Goharmanesh Farshad, Masmoie Maryam, Nasiri Hamide, Sadat-Madani Sayedeh-Fatemeh, Namin Sara Montazeri, Damizadeh Maryam, Shakeri Shayan, Sodeifian Fatemeh, Rajabpour-Sanati Ali, Bahrainian Bahar, Mohammadi Yasaman, Shushtari Ali, Mayeli Mahsa
Medical Physics and Engineering Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Biomedical Engineering, Shiraz Pasargad Higher Education Institute, Shiraz, Iran.
Metab Brain Dis. 2025 Jun 18;40(6):227. doi: 10.1007/s11011-025-01647-1.
Alzheimer's disease (AD), the leading cause of dementia, poses a growing global health challenge due to its rising prevalence and socioeconomic impact. Investigating metabolic alterations associated with white matter integrity (WMI) could provide critical insights into AD pathogenesis and identify potential therapeutic targets. This cross-sectional study explored the associations between amino acid (AA) profiles, assessed via ultra-high-performance liquid chromatography (UHPLC), and WMI metrics derived from diffusion tensor imaging (DTI) in individuals across the AD continuum. A total of 176 participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) were included and grouped into cognitively normal (CN) individuals (n = 54), patients with mild cognitive impairment (MCI, n = 88), and AD patients (n = 34). WMI was evaluated using DTI-derived metrics, including fractional anisotropy (FA), mean diffusivity (MD), radial diffusivity (RD), and axial diffusivity (AD). AA profiling was conducted using an appropriate panel. Regression analyses, adjusted for age, gender, and education, was used to identify significant associations between AA levels and WMI. Distinct AA alterations were associated with white matter microstructural integrity across study groups. In CN individuals, higher levels of arginine, glycine, and threonine correlated with decreased FA and increased MD, indicating reduced white matter integrity. Conversely, in AD patients, aspartate, glutamate, and histidine exhibited opposite associations, showing positive correlations with FA and negative correlations with MD, suggesting potential neuroprotective or compensatory mechanisms. These findings underscore the associations between AA patterns and white matter integrity and their potential role as AD progression markers. Further investigations into these AA metabolism pathways may identify novel biomarkers for early diagnosis and targets for therapeutic interventions.
阿尔茨海默病(AD)是痴呆症的主要病因,由于其患病率不断上升以及社会经济影响日益增大,对全球健康构成了越来越大的挑战。研究与白质完整性(WMI)相关的代谢改变可为AD发病机制提供关键见解,并确定潜在的治疗靶点。这项横断面研究探讨了通过超高效液相色谱(UHPLC)评估的氨基酸(AA)谱与AD连续体中个体的扩散张量成像(DTI)得出的WMI指标之间的关联。纳入了来自阿尔茨海默病神经影像倡议(ADNI)的176名参与者,并将其分为认知正常(CN)个体(n = 54)、轻度认知障碍(MCI)患者(n = 88)和AD患者(n = 34)。使用DTI得出的指标评估WMI,包括分数各向异性(FA)、平均扩散率(MD)、径向扩散率(RD)和轴向扩散率(AD)。使用适当的检测板进行AA谱分析。采用针对年龄、性别和教育程度进行校正的回归分析来确定AA水平与WMI之间的显著关联。不同的AA改变与各研究组的白质微观结构完整性相关。在CN个体中,较高水平的精氨酸、甘氨酸和苏氨酸与FA降低和MD增加相关,表明白质完整性降低。相反,在AD患者中,天冬氨酸、谷氨酸和组氨酸表现出相反的关联,与FA呈正相关,与MD呈负相关,提示潜在的神经保护或代偿机制。这些发现强调了AA模式与白质完整性之间的关联及其作为AD进展标志物的潜在作用。对这些AA代谢途径的进一步研究可能会确定用于早期诊断的新型生物标志物和治疗干预靶点。