Metabolomic analysis and signatures in motor neuron disease

被引:127
作者
Rozen, Steve [1 ,2 ]
Cudkowicz, Merit E. [3 ]
Bogdanov, Mikhail [4 ]
Matson, Wayne R. [5 ]
Kristal, Bruce S. [4 ,6 ]
Beecher, Chris [1 ]
Harrison, Scott [1 ]
Vouros, Paul [7 ]
Flarakos, Jimmy [7 ]
Vigneau-Callahan, Karen [5 ]
Matson, Theodore D. [8 ]
Newhall, Kristyn M. [3 ]
Beal, M. Flint [4 ]
Brown, Robert H., Jr. [9 ]
Kaddurah-Daouk, Rima [1 ]
机构
[1] Metabolon Inc, Res Triangle Pk, NC 27709 USA
[2] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[3] Massachusetts Gen Hosp, Neurol Clin Trial Unit, Charlestown, MA 02129 USA
[4] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[5] ESA Inc, Chelmsford, MA 01824 USA
[6] Burke Med Res Inst, Dementia Res Serv, White Plains, NY 10605 USA
[7] Northeastern Univ, Dept Chem, Boston, MA 02115 USA
[8] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[9] Massachusetts Gen Hosp E, MGH, Charlestown, MA 02129 USA
基金
美国国家卫生研究院;
关键词
amyotrophic lateral sclerosis; motor neuron disease; coulometric array; metabolic profiling;
D O I
10.1007/s11306-005-4810-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Motor neuron diseases (MND) are a heterogeneous group of disorders that includes amyotrophic lateral sclerosis (ALS) and result in death of motor neurons. These diseases may produce characteristic perturbations of the metabolome, the collection of small-molecules (metabolites) present in a cell, tissue, or organism. To test this hypothesis, we used high performance liquid chromatography followed by electrochemical detection to profile blood plasma from 28 patients with MND and 30 healthy controls. Of 317 metabolites, 50 were elevated in MND patients and more than 70 were decreased (p < 0.05). Among the compounds elevated, 12 were associated with the drug Riluzole. In a subsequent study of 19 subjects with MND who were not taking Riluzole and 33 healthy control subjects, six compounds were significantly elevated in MND, while the number of compounds with decreased concentration was similar to study 1. Our data also revealed a distinctive signature of highly correlated metabolites in a set of four patients, three of whom had lower motor neuron (LMN) disease. In both datasets we were able to separate MND patients from controls using multivariate regression techniques. These results suggest that metabolomic studies can be used to ascertain metabolic signatures of disease in a non-invasive fashion. Elucidation of the structures of signature molecules in ALS and other forms of MND should provide insight into aberrant biochemical pathways and may provide diagnostic markers and targets for drug design.
引用
收藏
页码:101 / 108
页数:8
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