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纤维肌痛症的工作记忆功能障碍与儿茶酚-O-甲基转移酶基因的基因型有关:一项事件相关电位研究。

Working memory dysfunction in fibromyalgia is associated with genotypes of the catechol- O-methyltransferase gene: an event-related potential study.

机构信息

Department of Psychology, School of Health Sciences, Rey Juan Carlos University, Av. Atenas s/n. 28922, Alcorcón, Madrid, Spain.

Emerging Research Group of Anatomical, Molecular and Human Development Bases, Department of Basic Health Sciences, School of Health Sciences, Rey Juan Carlos University, Madrid, Spain.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2023 Feb;273(1):25-40. doi: 10.1007/s00406-022-01488-4. Epub 2022 Sep 13.

Abstract

Recent findings have associated different COMT genotypes with working memory capacity in patients with fibromyalgia. Although it is thought that the COMT gene may influence neural correlates (P2 and P3 ERP components) underlying working memory impairment in this chronic-pain syndrome, it has not yet been explored. Therefore, the aim of the present research was to investigate the potential effect of the COMT gene in fibromyalgia patients on ERP working memory indices (P2 and P3 components). For this purpose, 102 participants (51 patients and 51 healthy control participants) took part in the experiment. Event-related potentials and behavioral responses were recorded while participants performed a spatial n-back task. Participants had to decide if the stimulus coincided or not in the same location as the one presented one (1-back condition) or two (2-back condition) trials before. Genotypes of the COMT gene were determined through a saliva sample from all participants. Present results significantly showed lower working memory performance (p < 0.05) in patients with fibromyalgia as compared to control participants (higher rate of errors and slower reaction times). At neural level, we found that patients exhibited enhanced frontocentral and parieto-occipital P2 amplitudes compared to control participants (p < 0.05). Interestingly, we also observed that only fibromyalgia patients carrying the Val/Val genotype of the COMT gene showed higher frontocentral P2 amplitudes than control participants (p < 0.05). Current results (behavioral outcomes and P2 amplitudes) confirmed the presence of an alteration in working memory functioning in fibromyalgia. The enhancement of frontocentral P2 could be reflecting that these patients would manifest an inefficient way of activating executive attention processes, in carriers of the Val/Val genotype of COMT. To our knowledge, the present findings are the first linking neural indices of working memory dysfunctions and COMT genotypes in fibromyalgia. Applying a subgroup of patient's strategy based on this genetic marker could be useful to establish more tailored therapeutical approaches.

摘要

最近的研究发现,不同的 COMT 基因型与纤维肌痛患者的工作记忆能力有关。虽然人们认为 COMT 基因可能会影响这种慢性疼痛综合征中工作记忆障碍的神经相关性(P2 和 P3 ERP 成分),但尚未对此进行探索。因此,本研究旨在探讨 COMT 基因在纤维肌痛患者中的潜在作用对 ERP 工作记忆指标(P2 和 P3 成分)的影响。为此,102 名参与者(51 名患者和 51 名健康对照组参与者)参加了实验。当参与者执行空间 n 回任务时,记录事件相关电位和行为反应。参与者必须决定刺激是否与前一个(1 回条件)或前两个(2 回条件)试验的相同位置一致。通过所有参与者的唾液样本确定 COMT 基因的基因型。目前的结果显著显示纤维肌痛患者的工作记忆表现较低(p<0.05)与对照组参与者相比(错误率更高,反应时间更慢)。在神经水平上,我们发现与对照组参与者相比,患者表现出增强的额中央和顶枕部 P2 振幅(p<0.05)。有趣的是,我们还观察到只有携带 COMT 基因 Val/Val 基因型的纤维肌痛患者的额中央 P2 振幅高于对照组参与者(p<0.05)。目前的结果(行为结果和 P2 振幅)证实了纤维肌痛患者工作记忆功能的改变。额中央 P2 的增强可能反映了 COMT 基因 Val/Val 基因型携带者在激活执行注意过程中表现出低效的方式。据我们所知,目前的发现是首次将工作记忆功能障碍的神经指数与纤维肌痛中的 COMT 基因型联系起来。基于这种遗传标记,应用患者亚组的策略可能有助于建立更具针对性的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b1/9958168/71fbb399d840/406_2022_1488_Fig1_HTML.jpg

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