Literature DB >> 23918528

Osteogenesis imperfecta in adults: phenotypic characteristics and response to treatment in an Irish cohort.

E S O'Sullivan1, S van der Kamp, M Kilbane, M McKenna.   

Abstract

BACKGROUND: Osteogenesis imperfecta (OI) is a heritable disorder of variable phenotype that is characterised by bone fragility and frequent fractures, with deformities and short stature in more severe cases. AIMS: We sought to review the response to treatment in a cohort of adult patients with OI.
METHODS: Charts of 16 patients with OI attending a metabolic bone disease clinic were reviewed, particularly with respect to the response to treatment using bisphosphonates and recombinant human parathyroid hormone (rhPTH). The response to treatment was assessed by monitoring bone mineral density (BMD) and bone turnover markers (BTMs).
RESULTS: In response to bisphosphonate therapy, median (range) BMD increased at the spine by 15.1(6.9-43.7) %. In response to rhPTH in 2 cases, spinal BMD increased by 40.3 and 27.2 %.
CONCLUSION: OI is debilitating disorder, but the course of the disease may be altered by treatment that increases BMD such as bisphosphonates and rhPTH. Both serial BMD and BTM aid in assessing response to intervention. Further study is needed with regard to fracture prevention.

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Year:  2013        PMID: 23918528     DOI: 10.1007/s11845-013-0995-x

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  24 in total

1.  Improving standards of DXA.

Authors:  M J McKenna; S van der Kamp; M Au-Yeong; O FitzGerald
Journal:  Ir Med J       Date:  2008-04

Review 2.  Classification of Osteogenesis Imperfecta revisited.

Authors:  F S Van Dijk; G Pals; R R Van Rijn; P G J Nikkels; J M Cobben
Journal:  Eur J Med Genet       Date:  2009-10-28       Impact factor: 2.708

3.  Children and adolescents treated with neridronate for osteogenesis imperfecta show no evidence of any osteonecrosis of the jaw.

Authors:  Evelina Maines; Elena Monti; Francesco Doro; Grazia Morandi; Paolo Cavarzere; Franco Antoniazzi
Journal:  J Bone Miner Metab       Date:  2011-11-08       Impact factor: 2.626

4.  Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.

Authors:  L M Ward; F Rauch; M P Whyte; J D'Astous; P E Gates; D Grogan; E L Lester; R E McCall; T A Pressly; J O Sanders; P A Smith; R D Steiner; E Sullivan; G Tyerman; D L Smith-Wright; N Verbruggen; N Heyden; A Lombardi; F H Glorieux
Journal:  J Clin Endocrinol Metab       Date:  2010-11-24       Impact factor: 5.958

5.  Radiological manifestations of bisphosphonate treatment with APD in a child suffering from osteogenesis imperfecta.

Authors:  J P Devogelaer; J Malghem; B Maldague; C Nagant de Deuxchaisnes
Journal:  Skeletal Radiol       Date:  1987       Impact factor: 2.199

Review 6.  Osteogenesis imperfecta.

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

Review 7.  Factors associated with osteonecrosis of the jaw among bisphosphonate users.

Authors:  Lisa M Hess; Joanne M Jeter; Marge Benham-Hutchins; David S Alberts
Journal:  Am J Med       Date:  2008-06       Impact factor: 4.965

8.  Risedronate in the treatment of mild pediatric osteogenesis imperfecta: a randomized placebo-controlled study.

Authors:  Frank Rauch; Craig F Munns; Christof Land; Moira Cheung; Francis H Glorieux
Journal:  J Bone Miner Res       Date:  2009-07       Impact factor: 6.741

Review 9.  Nosology and classification of genetic skeletal disorders: 2010 revision.

Authors:  Matthew L Warman; Valerie Cormier-Daire; Christine Hall; Deborah Krakow; Ralph Lachman; Martine LeMerrer; Geert Mortier; Stefan Mundlos; Gen Nishimura; David L Rimoin; Stephen Robertson; Ravi Savarirayan; David Sillence; Juergen Spranger; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

10.  A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.

Authors:  Oliver Semler; Lutz Garbes; Katharina Keupp; Daniel Swan; Katharina Zimmermann; Jutta Becker; Sandra Iden; Brunhilde Wirth; Peer Eysel; Friederike Koerber; Eckhard Schoenau; Stefan K Bohlander; Bernd Wollnik; Christian Netzer
Journal:  Am J Hum Genet       Date:  2012-08-02       Impact factor: 11.043

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  2 in total

Review 1.  Developments in rare bone diseases and mineral disorders.

Authors:  Siobhan Bacon; Rachel Crowley
Journal:  Ther Adv Chronic Dis       Date:  2017-11-24       Impact factor: 5.091

Review 2.  Recent developments in osteogenesis imperfecta.

Authors:  Joseph L Shaker; Carolyne Albert; Jessica Fritz; Gerald Harris
Journal:  F1000Res       Date:  2015-09-07
  2 in total

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