Methods and potential biomarkers for the evaluation of endothelial dysfunction in chronic kidney disease: a critical

Simona M Hogas1, Luminita Voroneanu, Dragomir N Serban

  • 1Nephrology Clinic at C. I. Parhon University Hospital, Gr. T. Popa University of Medicine and Pharmacy, Iasi, Romania.

Insights

Chronic kidney disease (CKD) patients face high cardiovascular risks due to endothelial dysfunction (ED). Early diagnosis using combined biomarker and bedside methods is crucial for better treatment strategies.

Area of Science:

  • Nephrology
  • Cardiovascular Medicine
  • Vascular Biology

Background:

  • Chronic kidney disease (CKD) is linked to significant cardiovascular morbidity and mortality.
  • Endothelial dysfunction (ED), arterial stiffness, and vascular calcifications are key contributors to cardiovascular events in CKD.
  • Vascular abnormalities in CKD patients are often more severe than in other high-risk groups and typically go undiagnosed.

Purpose of the Study:

  • To review the causes and risk factors of ED, oxidative stress, and inflammation in CKD.
  • To describe methods for investigating ED and the role of biomarkers.
  • To discuss the diagnostic and therapeutic implications of novel ED markers in CKD.

Main Methods:

  • Review of literature on causes, risk factors, and investigation of ED in CKD.
  • Description of methods including plethysmography, laser Doppler, Doppler ultrasound, and applanation tonometry.
  • Discussion of biomarkers and clinical assessment tools for ED and arterial stiffness.

Main Results:

  • ED, arterial stiffness, and vascular calcifications are major drivers of cardiovascular complications in CKD.
  • Standard clinical settings often miss the diagnosis of abnormal vascular reactivity in CKD.
  • Applanation tonometry offers a reliable bedside assessment of arterial stiffness and vascular reactivity.

Conclusions:

  • A comprehensive assessment combining biomarkers and bedside investigational approaches is needed for ED in CKD.
  • Improving endothelial function remains a significant clinical challenge with limited therapeutic options.
  • Developing optimal therapeutic tools requires a multi-faceted diagnostic strategy.

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