Author/Authors :
Hayashi, Kaori Department of Internal Medicine - School of Medicine - Keio University - Tokyo, Japan , Sasamura, Hiroyuki Department of Internal Medicine - School of Medicine - Keio University - Tokyo, Japan , Hishiki, Takako Department of Biochemistry - School of Medicine - Keio University - Tokyo, Japan , Suematsu, Makoto Department of Biochemistry - School of Medicine - Keio University - Tokyo, Japan , Ikeda, Satsuki Institute for Advanced Biosciences - Keio University - Yamagata, Japan , Soga, Tomoyoshi Institute for Advanced Biosciences - Keio University - Yamagata, Japan , Itoh, Hiroshi Department of Internal Medicine - School of Medicine - Keio University - Tokyo, Japan
Abstract :
Background: Chronic kidney disease (CKD) is a major health problem throughout the
world, and understanding the pathological condition of CKD has become increasingly
important. The recent development of advanced metabolomic assay techniques
now allows the human metabolic condition to be evaluated sensitively and comprehensively.
Objectives: The aim of this study was to use metabolomic analysis to perform a preliminary
survey of metabolic changes occurring in patients with stage 1-2 CKD.
Patients and Methods: Serum and urine metabolomic profiles of 15 patients with stage
1-2 CKD were analyzed using our previously reported capillary electrophoresis time-offlight
mass spectrometry (CE-TOFMS) systems, and compared to 7 healthy volunteers.
Results: The CE-TOFMS systems in three different modes for cation, anion, and nucleotide
analyses detected multiple metabolites in serum and urine samples. In cation
analysis mode, several increases in nonessential amino acids were identified in patients
with stage 1-2 CKD, similar to those reported for end-stage renal disease (ESRD).
Free-radical scavengers carnosine and hypotaurine were decreased in the urine,
whereas serum hypotaurine and taurine were increased, consistent with changes in
renal and/or systemic oxidative stress. Moreover, the cardiotoxin hypoxanthine was
markedly increased in the serum, whereas serum and urine adenosine and urine guanine
were decreased, suggesting changes in purine nucleotide metabolism which
could affect cardiovascular prognosis. Changes in other unidentified metabolites
were also detected.
Conclusions: These results suggest that multiple changes in the metabolism are already
detectable in stage 1-2 CKD using metabolome analysis. Further studies on these
metabolic changes may result in new strategies to prevent cardiovascular events and
progression to ESRD in patients with CKD.