Author:
Miura Marina,Miura Yutaka,Iwazu Yoshitaka,Mukai Hideyuki,Sugiura Takahiro,Suzuki Yuji,Kato Masami,Kano Mayumi,Nagata Daisuke,Shiizaki Kazuhiro,Kurosu Hiroshi,Kuro-o Makoto
Abstract
AbstractHyperphosphatemia 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.
Funder
AMED-CREST
AMED-ACT-MS
AMED-ACT-M
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Cited by
4 articles.
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