Liu Xiaoguang, Baxley Sean, Hebron Michaeline, Turner Raymond Scott, Moussa Charbel
Laboratory for Dementia and Parkinsonism, Translational Neurotherapeutics Program, Department of Neurology, Georgetown University Medical Center, Washington, DC 20057, USA.
Interdisciplinary Program in Neuroscience, Georgetown University Medical Center, Washington, DC 20057, USA.
Int J Mol Sci. 2025 May 23;26(11):5044. doi: 10.3390/ijms26115044.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder that is characterized by amyloid-beta (Aβ) accumulation and neuroinflammation. A previous multicenter, phase 2, double-blind, placebo-controlled trial randomized 179 participants into placebo or resveratrol over 52 weeks. Sub-analysis of CSF biomarkers of neuronal damage, inflammation, and microglial activity was performed in a subset of patients treated with a placebo (n = 21) versus resveratrol (n = 30). Markers of neuronal damage, including neuron-specific enolase and hyperphosphorylated neurofilaments, were reduced. Microglial activation was measured via a triggering receptor expressed on myeloid cells (TREM)-2 at baseline and after resveratrol treatment. Resveratrol significantly reduced CSF TREM2 levels and decreased inflammation and tissue damage, including matrix metalloprotease (MMP)-9. Cathepsin D, a lysosomal marker of autophagy, was reduced in the resveratrol group compared with placebo, while angiogenin, a marker of vascular angiogenesis, was increased. These data suggest that resveratrol may exert anti-inflammatory and neuroprotective effects in AD by reducing CSF TREM2 and other markers of neuronal damage. Further research is needed to assess the significance of these biomarker changes on clinical outcomes in patients with neurodegenerative diseases.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征为β-淀粉样蛋白(Aβ)积累和神经炎症。先前一项多中心、2期、双盲、安慰剂对照试验将179名参与者在52周内随机分为安慰剂组或白藜芦醇组。对接受安慰剂治疗(n = 21)与白藜芦醇治疗(n = 30)的部分患者进行了脑脊液中神经元损伤、炎症和小胶质细胞活性生物标志物的亚组分析。包括神经元特异性烯醇化酶和过度磷酸化神经丝在内的神经元损伤标志物减少。在基线和白藜芦醇治疗后,通过髓样细胞表达的触发受体(TREM)-2测量小胶质细胞活化。白藜芦醇显著降低脑脊液TREM2水平,并减少炎症和组织损伤,包括基质金属蛋白酶(MMP)-9。与安慰剂组相比,白藜芦醇组中自噬的溶酶体标志物组织蛋白酶D减少,而血管生成标志物血管生成素增加。这些数据表明,白藜芦醇可能通过降低脑脊液TREM2和其他神经元损伤标志物在AD中发挥抗炎和神经保护作用。需要进一步研究来评估这些生物标志物变化对神经退行性疾病患者临床结局的意义。