Department of Affective and Psychotic Disorders, Medical University of Lodz, Czechosłowacka 8/10, 92-216 Lodz, Poland.
Institute of Radioelectronics and Multimedia Technology, Warsaw University of Technology, Nowowiejska 15/19; 00-665 Warsaw, Poland.
Schizophr Res. 2018 May;195:168-175. doi: 10.1016/j.schres.2017.10.013. Epub 2017 Nov 2.
The aim of the study was to assess changes in cortical thickness related to the use of n-3 polyunsaturated fatty acids (PUFA) as add-on therapy in patients with first episode schizophrenia. A double-blind randomized controlled study was conducted using a 26-week intervention composed of concentrated fish oil containing 2.2g/d of eicosapentaenoic (EPA) and docosahexaenoic acid (DHA) or placebo (olive oil). Participants underwent MRI scanning twice to assess changes in cortical thickness: at the beginning and at the end of intervention. Data of suitable quality was obtained from 29 participants. The T1-weighted images for each participant were analyzed using FreeSurfer methodology for longitudinal pipeline. Significant differences in cortical thickness loss were observed between the groups in the parieto-occipital regions of Brodmann areas 7 and 19 of the left hemisphere, dysfunctions in which may be involved in schizophrenia symptomatology. The results of the study support the previous observations carried out in older individuals and patients with mild cognitive impairment, indicating that n-3 PUFA may have neuroprotective properties, especially at early stages of neurodegenerative diseases, such as schizophrenia. If replicated, the results of the present study may encourage clinicians to consider n-3 PUFA as a promising addition to antipsychotics for long-term treatment of schizophrenia.
本研究旨在评估作为附加治疗在首发精神分裂症患者中使用 n-3 多不饱和脂肪酸(PUFA)的情况下皮质厚度的变化。采用包含 2.2g/d 二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的浓缩鱼油或安慰剂(橄榄油)的 26 周干预进行了一项双盲随机对照研究。参与者接受了两次 MRI 扫描以评估皮质厚度的变化:干预开始时和结束时。从 29 名参与者中获得了质量合适的数据。使用 FreeSurfer 方法对每个参与者的 T1 加权图像进行了分析,用于纵向管道。在左侧大脑半球的 Brodmann 区域 7 和 19 的顶枕区域观察到组间皮质厚度损失的显著差异,这些区域的功能障碍可能与精神分裂症的症状学有关。该研究的结果支持在老年人和轻度认知障碍患者中进行的先前观察,表明 n-3 PUFA 可能具有神经保护特性,特别是在神经退行性疾病的早期阶段,如精神分裂症。如果得到复制,本研究的结果可能会鼓励临床医生考虑将 n-3 PUFA 作为抗精神病药物的一种有前途的附加治疗,用于精神分裂症的长期治疗。