Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/18543
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dc.contributor.authorRroji, Meritaen_US
dc.contributor.authorFigurek, Andrejaen_US
dc.contributor.authorSpasovski, Goceen_US
dc.date.accessioned2022-06-13T08:06:13Z-
dc.date.available2022-06-13T08:06:13Z-
dc.date.issued2020-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/18543-
dc.description.abstractCardiovascular (CV) disease is highly prevalent in the population with chronic kidney disease (CKD), where the risk of CV death in early stages far exceeds the risk of progression to dialysis. The presence of chronic kidney disease-mineral and bone disorder (CKD-MBD) has shown a strong correlation with CV events and mortality. As a non-atheromatous process, it could be partially explained why standard CV disease-modifying drugs do not provide such an impact on CV mortality in CKD as observed in the general population. We summarize the potential association of CV comorbidities with the older (parathyroid hormone, phosphate) and newer (FGF23, Klotho, sclerostin) CKD-MBD biomarkers.en_US
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.relation.ispartofToxinsen_US
dc.titleShould We Consider the Cardiovascular System While Evaluating CKD-MBD?en_US
dc.typeArticleen_US
dc.identifier.doi10.3390/toxins12030140-
dc.identifier.urlhttps://www.mdpi.com/2072-6651/12/3/140/pdf-
dc.identifier.volume12-
dc.identifier.issue3-
item.grantfulltextopen-
item.fulltextWith Fulltext-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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