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首页> 外文期刊>The journal of headache and pain >EHMTI-0393. Abnormal ictal large-scale network connectivity in migraine without aura: a resting-state functional connectivity study
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EHMTI-0393. Abnormal ictal large-scale network connectivity in migraine without aura: a resting-state functional connectivity study

机译:EHMTI-0393。没有先兆的偏头痛中异常的大范围大规模网络连接:静止状态功能连接研究

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Alterations in cerebral resting-state functional connectivity (RSFC) have been reported outside of migraine attacks. To date, no studies studied possible changes in RSFC during migraine attacks. To investigate resting-state functional connectivity in salience (SN), sensorimotor (SMN) and default mode networks (DMN) during the early phase of pituitary adenylate cyclase-activating polypeptide-38 (PACAP38)-induced migraine attacks. In a double-blind randomized study, 24 female migraine patients without aura received intravenous PACAP38 or vasoactive intestinal polypeptide (VIP) for 20 min. Both peptides are closely related and cause vasodilatation, but only PACAP38 induces migraine attacks. VIP was therefore used as an active placebo. Functional MRI was recorded before and during PACAP38-induced attacks (n=16) and before and after VIP infusion (n=15). Data were analyzed by SPM8 and the REST toolbox for Matlab in a seed-based fashion. During PACAP38-induced attacks, we found increased connectivity of the bilateral opercular part of the inferior frontal gyrus (Brodmann area 44) in the SN. In SMN, there was increased connectivity in the right premotor cortex and decreased activity in the left visual cortex. Several areas showed increased (left primary auditory, secondary somatosensory, premotor and visual cortices, and left superior longitudinal fascicle) and decreased (right cerebellum and left frontal lobe) connectivity in DMN. We found no resting-state network changes after VIP. The early phases of PACAP38-induced migraine attacks are associated with altered connectivity of several large-scale functional networks of the brain.
机译:据报道,偏头痛发作后大脑静止状态功能连接性(RSFC)发生改变。迄今为止,尚无研究研究偏头痛发作期间RSFC的可能变化。在垂体腺苷酸环化酶激活多肽-38(PACAP38)诱发的偏头痛发作早期,研究显着性(SN),感觉运动(SMN)和默认模式网络(DMN)中的静止状态功能连接。在一项双盲随机研究中,24名没有先兆的女性偏头痛患者接受了静脉注射PACAP38或血管活性肠多肽(VIP)20分钟。两种肽都密切相关并引起血管舒张,但只有PACAP38诱导偏头痛发作。因此,VIP被用作积极的安慰剂。在PACAP38引起的发作之前和期间(n = 16)以及VIP输注之前和之后(n = 15)记录了功能性MRI。 SPM8和用于Matlab的REST工具箱以基于种子的方式分析了数据。在PACAP38诱导的攻击中,我们发现了SN中下额回的双侧可操作部分(Brodmann区域44)的连通性增加。在SMN中,右前运动皮层的连接性增加,而左视皮层的活动性降低。在DMN中,有几个区域显示增加(左原发听觉,继发的躯体感觉,运动前和视觉皮层以及左上纵束)和下降(右小脑和左额叶)的连通性。 VIP后,我们发现静止状态网络没有变化。 PACAP38诱发的偏头痛发作的早期阶段与大脑几个大型功能网络的连通性改变有关。

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