Literature DB >> 26856585

Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α.

G Brunetti1, F Papadia2, A Tummolo2, R Fischetto2, F Nicastro2, L Piacente3, A Ventura3, G Mori4, A Oranger5, I Gigante5, S Colucci5, M Ciccarelli3, M Grano5, L Cavallo3, M Delvecchio3, M F Faienza6.   

Abstract

UNLABELLED: In this study, we investigated the bone cell activity in patients with osteogenesis imperfecta (OI) treated and untreated with neridronate. We demonstrated the key role of Dickkopf-1 (DKK1), receptor activator of nuclear factor-κB ligand (RANKL), and tumor necrosis factor alpha (TNF-α) in regulating bone cell of untreated and treated OI subjects. These cytokines could represent new pharmacological targets for OI.
INTRODUCTION: Bisphosphonates are widely used in the treatment of children with osteogenesis imperfecta (OI) with the objective of reducing the risk of fractures. Although bisphosphonates increase bone mineral density in OI subjects, the effects on fracture incidence are conflicting. The aim of this study was to investigate the mechanisms underlying bone cell activity in subjects with mild untreated forms of OI and in a group of subjects with severe OI treated with cycles of intravenous neridronate.
METHODS: Sclerostin, DKK1, TNF-α, RANKL, osteoprotegerin (OPG), and bone turnover markers were quantified in serum of 18 OI patients (12 females, mean age 8.86 ± 3.90), 8 of which were receiving cyclic intravenous neridronate, and 21 sex- and age-matched controls. The effects on osteoblastogenesis and OPG expression of media conditioned by the serum of OI patients and anti-DKK1 neutralizing antibody were evaluated. Osteoclastogenesis was assessed in cultures from patients and controls.
RESULTS: DKK1 and RANKL levels were significantly increased both in untreated and in treated OI subjects with respect to controls. The serum from patients with high DKK1 levels inhibited both osteoblast differentiation and OPG expression in vitro. High RANKL and low OPG messenger RNA (mRNA) levels were found in lymphomonocytes from patients. High amounts of TNF-α were expressed by monocytes, and an elevated percentage of circulating CD11b-CD51/CD61+ osteoclast precursors was observed in patients.
CONCLUSIONS: Our study demonstrated the key role of DKK1, RANKL, and TNF-α in regulating bone cell activity of subjects with OI untreated and treated with bisphosphonates. These cytokines could represent new pharmacological targets for OI patients.

Entities:  

Keywords:  DKK1; Osteoblasts; Osteoclasts; Osteogenesis imperfecta; RANKL

Mesh:

Substances:

Year:  2016        PMID: 26856585     DOI: 10.1007/s00198-016-3501-2

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


  44 in total

1.  Deletion of a single allele of the Dkk1 gene leads to an increase in bone formation and bone mass.

Authors:  Frederic Morvan; Kim Boulukos; Philippe Clément-Lacroix; Sergio Roman Roman; Isabelle Suc-Royer; Béatrice Vayssière; Patrick Ammann; Patrick Martin; Sonia Pinho; Philippe Pognonec; Patrick Mollat; Christof Niehrs; Roland Baron; Georges Rawadi
Journal:  J Bone Miner Res       Date:  2006-06       Impact factor: 6.741

2.  Sclerostin binds to LRP5/6 and antagonizes canonical Wnt signaling.

Authors:  Xiaofeng Li; Yazhou Zhang; Heeseog Kang; Wenzhong Liu; Peng Liu; Jianghong Zhang; Stephen E Harris; Dianqing Wu
Journal:  J Biol Chem       Date:  2005-03-18       Impact factor: 5.157

3.  In patients with rheumatoid arthritis, Dickkopf-1 serum levels are correlated with parathyroid hormone, bone erosions and bone mineral density.

Authors:  Maurizio Rossini; Ombretta Viapiana; Silvano Adami; Elena Fracassi; Luca Idolazzi; Carmela Dartizio; Maria Rosaria Povino; Giovanni Orsolini; Davide Gatti
Journal:  Clin Exp Rheumatol       Date:  2014-12-01       Impact factor: 4.473

4.  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

5.  Comparable outcomes in fracture reduction and bone properties with RANKL inhibition and alendronate treatment in a mouse model of osteogenesis imperfecta.

Authors:  R Bargman; R Posham; A L Boskey; E DiCarlo; C Raggio; N Pleshko
Journal:  Osteoporos Int       Date:  2011-09-08       Impact factor: 4.507

6.  Osteoblastic response to the defective matrix in the osteogenesis imperfecta murine (oim) mouse.

Authors:  I Kalajzic; J Terzic; Z Rumboldt; K Mack; A Naprta; F Ledgard; G Gronowicz; S H Clark; D W Rowe
Journal:  Endocrinology       Date:  2002-05       Impact factor: 4.736

7.  High levels of serum prostaglandin E2 in children with osteogenesis imperfecta are reduced by neridronate treatment.

Authors:  Patrizia D'Eufemia; Roberto Finocchiaro; Mauro Celli; Anna Zambrano; Martina Tetti; Ciro Villani; Pietro Persiani; Emanuela Mari; Alessandra Zicari
Journal:  Pediatr Res       Date:  2008-02       Impact factor: 3.756

8.  Kremen proteins are Dickkopf receptors that regulate Wnt/beta-catenin signalling.

Authors:  Bingyu Mao; Wei Wu; Gary Davidson; Joachim Marhold; Mingfa Li; Bernard M Mechler; Hajo Delius; Dana Hoppe; Peter Stannek; Carmen Walter; Andrei Glinka; Christof Niehrs
Journal:  Nature       Date:  2002-05-26       Impact factor: 49.962

Review 9.  Recessive osteogenesis imperfecta: clinical, radiological, and molecular findings.

Authors:  Marianne Rohrbach; Cecilia Giunta
Journal:  Am J Med Genet C Semin Med Genet       Date:  2012-07-12       Impact factor: 3.908

Review 10.  Bisphosphonate therapy in pediatric patients.

Authors:  Guiti Eghbali-Fatourechi
Journal:  J Diabetes Metab Disord       Date:  2014-12-17
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  23 in total

Review 1.  Growth plate gene involment and isolated short stature.

Authors:  Maria Felicia Faienza; Mariangela Chiarito; Giacomina Brunetti; Gabriele D'Amato
Journal:  Endocrine       Date:  2020-06-05       Impact factor: 3.633

2.  Hypocalcemia following Neridronate Administration in Pediatric Patients with Osteogenesis Imperfecta: A Prospective Observational Study.

Authors:  Evelina Maines; Elisa Tadiotto; Grazia Morandi; Michela Fedrizzi; Rossella Gaudino; Paolo Cavarzere; Alessandra Guzzo; Franco Antoniazzi
Journal:  J Pediatr Genet       Date:  2020-01-06

3.  Circulating levels of dickkopf-1, osteoprotegerin and sclerostin are higher in old compared with young men and women and positively associated with whole-body bone mineral density in older adults.

Authors:  J Coulson; L Bagley; Y Barnouin; S Bradburn; G Butler-Browne; H Gapeyeva; J-Y Hogrel; T Maden-Wilkinson; A B Maier; C Meskers; C Murgatroyd; M Narici; M Pääsuke; L Sassano; S Sipilä; N Al-Shanti; L Stenroth; D A Jones; J S McPhee
Journal:  Osteoporos Int       Date:  2017-06-05       Impact factor: 4.507

4.  Molecular diagnosis in children with fractures but no extraskeletal signs of osteogenesis imperfecta.

Authors:  G Bardai; L M Ward; P Trejo; P Moffatt; F H Glorieux; F Rauch
Journal:  Osteoporos Int       Date:  2017-04-04       Impact factor: 4.507

5.  Efficacy of teriparatide vs neridronate in adults with osteogenesis imperfecta type I: a prospective randomized international clinical study.

Authors:  Paolo Tranquilli Leali; Massimo Balsano; Gianluca Maestretti; Matteo Brusoni; Veronica Amorese; Emanuele Ciurlia; Matteo Andreozzi; Gianfilippo Caggiari; Carlo Doria
Journal:  Clin Cases Miner Bone Metab       Date:  2017-10-25

6.  Splenomegaly, myeloid lineage expansion and increased osteoclastogenesis in osteogenesis imperfecta murine.

Authors:  Brya G Matthews; Emilie Roeder; Xi Wang; Hector Leonardo Aguila; Sun-Kyeong Lee; Danka Grcevic; Ivo Kalajzic
Journal:  Bone       Date:  2017-06-07       Impact factor: 4.398

7.  The use of quantitative ultrasound in a tertiary-level children hospital: role in the follow-up of chronically ill patients.

Authors:  Albina Tummolo; Giacomina Brunetti; Mario Giordano; Vincenza Carbone; Maria Felicia Faienza; Maurizio Aricò; Sabino Pesce
Journal:  J Ultrasound       Date:  2022-01-29

8.  An update on the role of RANKL-RANK/osteoprotegerin and WNT-ß-catenin signaling pathways in pediatric diseases.

Authors:  Giacomina Brunetti; Gabriele D'Amato; Mariangela Chiarito; Apollonia Tullo; Graziana Colaianni; Silvia Colucci; Maria Grano; Maria Felicia Faienza
Journal:  World J Pediatr       Date:  2018-10-20       Impact factor: 2.764

9.  Increased Osteocyte Lacunae Density in the Hypermineralized Bone Matrix of Children with Osteogenesis Imperfecta Type I.

Authors:  Matthias Mähr; Stéphane Blouin; Martina Behanova; Barbara M Misof; Francis H Glorieux; Jochen Zwerina; Frank Rauch; Markus A Hartmann; Nadja Fratzl-Zelman
Journal:  Int J Mol Sci       Date:  2021-04-26       Impact factor: 5.923

10.  Impact of Genetic and Pharmacologic Inhibition of Myostatin in a Murine Model of Osteogenesis Imperfecta.

Authors:  Catherine L Omosule; Victoria L Gremminger; Ashley M Aguillard; Youngjae Jeong; Emily N Harrelson; Lawrence Miloscio; Jason Mastaitis; Ashique Rafique; Sandra Kleiner; Ferris M Pfeiffer; Anqing Zhang; Laura C Schulz; Charlotte L Phillips
Journal:  J Bone Miner Res       Date:  2020-12-18       Impact factor: 6.741

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