Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, Centro de Investigación Biomédica en Red de Salud Mental, CIBERSAM, Madrid, Spain.
Schizophr Res. 2012 May;137(1-3):58-65. doi: 10.1016/j.schres.2012.01.040. Epub 2012 Feb 23.
Progressive loss of cortical gray matter (GM), as measured by magnetic resonance imaging, has been described early in the course of first-episode psychosis. This study aims to assess the relationship between oxidative balance and progression of cortical GM changes in a multicenter sample of first-episode early-onset psychosis (EOP) patients from baseline to two-year follow-up. A total of 48 patients (13 females, mean age 15.9±1.5 years) and 56 age- and gender-matched healthy controls (19 females, 15.3±1.5 years) were assessed. Magnetic resonance imaging (MRI) scans performed both at the time of the first psychotic episode and 2 years later were used for volumetric measurements of left and right gray matter regions (frontal, parietal, and temporal lobes) and total sulcal cerebrospinal fluid (CSF). Total glutathione (GSH) blood levels were determined at baseline. In patients, after controlling for possible confounding variables, lower baseline GSH levels were significantly associated with greater volume decrease in left frontal (B=0.034, 95% confidence interval (CI): 0.011 to 0.056, r=0.620, p=0.006), parietal (B=0.039, 95% CI: 0.020 to 0.059, r=0.739, p=0.001), temporal (B=0.026, 95% CI: 0.016 to 0.036, r=0.779, p<0.001), and total (B=0.022, 95% CI: 0.014 to 0.031, r=0.803, p<0.001) gray matter, and with greater increase in total CSF (B=-0.560, 95% CI: -0.270 to -0.850, r=-0.722, p=0.001). Controls did not show significant associations between brain volume changes and GSH levels. GSH deficit during the first psychotic episode was related to greater loss of cortical GM two years later in patients with first-episode EOP, suggesting that oxidative damage may contribute to the progressive loss of cortical GM found in patients with first-episode psychosis.
皮质灰质(GM)的进行性损失,通过磁共振成像测量,在首发精神病的病程早期就已经描述过。本研究旨在评估在首发早发性精神病(EOP)患者的多中心样本中,氧化平衡与皮质 GM 变化进展之间的关系,这些患者从基线到两年随访进行了评估。共评估了 48 名患者(13 名女性,平均年龄 15.9±1.5 岁)和 56 名年龄和性别匹配的健康对照者(19 名女性,15.3±1.5 岁)。在首次精神病发作时和 2 年后均进行磁共振成像(MRI)扫描,用于测量左侧和右侧灰质区域(额叶、顶叶和颞叶)和总脑沟脑脊液(CSF)的容积。在基线时测定总谷胱甘肽(GSH)的血液水平。在患者中,在控制了可能的混杂变量后,较低的基线 GSH 水平与左侧额(B=0.034,95%置信区间(CI):0.011 至 0.056,r=0.620,p=0.006)、顶(B=0.039,95% CI:0.020 至 0.059,r=0.739,p=0.001)、颞(B=0.026,95% CI:0.016 至 0.036,r=0.779,p<0.001)和总(B=0.022,95% CI:0.014 至 0.031,r=0.803,p<0.001)灰质体积减少显著相关,与总 CSF 增加显著相关(B=-0.560,95% CI:-0.270 至-0.850,r=-0.722,p=0.001)。对照者未显示脑体积变化与 GSH 水平之间的显著相关性。首发精神病发作期间的 GSH 不足与两年后首发 EOP 患者皮质 GM 的更大损失有关,这表明氧化损伤可能导致首发精神病患者中发现的皮质 GM 进行性丧失。