TY - JOUR
T1 - The dynamic range of the human metabolome revealed by challenges
AU - Krug, Susanne
AU - Kastenmüller, Gabi
AU - Stückler, Ferdinand
AU - Rist, Manuela J.
AU - Skurk, Thomas
AU - Sailer, Manuela
AU - Raffler, Johannes
AU - Römisch-Margl, Werner
AU - Adamski, Jerzy
AU - Prehn, Cornelia
AU - Frank, Thomas
AU - Engel, Karl Heinz
AU - Hofmann, Thomas
AU - Luy, Burkhard
AU - Zimmermann, Ralf
AU - Moritz, Franco
AU - Schmitt-Kopplin, Philippe
AU - Krumsiek, Jan
AU - Kremer, Werner
AU - Huber, Fritz
AU - Oeh, Uwe
AU - Theis, Fabian J.
AU - Szymczak, Wilfried
AU - Hauner, Hans
AU - Suhre, Karsten
AU - Daniel, Hannelore
PY - 2012/6
Y1 - 2012/6
N2 - Metabolic challenge protocols, such as the oral glucose tolerance test, can uncover early alterations in metabolism preceding chronic diseases. Nevertheless, most metabolomics data accessible today reflect the fasting state. To analyze the dynamics of the human metabolome in response to environmental stimuli, we submitted 15 young healthy male volunteers to a highly controlled 4 d challenge protocol, including 36 h fasting, oral glucose and lipid tests, liquid test meals, physical exercise, and cold stress. Blood, urine, exhaled air, and breath condensate samples were analyzed on up to 56 time points by MS- and NMR-based methods, yielding 275 metabolic traits with a focus on lipids and amino acids. Here, we show that physiological challenges increased interindividual variation even in phenotypically similar volunteers, revealing metabotypes not observable in baseline metabolite profiles; volunteer-specific metabolite concentrations were consistently reflected in various biofluids; and readouts from a systematic model of β-oxidation (e.g., acetylcarnitine/ palmitylcarnitine ratio) showed significant and stronger associations with physiological parameters (e.g., fat mass) than absolute metabolite concentrations, indicating that systematic models may aid in understanding individual challenge responses. Due to the multitude of analytical methods, challenges and sample types, our freely available metabolomics data set provides a unique reference for future metabolomics studies and for verification of systems biology models.
AB - Metabolic challenge protocols, such as the oral glucose tolerance test, can uncover early alterations in metabolism preceding chronic diseases. Nevertheless, most metabolomics data accessible today reflect the fasting state. To analyze the dynamics of the human metabolome in response to environmental stimuli, we submitted 15 young healthy male volunteers to a highly controlled 4 d challenge protocol, including 36 h fasting, oral glucose and lipid tests, liquid test meals, physical exercise, and cold stress. Blood, urine, exhaled air, and breath condensate samples were analyzed on up to 56 time points by MS- and NMR-based methods, yielding 275 metabolic traits with a focus on lipids and amino acids. Here, we show that physiological challenges increased interindividual variation even in phenotypically similar volunteers, revealing metabotypes not observable in baseline metabolite profiles; volunteer-specific metabolite concentrations were consistently reflected in various biofluids; and readouts from a systematic model of β-oxidation (e.g., acetylcarnitine/ palmitylcarnitine ratio) showed significant and stronger associations with physiological parameters (e.g., fat mass) than absolute metabolite concentrations, indicating that systematic models may aid in understanding individual challenge responses. Due to the multitude of analytical methods, challenges and sample types, our freely available metabolomics data set provides a unique reference for future metabolomics studies and for verification of systems biology models.
KW - Clinical study
KW - Human physiology
KW - Nutrition
KW - Systems biology
KW - Time-resolved fingerprinting
UR - http://www.scopus.com/inward/record.url?scp=84861790964&partnerID=8YFLogxK
U2 - 10.1096/fj.11-198093
DO - 10.1096/fj.11-198093
M3 - Article
C2 - 22426117
AN - SCOPUS:84861790964
SN - 0892-6638
VL - 26
SP - 2607
EP - 2619
JO - FASEB Journal
JF - FASEB Journal
IS - 6
ER -