Ahmed Mohamed, Cannon Dara M, Scanlon Cathy, Holleran Laurena, Schmidt Heike, McFarland John, Langan Camilla, McCarthy Peter, Barker Gareth J, Hallahan Brian, McDonald Colm
Clinical Neuroimaging Laboratory, Department of Psychiatry, College of Medicine, Nursing and Health Sciences, National University of Ireland, Galway, Galway, Ireland.
Department of Radiology, College of Medicine, Nursing and Health Sciences, National University of Ireland, Galway, Galway, Ireland.
Neuropsychopharmacology. 2015 Sep;40(10):2409-17. doi: 10.1038/npp.2015.90. Epub 2015 Apr 1.
Despite evidence that clozapine may be neuroprotective, there are few longitudinal magnetic resonance imaging (MRI) studies that have specifically explored an association between commencement of clozapine treatment for schizophrenia and changes in regional brain volume or cortical thickness. A total of 33 patients with treatment-resistant schizophrenia and 31 healthy controls matched for age and gender underwent structural MRI brain scans at baseline and 6-9 months after commencing clozapine. MRI images were analyzed using SIENA (Structural Image Evaluation, using Normalization, of Atrophy) and FreeSurfer to investigate changes over time in brain volume and cortical thickness respectively. Significantly greater reductions in volume were detected in the right and left medial prefrontal cortex and in the periventricular area in the patient group regardless of treatment response. Widespread further cortical thinning was observed in patients compared with healthy controls. The majority of patients improved symptomatically and functionally over the study period, and patients who improved were more likely to have less cortical thinning of the left medial frontal cortex and the right middle temporal cortex. These findings demonstrate on-going reductions in brain volume and progressive cortical thinning in patients with schizophrenia who are switched to clozapine treatment. It is possible that this gray matter loss reflects a progressive disease process irrespective of medication use or that it is contributed to by switching to clozapine treatment. The clinical improvement of most patients indicates that antipsychotic-related gray matter volume loss may not necessarily be harmful or reflect neurotoxicity.
尽管有证据表明氯氮平可能具有神经保护作用,但很少有纵向磁共振成像(MRI)研究专门探讨氯氮平治疗精神分裂症的起始与脑区体积或皮质厚度变化之间的关联。共有33例难治性精神分裂症患者和31名年龄及性别匹配的健康对照在基线时以及开始使用氯氮平治疗6 - 9个月后接受了脑部结构MRI扫描。分别使用SIENA(基于萎缩归一化的结构图像评估)和FreeSurfer分析MRI图像,以研究脑体积和皮质厚度随时间的变化。无论治疗反应如何,患者组的左右内侧前额叶皮质和脑室周围区域的体积减少均显著更大。与健康对照相比,患者出现广泛的皮质进一步变薄。在研究期间,大多数患者的症状和功能有所改善,症状改善的患者更有可能左侧内侧额叶皮质和右侧颞中皮质的皮质变薄程度较小。这些发现表明,改用氯氮平治疗的精神分裂症患者脑体积持续减少且皮质逐渐变薄。这种灰质损失可能反映了一种与药物使用无关的进行性疾病过程,或者是由改用氯氮平治疗所致。大多数患者的临床改善表明,抗精神病药物相关的灰质体积减少不一定有害或反映神经毒性。