Meyer-Arndt Lil, Hetzer Stefan, Asseyer Susanna, Bellmann-Strobl Judith, Scheel Michael, Stellmann Jan-Patrick, Heesen Christoph, Engel Andreas K, Brandt Alexander U, Haynes John-Dylan, Paul Friedemann, Gold Stefan M, Weygandt Martin
Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, And Berlin Institute of Health, NeuroCure Clinical Research Center, 10117, Berlin, Germany.
Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, And Berlin Institute of Health, Berlin Center for Advanced Neuroimaging, 10117, Berlin, Germany.
Neurobiol Stress. 2020 Jul 27;13:100244. doi: 10.1016/j.ynstr.2020.100244. eCollection 2020 Nov.
Multiple sclerosis (MS) is characterized by two neuropathological key aspects: inflammation and neurodegeneration. Clinical studies support a prospective link between psychological stress and subsequent inflammatory disease activity. However, it is unknown if a similar link exists for grey matter (GM) degeneration as the key driver of irreversible disability.
We tested whether neural network activity triggered in a psychological fMRI stress paradigm (a mental arithmetic task including social evaluation) conducted at a baseline time point predicts future GM atrophy in 25 persons with MS (14 females). Atrophy was determined between the baseline and a follow-up time point with a median delay of 1012 (Rg: 717-1439) days. Additionally, atrophy was assessed in 22 healthy subjects (13 females; median delay 771 [Rg: 740-908] days between baseline and follow-up) for comparison.
An analysis of longitudinal atrophy in patients revealed GM loss in frontal, parietal, and cerebellar areas. Cerebellar atrophy was more pronounced in patients than controls. Future parietal and cerebellar atrophy could be predicted based on activity of two networks. Perceived psychological stress was negatively related to future parietal atrophy in patients and activity of the network predictive of parietal atrophy was positively linked to perceived stress.
We have shown that blunted neural and psychological stress processing have a detrimental effect on the course of MS and are interrelated. Together with research showing that psychological and neural stress processing can be altered through interventions, our findings suggest that stress processing might constitute an important modifiable disease factor.
多发性硬化症(MS)具有两个神经病理学关键特征:炎症和神经退行性变。临床研究支持心理应激与随后的炎症性疾病活动之间存在前瞻性联系。然而,作为不可逆残疾的关键驱动因素,灰质(GM)退化是否存在类似联系尚不清楚。
我们测试了在基线时间点进行的心理功能磁共振成像应激范式(包括社会评价的心理算术任务)中触发的神经网络活动是否能预测25例MS患者(14名女性)未来的GM萎缩。在基线和随访时间点之间确定萎缩情况,中位延迟为1012(范围:717 - 1439)天。此外,对22名健康受试者(13名女性;基线和随访之间的中位延迟为771 [范围:740 - 908]天)进行萎缩评估以作比较。
对患者纵向萎缩的分析显示额叶、顶叶和小脑区域存在GM丢失。患者的小脑萎缩比对照组更明显。未来的顶叶和小脑萎缩可以根据两个网络的活动来预测。患者感知到的心理应激与未来的顶叶萎缩呈负相关,预测顶叶萎缩的网络活动与感知到的应激呈正相关。
我们已经表明,神经和心理应激处理迟钝对MS病程有不利影响且相互关联。连同表明心理和神经应激处理可以通过干预改变的研究,我们的发现表明应激处理可能是一个重要的可改变的疾病因素。