Farshad Goharmanesh, Maryam Masmoie, Hamide Nasiri, Sayedeh-Fatemeh Sadat-Madani, Sara Montazeri Namin, Maryam Damizadeh, Shayan Shakeri, Fatemeh Sodeifian, Ali Rajabpour-Sanati, Bahar Bahrainian, Yasaman Mohammadi, Ali Shushtari, Mahsa Mayeli
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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. 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引用次数: 0
摘要
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和社会经济影响,对全球健康构成了日益严峻的挑战。研究与白质完整性(WMI)相关的代谢改变可以为阿尔茨海默病的发病机制提供重要的见解,并确定潜在的治疗靶点。这项横断面研究探讨了氨基酸(AA)谱(通过超高效液相色谱(UHPLC)评估)与扩散张量成像(DTI)得出的AD个体WMI指标之间的关系。来自阿尔茨海默病神经影像学倡议(ADNI)的176名参与者被纳入研究,并被分为认知正常(CN)个体(n = 54)、轻度认知障碍患者(MCI, n = 88)和AD患者(n = 34)。使用dti衍生的指标评估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)。采用合适的面板进行AA分析。采用回归分析,调整年龄、性别和教育程度,以确定AA水平与WMI之间的显著关联。在各研究组中,明显的AA改变与白质微结构完整性相关。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相关性,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为早期诊断和治疗干预确定新的生物标志物。
Amino acid patterns predict white matter integrity measures in the brain in patients across the Alzheimer's disease continuum.
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.
期刊介绍:
Metabolic Brain Disease serves as a forum for the publication of outstanding basic and clinical papers on all metabolic brain disease, including both human and animal studies. The journal publishes papers on the fundamental pathogenesis of these disorders and on related experimental and clinical techniques and methodologies. Metabolic Brain Disease is directed to physicians, neuroscientists, internists, psychiatrists, neurologists, pathologists, and others involved in the research and treatment of a broad range of metabolic brain disorders.