Psychiatric Centre Copenhagen, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Neuroimage Clin. 2017 Dec 7;17:786-793. doi: 10.1016/j.nicl.2017.12.011. eCollection 2018.
Major depression and bipolar disorders aggregates in families and are linked with a wide range of neurobiological abnormalities including cortical gray matter (GM) alterations. Prospective studies of individuals at familial risk may expose the neural mechanisms underlying risk transmission.
We used voxel based morphometry to investigate changes in regional GM brain volume, over a seven-year period, in 37 initially healthy individuals having a mono- or di-zygotic twin diagnosed with major depression or bipolar disorder (high-risk group; mean age 41.6 yrs.) as compared to 36 individuals with no history of affective disorders in the index twin and first-degree relatives (low-risk group; mean age 38.5 yrs.).
Groups did not differ in regional GM volume changes over time. However, independent of time, high-risk twins had significantly greater GM volumes in bilateral dorsal anterior cingulate, inferior frontal gyrus and temporoparietal regions as compared to low-risk twins. Further, individuals who developed an affective disorder at follow-up (n = 12), had relatively the largest GM volumes, both at baseline and follow-up, in the right dorsal anterior cingulate cortex and right inferior frontal cortex compared to high- and low-risk twins who remained well at follow-up.
This pattern of apparently stable grater regional GM volume may constitute a neural marker of an increased risk for developing an affective disorder in individuals at familial risk.
重度抑郁和双相情感障碍在家族中聚集,并与广泛的神经生物学异常相关,包括皮质灰质(GM)改变。对具有家族风险的个体进行前瞻性研究可能会揭示风险传递的神经机制。
我们使用基于体素的形态测量学方法,在 7 年的时间内,对 37 名最初健康的个体进行了研究,这些个体的单卵或双卵双胞胎被诊断患有重度抑郁或双相情感障碍(高风险组;平均年龄 41.6 岁),与 36 名指数双胞胎和一级亲属中没有情感障碍病史的个体(低风险组;平均年龄 38.5 岁)进行了比较。
两组在区域 GM 体积随时间的变化上没有差异。然而,无论时间如何,高风险双胞胎的双侧背侧前扣带回、下额回和颞顶叶区域的 GM 体积明显大于低风险双胞胎。此外,在随访中出现情感障碍的个体(n=12),与随访时仍保持良好的高风险和低风险双胞胎相比,在右侧背侧前扣带回皮质和右侧下额前皮质的 GM 体积在基线和随访时都相对较大。
这种区域 GM 体积明显稳定增加的模式可能构成具有家族风险的个体发生情感障碍的风险增加的神经标志物。