Department of Psychiatry, Stellenbosch University, Tygerberg Campus, Cape Town, South Africa.
Department of Psychiatry, Nelson R Mandela School of Medicine, University of Kwazulu-Natal, Durban, South Africa.
Psychol Med. 2023 Apr;53(5):2050-2059. doi: 10.1017/S0033291721003809. Epub 2021 Sep 23.
Progressive brain structural MRI changes are described in schizophrenia and have been ascribed to both illness progression and antipsychotic treatment. We investigated treatment effects, in terms of total cumulative antipsychotic dose, efficacy and tolerability, on brain structural changes over the first 24 months of treatment in schizophrenia.
A prospective, 24-month, single-site cohort study in 99 minimally treated patients with first-episode schizophrenia, schizophreniform and schizoaffective disorder, and 98 matched healthy controls. We treated the patients according to a fixed protocol with flupenthixol decanoate, a long-acting injectable antipsychotic. We assessed psychopathology, cognition, extrapyramidal symptoms and BMI, and acquired MRI scans at months 0, 12 and 24. We selected global cortical thickness, white matter volume and basal ganglia volume as the regions of interest.
The only significant group × time interaction was for basal ganglia volumes. However, patients, but not controls, displayed cortical thickness reductions and increases in white matter and basal ganglia volumes. Cortical thickness reductions were unrelated to treatment. White matter volume increases were associated with lower cumulative antipsychotic dose, greater improvements in psychopathology and cognition, and more extrapyramidal symptoms. Basal ganglia volume increases were associated with greater improvements in psychopathology, greater increases in BMI and more extrapyramidal symptoms.
We provide evidence for plasticity in white matter and basal ganglia associated with antipsychotic treatment in schizophrenia, most likely linked to the dopamine blocking actions of these agents. Cortical changes may be more closely related to the neurodevelopmental, non-dopaminergic aspects of the illness.
精神分裂症患者的大脑结构 MRI 呈现出进展性变化,这些变化被归因于疾病进展和抗精神病药物治疗。我们研究了治疗效果,即总累积抗精神病药物剂量、疗效和耐受性,对精神分裂症患者治疗最初 24 个月的大脑结构变化的影响。
一项为期 24 个月、单站点、前瞻性队列研究,纳入了 99 名首次发作的精神分裂症、分裂情感障碍和分裂样障碍的轻度治疗患者和 98 名匹配的健康对照者。我们根据固定方案用氟奋乃静葵酸酯(一种长效注射用抗精神病药物)治疗患者。我们评估了精神病理学、认知、锥体外系症状和 BMI,并在第 0、12 和 24 个月时获取 MRI 扫描。我们选择了全脑皮质厚度、白质体积和基底节体积作为感兴趣区。
唯一显著的组间时间交互作用是基底节体积。然而,只有患者而不是对照者表现出皮质厚度减少和白质及基底节体积增加。皮质厚度减少与治疗无关。白质体积增加与较低的累积抗精神病药物剂量、精神病理学和认知的改善更大以及锥体外系症状更多有关。基底节体积增加与精神病理学的改善更大、BMI 的增加更大以及锥体外系症状更多有关。
我们提供了精神分裂症中与抗精神病药物治疗相关的白质和基底节可塑性的证据,这很可能与这些药物的多巴胺阻断作用有关。皮质变化可能与疾病的神经发育、非多巴胺能方面更密切相关。