Quantitative metabolomic profiling of serum, plasma, and urine by (1)H NMR spectroscopy discriminates between patients with inflammatory bowel disease and healthy individuals.
Quantitative metabolomic profiling of serum, plasma, and urine by (1)H NMR spectroscopy discriminates between patients with inflammatory bowel disease and healthy individuals.
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DOI:
10.1021/pr300139q
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发表时间:
2012-06-01
影响因子:
4.4
通讯作者:
Storr M
中科院分区:
文献类型:
--
作者:
Schicho R;Shaykhutdinov R;Ngo J;Nazyrova A;Schneider C;Panaccione R;Kaplan GG;Vogel HJ;Storr M
Serologic biomarkers for inflammatory bowel disease (IBD) have yielded variable differentiating ability. Quantitative analysis of a large number of metabolites is a promising method to detect IBD biomarkers. Human subjects with active Crohn’s disease (CD) and active ulcerative colitis (UC) were identified, and serum, plasma, and urine specimens were obtained. We characterized 44 serum, 37 plasma, and 71 urine metabolites by use of 1H NMR spectroscopy and “targeted analysis” to differentiate between diseased and non-diseased individuals, as well as between the CD and UC cohorts. We used multiblock principal component analysis and hierarchical OPLS-DA for comparing several blocks derived from the same “objects” (e.g., subject) to examine differences in metabolites. In serum and plasma of IBD patients, methanol, mannose, formate, 3-methyl-2-oxovalerate, and amino acids such as isoleucine were the metabolites most prominently increased, whereas in urine, maximal increases were observed for mannitol, allantoin, xylose, and carnitine. Both serum and plasma of UC and CD patients showed significant decreases in urea and citrate, whereas in urine, decreases were observed, among others, for betaine and hippurate. Quantitative metabolomic profiling of serum, plasma, and urine discriminates between healthy and IBD subjects. However, our results show that the metabolic differences between the CD and UC cohorts are less pronounced.
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影响因子:
56.9
作者:
ERIKSEN, SP
通讯作者:
ERIKSEN, SP
DOI:
10.1016/s0731-7085(03)00410-2
发表时间:
2003-12-04
影响因子:
3.4
作者:
Lenz, EM;Bright, J;Nash, AFP
通讯作者:
Nash, AFP
影响因子:
2.9
作者:
Liu, Linsheng;Aa, Jiye;Wu, Zimei
通讯作者:
Wu, Zimei
影响因子:
4.9
作者:
Hanauer, SB
通讯作者:
Hanauer, SB
影响因子:
2.5
作者:
Balasubramanian, Krithika;Kumar, Sandeep;Jagannathan, Naranamangalam R.
通讯作者:
Jagannathan, Naranamangalam R.