Quantitative metabolomics of saliva using proton NMR spectroscopy in patients with Parkinson's disease and healthy controls

被引:56
|
作者
Kumari, Sadhana [1 ,2 ]
Goyal, Vinay [3 ]
Kumaran, S. Senthil [1 ,2 ]
Dwivedi, S. N. [4 ]
Srivastava, Achal [3 ]
Jagannathan, N. R. [1 ,2 ]
机构
[1] All India Inst Med Sci, Dept NMR, New Delhi 110029, India
[2] All India Inst Med Sci, MRI Facil, New Delhi 110029, India
[3] All India Inst Med Sci, Dept Neurol, New Delhi 110029, India
[4] All India Inst Med Sci, Dept Biostat, New Delhi 110029, India
关键词
Parkinson's disease; Salivary metabolomics; NMR; Biomarkers; Malabsorption; Spectroscopy; CHAIN FATTY-ACIDS; ALPHA-SYNUCLEIN; GUT MICROBIOTA; BIOMARKERS; METABOLISM; INTESTINE; DIAGNOSIS; PLASMA;
D O I
10.1007/s10072-019-04143-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Parkinson's disease (PD) is a multisystem disorder of unknown etiology, highlights a broad array of symptoms and pathological features influencing organs throughout the body. The metabolic profile of saliva in patients with PD may be influenced by malabsorption in the gastroenteric tract, neurodegeneration, and mitochondrial dysfunction. In the present study, we apply a powerful NMR metabolomics approach for biomarker identification in PD using saliva, a non-invasive bio-fluid. Methods Metabolic profiling of saliva were studied in patients with PD (n = 76) and healthy controls (HC, n = 37) were analyzed and differentiated PD from HC. A total of 40 metabolites including aromatic amino acids, short-chain fatty acids, branched chain amino acids, taurine, and N-acetylglutamate were identified. Spectral binned data and concentration of metabolites were estimated for analysis. Results Increased concentration of phenylalanine, tyrosine, histidine, glycine, acetoacetate, taurine, TMAO, GABA, N-acetylglutamate, acetoin, acetate, alanine, fucose, propionate, isoleucine, and valine were observed in PD as compared to HC. Further, subgroup analysis among early PD, advanced PD, and HC groups, revealed increased metabolite concentration in early PD group as compared to advanced PD and HC group. Discussion Analysis revealed potential biomarkers and their involvement in amino acid metabolism, energy metabolism, neurotransmitters metabolism, and microflora system. Patients with early PD exhibited higher metabolite concentration as compared to advanced PD group which might be associated with dopaminergic treatment. Conclusion The results of our data indicate that patients with PD might be characterized by metabolic imbalances like gut microflora system, energy metabolites, and neurotransmitters which may contribute to the PD pathogenesis.
引用
收藏
页码:1201 / 1210
页数:10
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