Serum indoxyl sulfate predicts adverse cardiovascular events in patients with chronic kidney disease

Pei-Chun Fan1, Jason Chih-Hsiang Chang1, Chia-Ni Lin2

  • 1Kidney Research Center, Department of Nephrology, Chang Gung Memorial Hospital, Linkou Medical Center, Taiwan; Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

Insights

Serum indoxyl sulfate (IS) levels can predict major adverse cardiovascular events (MACEs) in patients with chronic kidney disease (CKD). This finding highlights IS as a potential biomarker for cardiovascular risk in CKD patients.

Area of Science:

  • Nephrology
  • Cardiology
  • Biomarker Discovery

Background:

  • Indoxyl sulfate (IS) is a protein-bound uremic toxin known to cause cardiovascular (CV) toxicity.
  • Chronic kidney disease (CKD) patients exhibit elevated IS levels.
  • The predictive value of IS for CV events in CKD is not fully established.

Purpose of the Study:

  • To investigate the association between serum IS levels and the risk of major adverse cardiovascular events (MACEs) in patients with CKD.
  • To determine if IS can serve as a predictive biomarker for CV outcomes in this population.

Main Methods:

  • A cohort of 147 patients with CKD stages 1-5 was followed for 3 years.
  • Serum IS levels were quantified using mass spectrometry.
  • Multivariable Cox regression analysis was employed to assess the predictive value of IS for MACEs, controlling for demographics.

Main Results:

  • A significant proportion of patients (32.0%) experienced MACEs during the follow-up period.
  • Elevated serum IS levels were independently associated with an increased risk of MACEs.
  • The area under the receiver operating characteristic curve (AUC) for IS was 0.708, indicating moderate predictive accuracy.

Conclusions:

  • Serum IS levels demonstrate potential as a predictive biomarker for cardiovascular disease in patients with CKD.
  • These findings suggest a critical role for IS in CV risk stratification for CKD patients.
  • Larger-scale studies are recommended to further validate these results.
Abstract

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