Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29317
Title: Bisphosphonate therapy in CKD: The current state of affairs.
Authors: Nickolas T.L.;Damasiewicz M.J.
Monash Health Department(s): Nephrology
Institution: (Damasiewicz) Department of Nephrology, Monash Health, Monash University, Clayton, VIC, Australia (Damasiewicz) Department of Medicine, Monash University, Clayton, VIC, Australia (Nickolas) Division of Nephrology, Department of Medicine, Columbia University Medical Center, New York, NY, United States
Issue Date: 10-Mar-2020
Copyright year: 2020
Publisher: Lippincott Williams and Wilkins (E-mail: agents@lww.com)
Place of publication: United Kingdom
Publication information: Current Opinion in Nephrology and Hypertension. 29 (2) (pp 221-226), 2020. Date of Publication: 01 Mar 2020.
Journal: Current Opinion in Nephrology and Hypertension
Abstract: Purpose of reviewChronic kidney disease (CKD) is associated with the development of mineral and bone disorders (MBD), including renal osteodystrophy (ROD). ROD is a global disorder of bone strength that is associated with an increased fracture risk. The use of bisphosphonates for fracture risk reduction in CKD remains controversial. This review provides a synopsis of the state-of-the literature regarding the safety and potential antifracture benefits of bisphosphonates in CKD patients.Recent findingsIn preclinical studies of animals with CKD 3-4 and evidence of CKD-MBD, bisphosphonates resulted in changes in bone quality that improve bone strength. Bone turnover was generally reduced to a similar extent in animals with and without CKD. Post hoc analyses of randomized trials in patients with CKD 3-4 reported increases in bone mineral density (BMD) and fracture reduction that were similar in patients with and without CKD. There are no primary clinical trial data in patients with CKD-MBD.SummaryIn patients with CKD without evidence of CKD-MBD, the use of bisphosphonates should follow general population guidelines. The lack of data for patients with CKD 4-5D and evidence of CKD-MBD makes treatment decisions challenging. Clinical studies are urgently needed to provide data on the safety and antifracture benefits of bisphosphonates in these cohorts.Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1097/MNH.0000000000000585
PubMed URL: 31833938 [http://www.ncbi.nlm.nih.gov/pubmed/?term=31833938]
ISSN: 1062-4821
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/29317
Type: Review
Subjects: fracture
kidney injury
pharmacokinetic parameters
renal osteodystrophy
risk reduction
bisphosphonic acid derivative
bisphosphonic acid derivative/an [Drug Analysis]
osteoporosis
adverse drug reaction
bone density
bone disease
bone strength
bone turnover
chronic kidney disease-mineral and bone disorder
chronic kidney failure
clinical study
drug efficacy
drug mechanism
drug safety
drug structure
end stage renal disease
fracture
Type of Clinical Study or Trial: Review article (e.g. literature review, narrative review)
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