Clinical Utility of Bone Turnover Markers in Chronic Kidney Disease

dc.contributor.authorSrisuwarn P.
dc.contributor.authorEastell R.
dc.contributor.authorSalam S.
dc.contributor.correspondenceSrisuwarn P.
dc.contributor.otherMahidol University
dc.date.accessioned2024-12-28T18:04:16Z
dc.date.available2024-12-28T18:04:16Z
dc.date.issued2024-11-01
dc.description.abstractChronic kidney disease (CKD) often leads to mineral and bone disorders (CKD-MBDs), which are nearly universal in patients undergoing dialysis. CKD-MBD includes abnormal calcium-phosphate metabolism, vascular and soft tissue calcification, and bone abnormalities (renal osteodystrophy [ROD]). Bone fragility in CKD occurs due to low bone mass and poor bone quality, and patients with CKD have higher fracture and mortality rates. Bone histomorphometry is the gold standard for ROD diagnosis; however, it is labor-intensive and expensive. The Kidney Disease Improving Global Outcomes clinical practice guidelines on CKD-MBD suggest serum parathyroid hormone (PTH) and bone-specific alkaline phosphatase (bone ALP) for predicting bone turnover in ROD. In this review, we focus on the role of PTH and bone turnover markers, intact procollagen type N-terminal propeptide of type I collagen, bone ALP, and tartrate-resistant acid phosphatase 5b in diagnosing ROD, predicting fractures, and guiding treatment in patients with CKD.
dc.identifier.citationJournal of Bone Metabolism Vol.31 No.4 (2024) , 264-278
dc.identifier.doi10.11005/jbm.24.789
dc.identifier.eissn22877029
dc.identifier.issn22876375
dc.identifier.scopus2-s2.0-85212606911
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/102543
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.titleClinical Utility of Bone Turnover Markers in Chronic Kidney Disease
dc.typeReview
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85212606911&origin=inward
oaire.citation.endPage278
oaire.citation.issue4
oaire.citation.startPage264
oaire.citation.titleJournal of Bone Metabolism
oaire.citation.volume31
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationSheffield Teaching Hospitals NHS Foundation Trust
oairecerif.author.affiliationThe University of Sheffield

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