Plasma amino acids patterns and age of onset of amyotrophic lateral sclerosis

被引:6
作者
Cecchi, Matteo [1 ]
Messina, Paolo [2 ]
Airoldi, Luisa [1 ]
Pupillo, Elisabetta [2 ]
Di Poggio, Monica Bandettini [3 ]
Calvo, Andrea [4 ]
Filosto, Massimiliano [5 ]
Lunetta, Christian [6 ]
Mandrioli, Jessica [7 ]
Pisa, Federica [8 ]
Pastorelli, Roberta [1 ]
Beghi, Ettore [2 ]
机构
[1] IRCCS, Ist Ric Farmacol Mario Negri, Mol Toxicol Lab, Milan, Italy
[2] IRCCS, Ist Ric Farmacol Mario Negri, Lab Neurol Disorders, Milan, Italy
[3] Univ Genoa, Dept Neurosci, Genoa, Italy
[4] Univ Turin, Dept Neurol, I-10124 Turin, Italy
[5] Univ Hosp Spedali Civili, Sect Neuromuscular Dis & Neuropathies, Brescia, Italy
[6] Osped Niguarda Ca Granda, Fdn Serena Onlus, Ctr Clin NEMO, Milan, Italy
[7] Univ Modena & Reggio Emilia, SantAgostino Estense Hosp, Dept Neurosci, Modena, Italy
[8] Univ Hosp Udine, Inst Hyg & Clin Epidemiol, Udine, Italy
关键词
Amyotrophic lateral sclerosis; plasma amino acids; age at onset; spectrometry; GLUTAMATE; ALS;
D O I
10.3109/21678421.2014.920032
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
The aim of this study was to verify whether abnormalities in plasma amino acid (AA) levels could be biological correlates of the age of onset in amyotrophic lateral sclerosis (ALS). We undertook plasma AA profiling in a large population comprising 117 newly diagnosed ALS patients and 117 matched controls. ALS patients were stratified in early (58 patients aged < 55 years) versus late onset (59 patients aged > 74 years). We applied a rapid and reproducible method for the analysis of AA using amine reactive isotope coded tags in conjunction with liquid chromatography coupled to Multiple Reaction Monitoring-Mass Spectrometry. Results showed that values of only three AA were significantly different in ALS patients and controls. We found lower levels of leucine and higher levels of glutamate and leucine in early-onset ALS compared to their matched controls. In conclusion, different AA patterns related to the ALS age of onset were found, providing insight into possibly aberrant biochemical pathways that might unlock key pathological pathways.
引用
收藏
页码:371 / 375
页数:5
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