Metabolomic Signature of Diabetic Kidney Disease in Cerebrospinal Fluid and Plasma of Patients with Type 2 Diabetes Using Liquid Chromatography-Mass Spectrometry.
Huan-Tang LinMei-Ling ChengChi-Jen LoGigin LinFu-Chao LiuPublished in: Diagnostics (Basel, Switzerland) (2022)
Diabetic kidney disease (DKD) is the major cause of end stage renal disease in patients with type 2 diabetes mellitus (T2DM). The subtle metabolic changes in plasma and cerebrospinal fluid (CSF) might precede the development of DKD by years. In this longitudinal study, CSF and plasma samples were collected from 28 patients with T2DM and 25 controls, during spinal anesthesia for elective surgery in 2017. These samples were analyzed using liquid chromatography-mass spectrometry (LC-MS) in 2017, and the results were correlated with current DKD in 2017, and the development of new-onset DKD, in 2021. Comparing patients with T2DM having new-onset DKD with those without DKD, revealed significantly increased CSF tryptophan and plasma uric acid levels, whereas phosphatidylcholine 36:4 was lower. The altered metabolites in the current DKD cases were uric acid and paraxanthine in the CSF and uric acid, L-acetylcarnitine, bilirubin, and phosphatidylethanolamine 38:4 in the plasma. These metabolic alterations suggest the defective mitochondrial fatty acid oxidation and purine and phospholipid metabolism in patients with DKD. A correlation analysis found CSF uric acid had an independent positive association with the urine albumin-to-creatinine ratio. In conclusion, these identified CSF and plasma biomarkers of DKD in diabetic patients, might be valuable for monitoring the DKD progression.
Keyphrases
- uric acid
- cerebrospinal fluid
- mass spectrometry
- liquid chromatography
- metabolic syndrome
- fatty acid
- high resolution mass spectrometry
- end stage renal disease
- type diabetes
- peritoneal dialysis
- chronic kidney disease
- high resolution
- nitric oxide
- oxidative stress
- minimally invasive
- adipose tissue
- single cell
- capillary electrophoresis
- coronary artery disease
- skeletal muscle
- acute coronary syndrome
- simultaneous determination
- atrial fibrillation