根据脑容量和认知功能对慢性和发作性偏头痛患者与健康人进行比较

Deniz Kamacı Şener, M. Zarifoğlu, B. Hakyemez, N. Karlı, Nevin Türkeş
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摘要

目标:偏头痛是一种复杂的神经系统疾病:偏头痛是一种复杂的神经系统疾病。除头痛外,偏头痛患者还可能出现脑部结构变化和认知功能障碍。有越来越多的证据表明,偏头痛患者的脑容量和认知功能受损。本研究旨在通过脑磁共振成像、脑容量测量和神经心理学测试,研究偏头痛患者的记忆功能受损情况。研究方法研究对象包括 20 名发作性偏头痛患者、20 名慢性偏头痛患者和 20 名健康对照者。所有参与者的皮层下体积均通过自动分割方法FreeSurfer进行测量。所有研究人员都接受了韦氏记忆量表-修订版(WMS-R)、Stroop测试、瑞文标准进行矩阵、言语流畅性测试和线条定向测试:结果:随着偏头痛持续时间的延长,普坦体积减小;与对照组相比,慢性偏头痛组和发作性偏头痛组的皮层下灰质、左侧小脑皮质和双侧丘脑体积减小;与发作性偏头痛组和对照组相比,慢性偏头痛患者的双侧普坦和右侧小脑皮质体积减小。在神经心理学检查中,延迟记忆会随着偏头痛持续时间的延长而受到影响,慢性偏头痛患者在进行流畅性测试和精神控制测试时会出现障碍。结论是偏头痛患者皮层下体积的变化和认知功能的影响,使人们对偏头痛是否属于良性疾病产生了疑问。结构变化和认知障碍可能是导致偏头痛相关残疾的原因,因此,未来的研究应对这些因果关系进行调查。偏头痛病例中出现的无声梗死、白质损伤和皮质扩散性凹陷可能与皮质下容积变化有关,从而对认知产生影响。在这种情况下,需要对更多样本进行研究,以便更好地了解偏头痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of patients with chronic and episodic migraine with healthy individuals by brain volume and cognitive functions
Objectives: Migraine is a complex neurological disease. In addition to headache, individuals with migraine may develop structural changes inside the brain and cognitive impairment. There is increased evidence associated with impairments in brain volume and cognitive functions in patients with migraine. The present study aimed to investigate the impairment in memory function in individuals with migraine using brain magnetic resonance imaging, volume measurement, and neuropsychological tests. Methods: The study included 20 patients with episodic migraine, 20 patients with chronic migraine, and 20 healthy controls. Subcortical volumes of all participants were measured by FreeSurfer, an automatic segmentation method. The Wechsler Memory Scale-Revised Form (WMS-R), Stroop test, Raven’s Standard Progressive Matrices, Verbal Fluency Test, and Lines Orientation Test were applied in all the study participants. Results: Putamen volume decreased as migraine duration increased, and subcortical gray matter, left cerebellar cortex, and bilateral thalamus volumes were lower in the chronic and episodic group compared to the control group, bilateral putamen and right cerebellar cortex volumes were lower in patients with chronic migraine compared to patients in episodic migraine and control groups. Upon neuropsychological examination, delayed memory was affected as the duration of migraine increased, and there was impairment in patients with chronic migraine upon fluency tests and mental control tests. Conclusions: Changes in subcortical volume and cognitive effects in patients with migraine raise questions about whether migraine qualifies as a benign disease. Structural changes and cognitive impairment may contribute to migraine-associated disability, and therefore, these causalities should be investigated by future studies. Silent infarcts, white matter damage, and cortical spreading depression, which occur in migraine cases, may be associated with subcortical volume changes and thus, cognitive effects. In the context, studies with larger samples to achieve a better understanding are needed.
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