Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease

Anthony Dosseto1, Kelly Lambert2, Hicham I Cheikh Hassan2,3

  • 1Wollongong Isotope Geochronology Laboratory, School of Earth, Atmospheric and Life Sciences, University of Wollongong, Wollongong, New South Wales, Australia.

Insights

New research suggests serum calcium isotope ratios (δ44/42Ca) can noninvasively detect vascular calcification in chronic kidney disease (CKD) patients, outperforming current biomarkers.

Area of Science:

  • Nephrology
  • Biochemistry
  • Cardiovascular Medicine

Background:

  • Abnormal calcium balance in chronic kidney disease (CKD) contributes to vascular calcification.
  • Screening for vascular calcification is not standard practice in CKD patients.
  • Existing biomarkers for vascular calcification lack optimal diagnostic utility.

Purpose of the Study:

  • To investigate serum calcium (Ca) isotope ratios (44Ca/42Ca) as a noninvasive marker for vascular calcification in CKD.
  • To compare the diagnostic performance of serum δ44/42Ca with existing biomarkers.

Main Methods:

  • Cross-sectional study involving 78 participants (controls, mild-moderate CKD, dialysis, kidney transplant).
  • Measured serum and urine calcium concentrations and isotope ratios (δ44/42Ca).
  • Assessed clinical parameters including blood pressure, ankle brachial index, pulse wave velocity, and estimated glomerular filtration rate.

Main Results:

  • Serum δ44/42Ca values significantly differed between healthy controls, mild-moderate CKD, and dialysis groups (P < 0.01).
  • Urine δ44/42Ca showed no significant differences across groups.
  • Serum δ44/42Ca demonstrated very good diagnostic utility for medial artery calcification (AUC = 0.818, sensitivity 81.8%, specificity 77.3%, P < 0.01).

Conclusions:

  • Serum δ44/42Ca shows potential as an early, noninvasive screening tool for vascular calcification in CKD.
  • This novel biomarker may offer superior diagnostic performance compared to existing methods.
  • Further prospective, multi-institutional studies are warranted for validation.

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