AI Article Synopsis

  • - Hyperphosphatemia in patients with end-stage renal disease is linked to poor health outcomes, but the exact molecular mechanisms involved are not well understood.
  • - Research suggests that calciprotein particles (CPPs), linked to high serum phosphorus levels, may contribute to health issues by causing calcification and inflammation in blood vessels.
  • - A study using hyperphosphatemic pigs showed that removing CPPs from the blood with a special adsorption column improved survival and reduced complications, highlighting CPPs as a potential target for new treatments in hemodialysis patients.

Article Abstract

Hyperphosphatemia is a major risk for poor prognosis in patients with end-stage renal disease. However, the molecular mechanism behind this link remains elusive. We and others have demonstrated that serum phosphorus levels correlate positively with circulating levels of calciprotein particles (CPPs). CPPs are colloidal mineral-protein complexes containing insoluble calcium-phosphate precipitates and have been reported to induce calcification in cultured vascular smooth muscle cells and inflammatory responses in cultured macrophages. Hence, we hypothesize that CPPs may be responsible for disorders associated with hyperphosphatemia. Using hyperphosphatemic miniature pigs receiving hemodialysis, here we show that removal of CPPs from the blood with a newly developed CPP adsorption column improves survival and alleviates complications including coronary artery calcification, vascular endothelial dysfunction, metastatic pulmonary calcification, left ventricular hypertrophy, and chronic inflammation. The present study identifies CPPs as an effective therapeutic target and justifies clinical trials to determine whether the CPP adsorption column may be useful as a medical device for improving clinical outcomes of hemodialysis patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497634PMC
http://dx.doi.org/10.1038/s41598-023-42273-0DOI Listing

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