Weerasekera Akila, Levin Oron, Clauwaert Amanda, Heise Kirstin-Friederike, Hermans Lize, Peeters Ronald, Mantini Dante, Cuypers Koen, Leunissen Inge, Himmelreich Uwe, Swinnen Stephan P
Movement Control & Neuroplasticity Research Group, Department of Movement Sciences, Group Biomedical Sciences, KU Leuven, 3001, Heverlee, Belgium.
Department of Radiology, University Hospitals KU Leuven, 3000, Leuven, Belgium.
Cereb Cortex Commun. 2020 Jun 27;1(1):tgaa028. doi: 10.1093/texcom/tgaa028. eCollection 2020.
Suboptimal inhibitory control is a major factor contributing to motor/cognitive deficits in older age and pathology. Here, we provide novel insights into the neurochemical biomarkers of inhibitory control in healthy young and older adults and highlight putative neurometabolic correlates of deficient inhibitory functions in normal aging. Age-related alterations in levels of glutamate-glutamine complex (Glx), -acetylaspartate (NAA), choline (Cho), and myo-inositol (mIns) were assessed in the right inferior frontal gyrus (RIFG), pre-supplementary motor area (preSMA), bilateral sensorimotor cortex (SM1), bilateral striatum (STR), and occipital cortex (OCC) with proton magnetic resonance spectroscopy (H-MRS). Data were collected from 30 young (age range 18-34 years) and 29 older (age range 60-74 years) adults. Associations between age-related changes in the levels of these metabolites and performance measures or reactive/proactive inhibition were examined for each age group. Glx levels in the right striatum and preSMA were associated with more efficient proactive inhibition in young adults but were not predictive for reactive inhibition performance. Higher NAA/mIns ratios in the preSMA and RIFG and lower mIns levels in the OCC were associated with better deployment of proactive and reactive inhibition in older adults. Overall, these findings suggest that altered regional concentrations of NAA and mIns constitute potential biomarkers of suboptimal inhibitory control in aging.
次优抑制控制是导致老年人运动/认知缺陷及病理状况的主要因素。在此,我们对健康青年和老年成年人抑制控制的神经化学生物标志物提供了新的见解,并强调了正常衰老过程中抑制功能不足的假定神经代谢相关性。利用质子磁共振波谱(H-MRS)对右侧额下回(RIFG)、前辅助运动区(preSMA)、双侧感觉运动皮层(SM1)、双侧纹状体(STR)和枕叶皮层(OCC)中谷氨酸-谷氨酰胺复合物(Glx)、N-乙酰天门冬氨酸(NAA)、胆碱(Cho)和肌醇(mIns)水平的年龄相关变化进行了评估。数据收集自30名青年(年龄范围18 - 34岁)和29名老年(年龄范围60 - 74岁)成年人。针对每个年龄组,研究了这些代谢物水平的年龄相关变化与性能指标或反应性/主动性抑制之间的关联。右侧纹状体和前辅助运动区的Glx水平与青年成年人更有效的主动性抑制相关,但对反应性抑制性能无预测作用。前辅助运动区和右侧额下回中较高的NAA/mIns比值以及枕叶皮层中较低的mIns水平与老年成年人更好地部署主动性和反应性抑制相关。总体而言,这些发现表明,NAA和mIns区域浓度的改变构成了衰老过程中次优抑制控制的潜在生物标志物。