Multivariate Modeling Strategy for Intercompartmental Analysis of Tissue and Plasma 1H NMR Spectrotypes

被引:36
作者
Montoliu, Ivan [1 ]
Martin, Francois-Pierre J. [1 ]
Collino, Sebastiano [1 ]
Rezzi, Serge [1 ]
Kochhar, Sunil [1 ]
机构
[1] Nestle Res Ctr, BioAnalyt Sci Metabon & Biomarkers, CH-1000 Lausanne 26, Switzerland
关键词
Adrenal gland; Chemometrics; MCR-ALS; MPCA; HRMAS H-1 NMR spectroscopy; Kidney; Liver; Intact tissue; Metabonomics; Pancreas; PARAFAC; PCA; Plasma; METABOLIC INTERACTIONS; SYSTEMS BIOLOGY; SPECTROSCOPY; MODULATION; STRESS; BLOOD;
D O I
10.1021/pr8010205
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multicompartmental metabolic profiling combined with multivariate data analysis offers a unique opportunity to explore the multidimensional metabolic relationships between various biological matrices. Here, we applied unsupervised chemometric methods for integrating H-1 NMR metabolic profiles from mouse plasma, liver, pancreas, adrenal gland and kidney cortex matrices in order to infer intercompartments functional links. Principal Component Analysis (PCA) revealed metabolic differences between matrices but contained limited information on intercompartment metabolic relationships. Multiway PCA enabled the assessment of interindividual metabolic variability across multiple compartments in a single model and, therefore, metabolic correlations between different organs and circulating biofluids. However, this approach does not provide information on the relative contribution of one compartment to another. Integration of metabolic profiles using Multivariate Curve Resolution (MCR) and Parallel Factor Analysis (PARAFAC) methods provided an overview of functional relationships across matrices and enabled the characterization of compartment-specific metabolite signatures, the spectrotypes. In particular, the spectrotypes describe biochemical profiles specific or common to different biological compartments. Consequently, MCR-ALS and PARAFAC appeared to be better adapted for stepwise variable and compartment selection for further correlation analysis. Such a combination of chemometric techniques could provide new research avenues to assess the efficacy of drug or nutritional interventions on targeted organs.
引用
收藏
页码:2397 / 2406
页数:10
相关论文
共 40 条
[1]  
[Anonymous], 1987, J. Chemometrics, DOI DOI 10.1002/CEM.1180010107
[2]   A new efficient method for determining the number of components in PARAFAC models [J].
Bro, R ;
Kiers, HAL .
JOURNAL OF CHEMOMETRICS, 2003, 17 (05) :274-286
[3]   PARAFAC. Tutorial and applications [J].
Bro, R .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 1997, 38 (02) :149-171
[4]   ANALYSIS OF INDIVIDUAL DIFFERENCES IN MULTIDIMENSIONAL SCALING VIA AN N-WAY GENERALIZATION OF ECKART-YOUNG DECOMPOSITION [J].
CARROLL, JD ;
CHANG, JJ .
PSYCHOMETRIKA, 1970, 35 (03) :283-&
[5]  
Craig SAS, 2004, AM J CLIN NUTR, V80, P539
[6]   Adaptation of bacteria to the intestinal niche: Probiotics and gut disorder [J].
Dunne, C .
INFLAMMATORY BOWEL DISEASES, 2001, 7 (02) :136-145
[7]   Metabolic fingerprinting as a diagnostic tool [J].
Ellis, David I. ;
Dunn, Warwick B. ;
Griffin, Julian L. ;
Allwood, J. William ;
Goodacre, Royston .
PHARMACOGENOMICS, 2007, 8 (09) :1243-1266
[8]   Metabolite profiling by one- and two-dimensional NMR analysis of complex mixtures [J].
Fan, WMT .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 1996, 28 (pt 2) :161-219
[9]   High-resolution 1H NMR and magic angle spinning NMR spectroscopic investigation of the biochemical effects of 2-bromoethanamine in intact renal and hepatic tissue [J].
Garrod, S ;
Humpher, E ;
Connor, SC ;
Connelly, JC ;
Spraul, M ;
Nicholson, JK ;
Holmes, E .
MAGNETIC RESONANCE IN MEDICINE, 2001, 45 (05) :781-790
[10]   Integrated metabonomic analysis of the multiorgan effects of hydrazine toxicity in the rat [J].
Garrod, S ;
Bollard, ME ;
Nichollst, AW ;
Connor, SC ;
Connelly, J ;
Nicholson, JK ;
Holmes, E .
CHEMICAL RESEARCH IN TOXICOLOGY, 2005, 18 (02) :115-122