Literature DB >> 27448250

Fracture Rates and Fracture Sites in Patients With Osteogenesis Imperfecta: A Nationwide Register-Based Cohort Study.

Lars Folkestad1,2,3, Jannie Dahl Hald4, Annette Kjaer Ersbøll5, Jeppe Gram3, Anne Pernille Hermann1, Bente Langdahl4, Bo Abrahamsen2,6,7, Kim Brixen2.   

Abstract

Osteogenesis imperfecta (OI) is a hereditary, clinically heterogeneous, connective tissue disorder. The population prevalence of OI in Denmark is 10.6 in 100,000. A hallmark of the disease is frequent fractures that are often precipitated by minimal trauma. The aim of the current study was to compare the fracture rates across the lifespan of patients with OI with that of a reference population from the general population. The present study was a Danish nationwide, population-based, cohort study using register data. We identified 644 (55.6% females) patients in the OI cohort through the Danish National Patient Register and 3361 (55.2% females) persons, randomly selected from the Civil Registry System. A total of 416 patients with OI experienced a total of 1566 fractures during the observation period of median 17.9 years (interquartile range [IQR], 12.4 to 18.0 years), summing to 10137 person years. In comparison, 709 persons in the reference population experienced a total of 1018 fractures during follow-up. Both male and female patients with OI had an increased fracture rate throughout their life. The fracture rate ratio for participants aged 0 to 19 years was 10.7, for participants aged 20 to 54 years 17.2, and for participants aged 55 years and over 4.1 when compared to the reference population. The highest fracture rate was seen in males with OI aged 0 to 19 years (257 fractures per 1000 person-years). The fractures appear to follow the same pattern as in the general population, with a peak during the toddler and adolescent years (incidence rate [IR] 233.9 per 1000 person years), fewer fractures during adulthood (IR 84.5 per 1000 person years), and increased fracture rates in older women (IR 111.9 per 1000 person years). This is the largest register-based nationwide study on the fracture epidemiology of patients with OI. The risk of fractures seems largest in the childhood and adolescent years, and the relative risk of fracture declines with age in patients with OI compared to the general population.
© 2016 American Society for Bone and Mineral Research. © 2016 American Society for Bone and Mineral Research.

Entities:  

Keywords:  COLLAGEN; EPIDEMIOLOGY; FRACTURE RATES; OSTEOGENESIS IMPERFECTA; RARE BONE DISEASES; REGISTER-BASED STUDIES

Mesh:

Year:  2016        PMID: 27448250     DOI: 10.1002/jbmr.2920

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  28 in total

1.  Finite element analysis of bone strength in osteogenesis imperfecta.

Authors:  Peter Varga; Bettina M Willie; Chris Stephan; Kenneth M Kozloff; Philippe K Zysset
Journal:  Bone       Date:  2020-01-22       Impact factor: 4.398

2.  Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta.

Authors:  Masaki Matsushita; Kenichi Mishima; Satoshi Yamashita; Nobuhiko Haga; Sayaka Fujiwara; Keiichi Ozono; Takuo Kubota; Taichi Kitaoka; Naoki Ishiguro; Hiroshi Kitoh
Journal:  J Bone Miner Metab       Date:  2019-08-13       Impact factor: 2.626

3.  Long-term follow-up in osteogenesis imperfecta type VI.

Authors:  P Trejo; T Palomo; K Montpetit; F Fassier; A Sato; F H Glorieux; F Rauch
Journal:  Osteoporos Int       Date:  2017-07-09       Impact factor: 4.507

Review 4.  Genetic causes and mechanisms of Osteogenesis Imperfecta.

Authors:  Joohyun Lim; Ingo Grafe; Stefanie Alexander; Brendan Lee
Journal:  Bone       Date:  2017-02-15       Impact factor: 4.398

5.  Combined technique of titanium telescopic rods and external fixation in osteogenesis imperfecta patients: First 12 consecutive cases.

Authors:  Dmitry Popkov; Tamara Dolganova; Eduard Mingazov; Dmitry Dolganov; Andrey Kobyzev
Journal:  J Orthop       Date:  2020-06-20

6.  Long Bone Fractures in Fibrous Dysplasia/McCune-Albright Syndrome: Prevalence, Natural History, and Risk Factors.

Authors:  Raya E S Geels; Maartje E Meier; Amanda Saikali; Roula Tsonaka; Natasha M Appelman-Dijkstra; Alison M Boyce
Journal:  J Bone Miner Res       Date:  2021-11-17       Impact factor: 6.390

7.  Osteogenesis imperfecta and the teeth, eyes, and ears-a study of non-skeletal phenotypes in adults.

Authors:  J D Hald; L Folkestad; C Z Swan; J Wanscher; M Schmidt; H Gjørup; D Haubek; C-H Leonhard; D A Larsen; J Ø Hjortdal; T Harsløf; M Duno; A M Lund; J-E B Jensen; K Brixen; B Langdahl
Journal:  Osteoporos Int       Date:  2018-08-24       Impact factor: 4.507

Review 8.  Muscle-Bone Interactions in Pediatric Bone Diseases.

Authors:  Louis-Nicolas Veilleux; Frank Rauch
Journal:  Curr Osteoporos Rep       Date:  2017-10       Impact factor: 5.096

9.  Skeletal muscle specific mitochondrial dysfunction and altered energy metabolism in a murine model (oim/oim) of severe osteogenesis imperfecta.

Authors:  Victoria L Gremminger; Emily N Harrelson; Tara K Crawford; Adrienne Ohler; Laura C Schulz; R Scott Rector; Charlotte L Phillips
Journal:  Mol Genet Metab       Date:  2021-02-20       Impact factor: 4.797

10.  Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant

Authors:  Nidhi Gupta; Seth W. Gregory; David R. Deyle; Peter J. Tebben
Journal:  J Clin Res Pediatr Endocrinol       Date:  2020-06-10
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