Qi Wei, Blessing Esther, Li Chenxiang, Ardekani Babak A, Hart Kamber L, Marx Julia, Freudenreich Oliver, Cather Corinne, Holt Daphne, Bello Iruma, Diminich Erica D, Tang Yingying, Worthington Michelle, Zeng Botao, Wu Renrong, Fan Xiaoduo, Troxel Andrea, Zhao Jingping, Wang Jijun, Goff Donald C
Department of Psychiatry, NYU Langone Health, 1 Park Avenue, New York, NY 10016, United States of America.
Division of Biostatistics, Department of Population Health, NYU School of Medicine, 180 Madison Avenue, New York, NY 10016, United States of America.
Psychiatry Res Neuroimaging. 2021 Jun 30;312:111286. doi: 10.1016/j.pscychresns.2021.111286. Epub 2021 Apr 7.
Hippocampal volume loss is prominent in first episode schizophrenia (FES) and has been associated with poor clinical outcomes and with BDNF genotype; antidepressants are believed to reverse hippocampal volume loss via release of BDNF. In a 12-month, placebo-controlled add-on trial of the antidepressant, citalopram, during the maintenance phase of FES, negative symptoms were improved with citalopram. We now report results of structural brain imaging at baseline and 6 months in 63 FES patients (34 in citalopram group) from the trial to assess whether protection against hippocampal volume loss contributed to improved negative symptoms with citalopram. Hippocampal volumetric integrity (HVI) did not change significantly in the citalopram or placebo group and did not differ between treatment groups, whereas citalopram was associated with greater volume loss of the right CA1 subfield. Change in cortical thickness was associated with SANS change in 4 regions (left rostral anterior cingulate, right frontal pole, right cuneus, and right transverse temporal) but none differed between treatment groups. Our findings suggest that minimal hippocampal volume loss occurs after stabilization on antipsychotic treatment and that citalopram's potential benefit for negative symptoms is unlikely to result from protection against hippocampal volume loss or cortical thinning.
海马体体积缩小在首发精神分裂症(FES)中很突出,并且与不良临床结局以及脑源性神经营养因子(BDNF)基因型有关;抗抑郁药被认为可通过释放BDNF来逆转海马体体积缩小。在一项为期12个月、以安慰剂为对照的抗抑郁药西酞普兰在FES维持期的附加试验中,西酞普兰改善了阴性症状。我们现在报告该试验中63例FES患者(西酞普兰组34例)在基线和6个月时的脑结构成像结果,以评估防止海马体体积缩小是否有助于西酞普兰改善阴性症状。西酞普兰组或安慰剂组的海马体体积完整性(HVI)均未显著变化,且治疗组之间无差异,而西酞普兰与右侧CA1亚区更大的体积缩小有关。皮质厚度变化与4个区域(左侧喙前扣带回、右侧额极、右侧楔叶和右侧颞横回)的阴性症状评定量表(SANS)变化有关,但治疗组之间无差异。我们的研究结果表明,在抗精神病药物治疗稳定后,海马体体积缩小极少发生,并且西酞普兰对阴性症状的潜在益处不太可能源于防止海马体体积缩小或皮质变薄。