol (n=9), 22 patients were reexamined.
Blockade of extrastriatal dopamine D2/3 receptors was correlated with decreased attentional focus (r = -0.615, P=.003) and planning time (r = -0.436, P=.048). Moreover, baseline frontal dopamine D2/3 binding potential and positive symptom reduction correlated positively (D2/3 receptor binding potential left frontal cortex rho = 0.56, P=.003; D2/3 receptor binding potential right frontal cortex rho = 0.48, P=.016).
Our data support the hypothesis of a negative influence of D2/3 receptor blockade on specific cognitive functions in schizophrenia. This is highly clinically relevant given the well-established association between severity of cognitive disturbances and a poor functional outcome in schizophrenia. Additionally, the findings support associations between frontal D2/3 receptor binding potential at baseline and the effect of antipsychotic treatment on positive symptoms.
我们之前报道过,在未服用抗精神病药物的精神分裂症患者中,额叶 D2/3 受体结合潜能与阳性症状及认知缺陷之间存在关联。在此,我们研究了多巴胺 D2/3 受体阻断对认知的影响。此外,我们探讨了额叶 D2/3 受体可用性与阳性症状治疗效果之间的关系。
对 25 名未服用抗精神病药物的首发精神分裂症患者进行阳性和阴性症状量表检查,使用剑桥神经心理测试自动成套测验进行认知测试,使用多巴胺 D2/3 受体配体[(123)I]表哌立酮进行单光子发射计算机断层扫描,并进行磁共振成像扫描。在用利培酮(n = 13)或氯普噻吨(n = 9)治疗 3 个月后,对 22 名患者进行复查。
纹状体外多巴胺 D2/3 受体阻断与注意力集中程度降低(r = -0.615,P = 0.003)和计划时间缩短(r = -0.436,P = 0.048)相关。此外,基线额叶多巴胺 D2/3 结合潜能与阳性症状减轻呈正相关(左额叶皮质 D2/3 受体结合潜能 rho = 0.56,P = 0.003;右额叶皮质 D2/3 受体结合潜能 rho = 0.48,P = 0.016)。
我们的数据支持 D2/3 受体阻断对精神分裂症特定认知功能有负面影响这一假设。鉴于认知障碍严重程度与精神分裂症功能预后不良之间已确立的关联,这在临床上具有高度相关性。此外,研究结果支持基线时额叶 D2/3 受体结合潜能与抗精神病药物治疗对阳性症状的效果之间存在关联。