Literature DB >> 21267600

Can bisphosphonates play a role in the treatment of children with chronic kidney disease?

Dieter Haffner1, Dagmar-Christiane Fischer.   

Abstract

In patients with chronic kidney disease (CKD) renal osteodystrophy, in the form of either low- or high-turnover bone disease, is quite common. While renal transplantation is expected to reverse renal osteodystrophy, long-term treatment with glucocorticoids before and/or after transplantation may lead to osteoporosis instead. Osteoporosis is defined as a skeletal disease with low bone mineral density, microarchitectural deterioration, and concomitant fragility. In adults, bisphosphonates are widely used to treat osteoporosis and other diseases associated with excessive bone resorption. In pediatric CKD patients the efficacy and safety of these drugs have not yet been addressed adequately and thus no evidence-based recommendations regarding the optimal type of bisphosphonate, dosage, or duration of therapy are available. Furthermore, while in adults the determination of areal bone mineral density is sufficient to diagnose osteoporosis, this is not the case in children. Instead, in pediatric patients, careful morphological assessment of bone structure and formation is required. Indeed, data from studies with uremic rats indicated that bisphosphonates, via a deceleration of bone turnover, have the potential not only to aggravate pre-existing adynamic bone disease, but also to impair longitudinal growth. Thus, the widespread use of bisphosphonates in children with CKD should be discouraged until the risks and benefits have been carefully elucidated in clinical trials.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21267600     DOI: 10.1007/s00467-010-1739-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  80 in total

Review 1.  Biochemical measurements of bone turnover in children and adolescents.

Authors:  P Szulc; E Seeman; P D Delmas
Journal:  Osteoporos Int       Date:  2000       Impact factor: 4.507

Review 2.  Clinical epidemiology of cardiovascular disease in chronic renal disease.

Authors:  R N Foley; P S Parfrey; M J Sarnak
Journal:  Am J Kidney Dis       Date:  1998-11       Impact factor: 8.860

Review 3.  Differences in nephrotoxicity of intravenous bisphosphonates for the treatment of malignancy-related bone disease.

Authors:  Raoul Bergner; Ingo J Diel; Dirk Henrich; Martin Hoffmann; Michael Uppenkamp
Journal:  Onkologie       Date:  2006-10-25

Review 4.  Effect of kidney transplantation on bone.

Authors:  K Kodras; M Haas
Journal:  Eur J Clin Invest       Date:  2006-08       Impact factor: 4.686

Review 5.  Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. Report of a WHO Study Group.

Authors: 
Journal:  World Health Organ Tech Rep Ser       Date:  1994

Review 6.  Glucocorticoid-induced osteoporosis in children: impact of the underlying disease.

Authors:  Mary B Leonard
Journal:  Pediatrics       Date:  2007-03       Impact factor: 7.124

7.  Ibandronate affects bone growth and mineralization in rats with normal and reduced renal function.

Authors:  Dagmar-Christiane Fischer; Claudia Jensen; Anja Rahn; Birgit Salewski; Günther Kundt; Geert J Behets; Patrick D'Haese; Dieter Haffner
Journal:  Pediatr Nephrol       Date:  2010-10-15       Impact factor: 3.714

8.  Removal of clodronate by haemodialysis in end-stage renal disease patients.

Authors:  A E Beigel; E Rienhoff; C J Olbricht
Journal:  Nephrol Dial Transplant       Date:  1995-12       Impact factor: 5.992

9.  Prevention of bone loss in renal transplant recipients: a prospective, randomized trial of intravenous pamidronate.

Authors:  Maria Coco; Daniel Glicklich; Marie Claude Faugere; Larry Burris; Istvan Bognar; Peter Durkin; Vivian Tellis; Stuart Greenstein; Richard Schechner; Katherine Figueroa; Patricia McDonough; Guodong Wang; Hartmut Malluche
Journal:  J Am Soc Nephrol       Date:  2003-10       Impact factor: 10.121

10.  Cardiovascular mortality in children and young adults with end-stage kidney disease.

Authors:  R S Parekh; C E Carroll; R A Wolfe; F K Port
Journal:  J Pediatr       Date:  2002-08       Impact factor: 4.406

View more
  4 in total

1.  Skeletal levels of bisphosphonate in the setting of chronic kidney disease are independent of remodeling rate and lower with fractionated dosing.

Authors:  Elizabeth A Swallow; Mohammad W Aref; Corinne E Metzger; Spencer Sacks; Demi R Lehmkuhler; Neal Chen; Max A Hammond; Paul R Territo; Thomas L Nickolas; Sharon M Moe; Matthew R Allen
Journal:  Bone       Date:  2019-07-09       Impact factor: 4.398

2.  Skeletal accumulation of fluorescently tagged zoledronate is higher in animals with early stage chronic kidney disease.

Authors:  E A Swallow; M W Aref; N Chen; I Byiringiro; M A Hammond; B P McCarthy; P R Territo; M M Kamocka; S Winfree; K W Dunn; S M Moe; M R Allen
Journal:  Osteoporos Int       Date:  2018-06-11       Impact factor: 4.507

3.  Pediatric CKD-MBD: existing and emerging treatment approaches.

Authors:  Rose M Ayoob; John D Mahan
Journal:  Pediatr Nephrol       Date:  2022-01-17       Impact factor: 3.651

4.  Treatment of adynamic bone disease in a haemodialysis patient with teriparatide.

Authors:  Panagiotis Giamalis; Dominiki Economidou; Chrysostomos Dimitriadis; Dimitrios Memmos; Aikaterini Papagianni; Georgios Efstratiadis
Journal:  Clin Kidney J       Date:  2015-02-10
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.