Jensen Camilla Steen, Portelius Erik, Høgh Peter, Wermuth Lene, Blennow Kaj, Zetterberg Henrik, Hasselbalch Steen Gregers, Simonsen Anja Hviid
Danish Dementia Research Centre, Department of Neurology, Rigshospitalet University of Copenhagen, Copenhagen, Denmark.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Alzheimers Dement (N Y). 2017 Apr 17;3(2):284-290. doi: 10.1016/j.trci.2017.03.007. eCollection 2017 Jun.
Physical exercise has gained increasing focus as a potential mean to maintain cognitive function in patients with Alzheimer's disease (AD). Alongside the markers of specific AD pathology (amyloid β and tau), other pathologies such as neuronal damage and synaptic loss have been proposed as markers of the disease. Here, we study the effect of physical exercise on biomarkers of neuronal and synaptic integrity.
Cerebrospinal fluid (CSF) from 51 AD subjects who participated in the randomized controlled trial Preserving Cognition, Quality of Life, Physical Health and Functional Ability in Alzheimer's Disease: The Effect of Physical Exercise (ADEX) was analyzed for the concentration of neurofilament light (NFL), neurogranin (Ng), visinin-like protein-1 (VILIP-1), and chitinase-3-like protein 1 (YKL-40). Participants were subjected to either 16 weeks of moderate- to high-intensity exercise ( = 25) or treatment as usual (control group, = 26), and CSF was collected before and after intervention.
No significant differences in CSF concentrations of VILIP-1, YKL-40, NFL, and Ng were observed when comparing mean change from baseline between the exercise and control groups. Similarly, when classifying subjects based on their exercise levels, no significant changes were observed for the biomarkers in the control group compared with the high-exercise group (attending 80% of the exercise sessions with an intensity of 70% of maximum heart rate or above).
These results are not supportive of a modulatory effect of physical exercise on the selected biomarkers of neuronal and synaptic integrity in patients with AD.
体育锻炼作为维持阿尔茨海默病(AD)患者认知功能的一种潜在手段,已受到越来越多的关注。除了特定AD病理学标志物(淀粉样β蛋白和tau蛋白)外,其他病理学特征如神经元损伤和突触丧失也被认为是该疾病的标志物。在此,我们研究体育锻炼对神经元和突触完整性生物标志物的影响。
对51名参与随机对照试验“阿尔茨海默病中维持认知、生活质量、身体健康和功能能力:体育锻炼的影响(ADEX)”的AD患者的脑脊液(CSF)进行分析,检测神经丝轻链(NFL)、神经颗粒蛋白(Ng)、类视黄醛蛋白-1(VILIP-1)和几丁质酶-3样蛋白1(YKL-40)的浓度。参与者被随机分为两组,一组进行16周的中度至高强度运动(n = 25),另一组接受常规治疗(对照组,n = 26),并在干预前后收集脑脊液。
比较运动组和对照组从基线开始的平均变化时,未观察到VILIP-1、YKL-40、NFL和Ng的脑脊液浓度有显著差异。同样,根据运动水平对受试者进行分类时,与高运动组(参加80%的运动课程,强度为最大心率的70%或以上)相比,对照组的生物标志物没有显著变化。
这些结果不支持体育锻炼对AD患者所选神经元和突触完整性生物标志物具有调节作用。