Potential of Urinary Metabolites for Diagnosing Multiple Sclerosis

被引:15
作者
Gebregiworgis, Teklab [1 ]
Massilamany, Chandirasegaran [2 ]
Gangaplara, Arunakumar [2 ]
Thulasingam, Sivasubramani [2 ]
Kolli, Venkata [1 ]
Werth, Mark T. [3 ]
Dodds, Eric D. [1 ]
Steffen, David [2 ]
Reddy, Jay [2 ]
Powers, Robert [1 ]
机构
[1] Univ Nebraska Lincoln, Dept Chem, Lincoln, NE 68588 USA
[2] Univ Nebraska Lincoln, Sch Vet Med & Biomed Sci, Lincoln, NE 68588 USA
[3] Nebraska Wesleyan Univ, Dept Chem, Lincoln, NE 68504 USA
基金
美国国家卫生研究院;
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; FINGOLIMOD FTY720; ORAL FINGOLIMOD; T-CELLS; METABOLOMICS; BIOMARKERS; DISCOVERY; RESPONSES; ACIDURIA; BETA;
D O I
10.1021/cb300673e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A definitive diagnostic test for multiple sclerosis (MS) does not exist; instead physicians use a combination of medical history, magnetic resonance imaging, and cerebrospinal fluid analysis (CSF). Significant effort has been employed to identify biomarkers from CSF to facilitate MS diagnosis; however, none of the proposed biomarkers have been successful to date. Urine is a proven source of metabolite biomarkers and has the potential to be a rapid, noninvasive, inexpensive, and efficient diagnostic tool for various human diseases. Nevertheless, urinary metabolites have not been extensively explored as a source of biomarkers for MS. We demonstrate that urinary metabolites have significant promise for monitoring disease-progression, and response to treatment in MS patients. NMR analysis of urine permitted the identification of metabolites that differentiate experimental autoimmune encephalomyelitis (EAE)-mice (prototypic disease model for MS) from healthy and MS drug-treated EAE mice.
引用
收藏
页码:684 / 690
页数:7
相关论文
共 39 条
[21]   Detection of autoreactive CD4 T cells using major histocompatibility complex class II dextramers [J].
Massilamany, Chandirasegaran ;
Upadhyaya, Bijaya ;
Gangaplara, Arunakumar ;
Kuszynski, Charles ;
Reddy, Jay .
BMC IMMUNOLOGY, 2011, 12
[22]   Gender differences in CNS autoimmunity induced by mimicry epitope for PLP 139-151 in SJL mice [J].
Massilamany, Chandirasegaran ;
Thulasingam, Sivasubramani ;
Steffen, David ;
Reddy, Jay .
JOURNAL OF NEUROIMMUNOLOGY, 2011, 230 (1-2) :95-104
[23]   An epitope from Acanthamoeba castellanii that cross-react with proteolipid protein 139-151-reactive T cells induces autoimmune encephalomyelitis in SJL mice [J].
Massilamany, Chandirasegaran ;
Steffen, David ;
Reddy, Jay .
JOURNAL OF NEUROIMMUNOLOGY, 2010, 219 (1-2) :17-24
[24]   A MYELIN OLIGODENDROCYTE GLYCOPROTEIN PEPTIDE INDUCES TYPICAL CHRONIC EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS IN H-2(B) MICE - FINE SPECIFICITY AND T-CELL RECEPTOR V-BETA EXPRESSION OF ENCEPHALITOGENIC T-CELLS [J].
MENDEL, I ;
DEROSBO, NK ;
BENNUN, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (07) :1951-1959
[25]  
Mendel I., 1995, EUR J IMMUNOL, V25, P1951
[26]  
Miller James R, 2004, J Manag Care Pharm, V10, pS4
[27]   SOGGY: Solvent-optimized double gradient spectroscopy for water suppression. A comparison with some existing techniques [J].
Nguyen, Bao D. ;
Meng, Xi ;
Donovan, Kevin J. ;
Shaka, A. J. .
JOURNAL OF MAGNETIC RESONANCE, 2007, 184 (02) :263-274
[28]   FTY720 Ameliorates MOG-Induced Experimental Autoimmune Encephalomyelitis by Suppressing Both Cellular and Humoral Immune Responses [J].
Papadopoulos, Dimitrios ;
Rundle, Jon ;
Patel, Ryan ;
Marshall, Ian ;
Stretton, Jennifer ;
Eaton, Rachel ;
Richardson, Jill C. ;
Gonzalez, Maria I. ;
Philpott, Karen L. ;
Reynolds, Richard .
JOURNAL OF NEUROSCIENCE RESEARCH, 2010, 88 (02) :346-359
[29]   Emerging Disease-Modifying Therapies in Multiple Sclerosis [J].
Perumal, Jai ;
Khan, Omar .
CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2012, 14 (03) :256-263
[30]  
Reeves PG, 1997, J NUTR, V127, pS838