Literature DB >> 27562566

Serum creatine kinase isoenzymes in children with osteogenesis imperfecta.

P D'Eufemia1, R Finocchiaro2, A Zambrano2, V Lodato2, L Celli2, S Finocchiaro2, P Persiani3, A Turchetti2, M Celli2.   

Abstract

This study evaluates serum creatine kinase isoenzyme activity in children with osteogenesis imperfecta to determine its usefulness as a biochemical marker during treatment with bisphosphonate. The changes of creatine kinase (CK) isoenzyme activity during and after discontinuation therapy were observed. These results could be useful in addressing over-treatment risk prevention.
INTRODUCTION: The brain isoenzyme of creatine kinase (CKbb) is highly expressed in mature osteoclasts during osteoclastogenesis, thus plays an important role in bone resorption. We previously identified high serum CKbb levels in 18 children with osteogenesis imperfect (OI) type 1 treated for 1 year with bisphosphonate (neridronate). In the present study, serum CK isoenzymes were evaluated in the same children with continuous versus discontinued neridronate treatment over a further 2-year follow-up period.
METHODS: This study included 18 children with OI type 1, 12 with continued (group A) and 6 with ceased (group B) neridronate treatment. Auxological data, serum biochemical markers of bone metabolism, bone mineral density z-score, and serum total CK and isoenzyme activities were determined in both groups.
RESULTS: Serum CKbb was progressively and significantly increased in group A (p < 0.004) but rapidly decreased to undetectable levels in group B. In both groups, the cardiac muscle creatine kinase isoenzyme (CKmb) showed a marked decrease, while serum C-terminal telopeptide (CTx) levels were almost unchanged.
CONCLUSIONS: This study provides evidence of the cumulative effect of neridronate administration in increasing serum CKbb levels and the reversible effect after its discontinuation. This approach could be employed for verifying the usefulness of serum CKbb as a biochemical marker in patients receiving prolonged bisphosphonate treatment. Moreover, the decreased serum CKmb levels suggest a systemic effect of these drugs.

Entities:  

Keywords:  Bisphosphonates; Bone metabolism; Creatine kinase isoenzymes; Osteoclast; Osteogenesis imperfecta

Mesh:

Substances:

Year:  2016        PMID: 27562566     DOI: 10.1007/s00198-016-3729-x

Source DB:  PubMed          Journal:  Osteoporos Int        ISSN: 0937-941X            Impact factor:   4.507


  26 in total

1.  IFCC primary reference procedures for the measurement of catalytic activity concentrations of enzymes at 37 degrees C. Part 2. Reference procedure for the measurement of catalytic concentration of creatine kinase.

Authors:  Gerhard Schumann; Roberto Bonora; Ferruccio Ceriotti; Pascale Clerc-Renaud; Carlo A Ferrero; Georges Férard; Paul F H Franck; F Javier Gella; Wieland Hoelzel; Poul Jørgen Jørgensen; Takashi Kanno; Art Kessne; Rainer Klauker; Nina Kristiansen; Jean-Marc Lessinger; Thomas P J Linsinger; Hideo Misaki; Mauro Panteghini; Jean Pauwels; Heinz G Schimmel; Arlette Vialle; Gerhard Weidemann; Lothar Siekmann
Journal:  Clin Chem Lab Med       Date:  2002-06       Impact factor: 3.694

2.  Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II.

Authors:  J Gram; S Antonsen; M Hørder; J Bollerslev
Journal:  Calcif Tissue Int       Date:  1991-06       Impact factor: 4.333

Review 3.  Bisphosphonates: effects on osteoblast.

Authors:  Nicola Maruotti; Addolorata Corrado; Anna Neve; Francesco Paolo Cantatore
Journal:  Eur J Clin Pharmacol       Date:  2012-02-09       Impact factor: 2.953

4.  Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders.

Authors:  M P Whyte; A Chines; D P Silva; Y Landt; J H Ladenson
Journal:  J Bone Miner Res       Date:  1996-10       Impact factor: 6.741

5.  RANKL up-regulates brain-type creatine kinase via poly(ADP-ribose) polymerase-1 during osteoclastogenesis.

Authors:  Jianfeng Chen; Yong Sun; Xia Mao; Qizhan Liu; Hui Wu; Yabing Chen
Journal:  J Biol Chem       Date:  2010-09-13       Impact factor: 5.157

6.  Intravenous neridronate in children with osteogenesis imperfecta: a randomized controlled study.

Authors:  Davide Gatti; Franco Antoniazzi; Rosangela Prizzi; Vania Braga; Maurizio Rossini; Luciano Tatò; Ombretta Viapiana; Silvano Adami
Journal:  J Bone Miner Res       Date:  2004-12-20       Impact factor: 6.741

Review 7.  The use of bisphosphonates in children with osteogenesis imperfecta.

Authors:  F H Glorieux
Journal:  J Pediatr Endocrinol Metab       Date:  2001       Impact factor: 1.634

Review 8.  Osteogenesis imperfecta.

Authors:  Frank Rauch; Francis H Glorieux
Journal:  Lancet       Date:  2004-04-24       Impact factor: 79.321

9.  Osteogenesis imperfecta: an expanding panorama of variants.

Authors:  D Sillence
Journal:  Clin Orthop Relat Res       Date:  1981-09       Impact factor: 4.176

10.  Serum brain-type creatine kinase increases in children with osteogenesis imperfecta during neridronate treatment.

Authors:  Patrizia D'Eufemia; Roberto Finocchiaro; Ciro Villani; Anna Zambrano; Valentina Lodato; Marta Palombaro; Enrico Properzi; Mauro Celli
Journal:  Pediatr Res       Date:  2014-02-11       Impact factor: 3.756

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  1 in total

1.  Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG).

Authors:  M Celli; P D'Eufemia; P Persiani; A Turchetti; A Febbo; Y D'Alfonso; L Celli; A Zambrano
Journal:  Osteoporos Int       Date:  2017-09-02       Impact factor: 4.507

  1 in total

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