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https://repository.monashhealth.org/monashhealthjspui/handle/1/29317Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Nickolas T.L. | en |
| dc.contributor.author | Damasiewicz M.J. | en |
| dc.date.accessioned | 2021-05-14T09:54:18Z | en |
| dc.date.available | 2021-05-14T09:54:18Z | en |
| dc.date.copyright | 2020 | en |
| dc.date.created | 20200310 | en |
| dc.date.issued | 2020-03-10 | en |
| dc.identifier.citation | Current Opinion in Nephrology and Hypertension. 29 (2) (pp 221-226), 2020. Date of Publication: 01 Mar 2020. | en |
| dc.identifier.issn | 1062-4821 | en |
| dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/29317 | en |
| dc.description.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. | en |
| dc.language | English | en |
| dc.language | en | en |
| dc.publisher | Lippincott Williams and Wilkins (E-mail: agents@lww.com) | en |
| dc.relation.ispartof | Current Opinion in Nephrology and Hypertension | en |
| dc.subject.mesh | fracture | - |
| dc.subject.mesh | kidney injury | - |
| dc.subject.mesh | pharmacokinetic parameters | - |
| dc.subject.mesh | renal osteodystrophy | - |
| dc.subject.mesh | risk reduction | - |
| dc.subject.mesh | bisphosphonic acid derivative | - |
| dc.subject.mesh | bisphosphonic acid derivative/an [Drug Analysis] | - |
| dc.subject.mesh | osteoporosis | - |
| dc.subject.mesh | adverse drug reaction | - |
| dc.subject.mesh | bone density | - |
| dc.subject.mesh | bone disease | - |
| dc.subject.mesh | bone strength | - |
| dc.subject.mesh | bone turnover | - |
| dc.subject.mesh | chronic kidney disease-mineral and bone disorder | - |
| dc.subject.mesh | chronic kidney failure | - |
| dc.subject.mesh | clinical study | - |
| dc.subject.mesh | drug efficacy | - |
| dc.subject.mesh | drug mechanism | - |
| dc.subject.mesh | drug safety | - |
| dc.subject.mesh | drug structure | - |
| dc.subject.mesh | end stage renal disease | - |
| dc.subject.mesh | fracture | - |
| dc.title | Bisphosphonate therapy in CKD: The current state of affairs. | en |
| dc.type | Review | en |
| dc.identifier.affiliation | Nephrology | - |
| dc.type.studyortrial | Review article (e.g. literature review, narrative review) | - |
| dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1097/MNH.0000000000000585 | - |
| dc.publisher.place | United Kingdom | en |
| dc.identifier.pubmedid | 31833938 [http://www.ncbi.nlm.nih.gov/pubmed/?term=31833938] | en |
| dc.identifier.source | 631085057 | en |
| dc.identifier.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 | en |
| dc.description.address | T.L. Nickolas, Medicine, Columbia University Irving Medical Center, 622 west 168th Street, PH2-124, New York, NY 10032, United States. E-mail: tln2001@cumc.columbia.edu | en |
| dc.description.publicationstatus | Embase | en |
| dc.rights.statement | Copyright 2020 Elsevier B.V., All rights reserved. | en |
| dc.subect.keywords | Bisphosphonates Chronic kidney disease Chronic kidney disease- mineral and bone disorders End-stage kidney disease Fractures Osteoporosis | en |
| dc.identifier.authoremail | Nickolas T.L.; tln2001@cumc.columbia.edu | en |
| dc.description.grant | No: R01DK110871 Organization: (NIH) *National Institutes of Health* Organization No: 100000002 Country: United States No: R01DK119266 Organization: (NIH) *National Institutes of Health* Organization No: 100000002 Country: United States | en |
| item.openairetype | Review | - |
| item.fulltext | No Fulltext | - |
| item.grantfulltext | none | - |
| item.cerifentitytype | Publications | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| Appears in Collections: | Articles | |
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