Tuozzo Carissa, Lyall Amanda E, Pasternak Ofer, James Anthony C D, Crow Timothy J, Kubicki Marek
Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Bipolar Disord. 2018 Sep;20(6):523-530. doi: 10.1111/bdi.12588. Epub 2017 Dec 11.
Bipolar disorder (BP) is a debilitating psychiatric disease that is not well understood. Previous diffusion magnetic resonance imaging (dMRI) studies of BP patients found prominent microstructural white matter (WM) abnormalities of reduced fractional anisotropy (FA). Because FA is a nonspecific measure, relating these abnormalities to a specific pathology is difficult. Here, dMRI specificity was increased by free water (FW) imaging, which allows identification of changes in extracellular space (FW) from neuronal tissue (fractional anisotropy of tissue [FA-t]). Previous studies identified increased FW in early schizophrenia (SZ) stages which was replaced by widespread decreased FA-t in chronic stages. This is the first analysis utilizing this method to compare BP patients and controls.
3 Tesla diffusion weighted imaging (3T DWI) data were acquired for 17 chronic BP and 28 healthy control (HC) participants at Oxford University. Tract-based spatial statistics was utilized to generate a WM skeleton. FW imaging deconstructed the diffusion signal into extracellular FW and tissue FA-t maps. These maps were projected onto the skeleton and FA, FA-t, and FW were compared between groups.
We found significantly lower FA in BP patients when compared to HC in areas that overlapped with extensive FW increases. There were no FA-t differences.
Our study suggests that chronic BP shows similar WM changes to early SZ, suggesting that extracellular FW increases could be a transient indication of recent psychotic episodes. Since FW increase in SZ has been suggested to be related to neuroinflammation, we theorize that neuroinflammation might be a shared pathology between chronic BP and early SZ.
双相情感障碍(BP)是一种使人衰弱的精神疾病,目前人们对其了解并不充分。先前对双相情感障碍患者进行的扩散磁共振成像(dMRI)研究发现,其显著的微观结构白质(WM)异常表现为分数各向异性(FA)降低。由于FA是一种非特异性测量指标,因此很难将这些异常与特定病理联系起来。在这里,通过自由水(FW)成像提高了dMRI的特异性,该成像能够从神经元组织(组织分数各向异性[FA-t])中识别细胞外间隙(FW)的变化。先前的研究发现,精神分裂症(SZ)早期阶段FW增加,而在慢性阶段则被广泛的FA-t降低所取代。这是首次利用这种方法对双相情感障碍患者和对照组进行比较的分析。
在牛津大学,对17名慢性双相情感障碍患者和28名健康对照(HC)参与者采集了3特斯拉扩散加权成像(3T DWI)数据。利用基于纤维束的空间统计学方法生成白质骨架。FW成像将扩散信号解构为细胞外FW和组织FA-t图。将这些图投影到骨架上,并比较两组之间的FA、FA-t和FW。
与健康对照相比,双相情感障碍患者在与广泛的FW增加重叠的区域中FA显著降低。FA-t没有差异。
我们的研究表明,慢性双相情感障碍表现出与精神分裂症早期相似的白质变化,这表明细胞外FW增加可能是近期精神病发作的一个短暂指标。由于精神分裂症中FW增加被认为与神经炎症有关,我们推测神经炎症可能是慢性双相情感障碍和精神分裂症早期的共同病理。