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Related Experiment Video

Updated: May 29, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
09:16

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Published on: June 30, 2018

Circulating endoglin concentration is not elevated in chronic kidney disease.

David M Charytan1, Alexander M Helfand, Brian A MacDonald

  • 1Renal Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, United States of America. dcharytan@partners.org

Plos One
|September 3, 2011
PubMed
Summary

Circulating soluble endoglin levels do not change with chronic kidney disease (CKD) severity. Therefore, soluble endoglin is unlikely to be a factor in CKD progression or cardiovascular disease risk in these patients.

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Area of Science:

  • Cardiovascular Physiology
  • Nephrology
  • Biomarker Research

Background:

  • Soluble endoglin, a transforming growth factor-beta (TGF-β) receptor, is crucial for cardiovascular health.
  • The relationship between soluble endoglin levels and chronic kidney disease (CKD) remains unclear.
  • It is unknown if elevated soluble endoglin contributes to cardiovascular mortality in CKD patients.

Purpose of the Study:

  • To investigate the association between circulating soluble endoglin concentrations and the presence and stage of CKD.
  • To determine if soluble endoglin levels are elevated in individuals with CKD.
  • To assess the potential role of soluble endoglin in CKD progression and associated cardiovascular risks.

Main Methods:

  • Serum endoglin levels were measured in 216 participants (118 with CKD stage 3+).
  • Estimated glomerular filtration rate (eGFR) and CKD stage were determined.
  • Univariate and multivariable regression analyses examined the association between eGFR, CKD stage, and soluble endoglin concentration.

Main Results:

  • Serum endoglin concentration did not significantly correlate with CKD stage (P=0.09) or eGFR (P=0.12).
  • Endoglin levels were similar in patients with end-stage renal disease (ESRD) and those with preserved renal function.
  • No significant association was found between endoglin concentration and urinary albumin excretion.

Conclusions:

  • Circulating soluble endoglin levels are not associated with renal function in patients.
  • Elevated soluble endoglin is unlikely to drive CKD progression.
  • Soluble endoglin does not appear to contribute to the heightened cardiovascular disease risk observed in individuals with CKD.