Sarıçiçek A, Zorlu N, Yalın N, Hıdıroğlu C, Çavuşoğlu B, Ceylan D, Ada E, Tunca Z, Özerdem A
Department of Psychiatry,Faculty of Medicine,Izmir Katip Celebi University,Ataturk Training and Research Hospital,Izmir,Turkey.
Department of Neuroscience,Health Sciences Institute,Dokuz Eylul University,Izmir,Turkey.
Psychol Med. 2016 May;46(7):1547-58. doi: 10.1017/S0033291716000180. Epub 2016 Mar 7.
Several lines of evidence suggest that bipolar disorder (BD) is associated with white matter (WM) pathology. Investigation of unaffected first-degree relatives of BD patients may help to distinguish structural biomarkers of genetic risk without the confounding effects of burden of illness, medication or clinical state. In the present study, we applied tract-based spatial statistics to study WM changes in patients with BD, unaffected siblings and controls.
A total of 27 euthymic patients with BD type I, 20 unaffected siblings of bipolar patients and 29 healthy controls who did not have any current or past diagnosis of Axis I psychiatric disorders were enrolled in the study.
Fractional anisotropy (FA) was significantly lower in BD patients than in the control group in the corpus callosum, fornix, bilateral superior longitudinal fasciculus, inferior longitudinal fasciculus, inferior fronto-occipital fasciculus, anterior thalamic radiation, posterior thalamic radiation, cingulum, uncinate fasciculus, superior corona radiata, anterior corona radiata and left external capsule. In region-of-interest (ROI) analyses, we found that both unaffected siblings and bipolar patients had significantly reduced FA in the left posterior thalamic radiation, the left sagittal stratum, and the fornix compared with healthy controls. Average FA for unaffected siblings was intermediate between the healthy controls and bipolar patients within these ROIs.
Decreased FA in the fornix, left posterior thalamic radiation and left sagittal stratum in both bipolar patients and unaffected siblings may represent a potential structural endophenotype or a trait-based marker for BD.
多项证据表明双相情感障碍(BD)与白质(WM)病变有关。对BD患者未受影响的一级亲属进行研究,可能有助于区分遗传风险的结构生物标志物,而不受疾病负担、药物治疗或临床状态的混杂影响。在本研究中,我们应用基于束的空间统计学方法来研究BD患者、未受影响的同胞以及对照组的白质变化。
本研究共纳入27例处于缓解期的I型BD患者、20例双相情感障碍患者的未受影响的同胞以及29名目前或既往均未被诊断为轴I精神障碍的健康对照者。
在胼胝体、穹窿、双侧上纵束、下纵束、额枕下束、丘脑前辐射、丘脑后辐射、扣带束、钩束、放射冠上部、放射冠前部以及左侧外囊,BD患者的各向异性分数(FA)显著低于对照组。在感兴趣区域(ROI)分析中,我们发现与健康对照相比,未受影响的同胞和双相情感障碍患者在左侧丘脑后辐射、左侧矢状层以及穹窿中的FA均显著降低。在这些ROI内,未受影响的同胞的平均FA处于健康对照和双相情感障碍患者之间。
双相情感障碍患者和未受影响的同胞在穹窿、左侧丘脑后辐射和左侧矢状层中FA降低,可能代表BD的潜在结构内表型或基于特质的标志物。