Prevalence and Hospital Admissions in Patients With Osteogenesis Imperfecta in The Netherlands: A Nationwide Registry Study

Osteogenesis Imperfecta (OI) is a complex disease caused by genetic alterations in production of collagen type I, and collagen-related proteins. Bone fragility is the most common patient issue, but extraskeletal complications also present an adverse factor in the quality of life and prognosis of patients with OI. However, still little is known about the morbidity and mortality of these patients. The objective of this paper is to determine and describe to what extent OI impacts patients’ life in terms of hospitalization and complications describing the incidence and prevalence of the Dutch cohort of OI patients and the characteristics of their hospital admissions. Information regarding OI patients and their hospital admission was extracted from the Statistics Netherlands Database and matched to the OI Genetics Database of Amsterdam UMC. Hospital admission data was available for 674 OI patients. This OI nationwide registry study shows that the life expectancy of OI patients is adversely affected by the disease. The median annual incidence risk of OI between 1992 and 2019 was 6.5 per 100,000 live births. Furthermore, patients with OI had a 2.9 times higher hospitalization rate compared to the general Dutch population. The highest hospitalization rate ratio of 8.4 was reported in the patient group between 0 and 19 years old. OI type and severity had impact on extraskeletal manifestations, which play a key role in the numerous hospital admissions. More awareness about the impact of OI on patients’ life is needed to improve and implement prevention and follow-up guidelines.

[1]  H. Weinans,et al.  Fractures in Osteogenesis Imperfecta: Pathogenesis, Treatment, Rehabilitation and Prevention , 2022, Children.

[2]  G. Pals,et al.  Collagen transport and related pathways in Osteogenesis Imperfecta , 2021, Human Genetics.

[3]  M. Javaid,et al.  Hospital admissions of patients with osteogenesis imperfecta in the English NHS , 2020, Osteoporosis International.

[4]  G. Janus,et al.  A Baseline Measurement of Quality of Life in 322 Adults With Osteogenesis Imperfecta , 2020, JBMR plus.

[5]  J. Darbà,et al.  Hospital incidence, management and direct cost of osteogenesis imperfecta in Spain: a retrospective database analysis , 2020, Journal of medical economics.

[6]  A. Ersbøll,et al.  Fracture Rates and Fracture Sites in Patients With Osteogenesis Imperfecta: A Nationwide Register‐Based Cohort Study , 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[7]  A. Hermann,et al.  Mortality and Causes of Death in Patients With Osteogenesis Imperfecta: A Register‐Based Nationwide Cohort Study , 2016, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[8]  A. Forlino,et al.  Osteogenesis imperfecta , 2016, The Lancet.

[9]  R. Arnold Retrospective Database Analysis , 2016 .

[10]  D. Sillence,et al.  Erratum to: Osteogenesis imperfecta: Clinical diagnosis, nomenclature, and severity assessment , 2015, American Journal of Medical Genetics. Part a.

[11]  D. Sillence,et al.  Osteogenesis imperfecta: Clinical diagnosis, nomenclature and severity assessment , 2014, American journal of medical genetics. Part A.

[12]  P. Byers,et al.  Osteogenesis imperfecta , 2012, Nature Reviews Disease Primers.

[13]  Elena Monti,et al.  Current and emerging treatments for the management of osteogenesis imperfecta , 2010, Therapeutics and clinical risk management.

[14]  M. Vitale,et al.  Osteogenesis Imperfecta: Determining the Demographics and the Predictors of Death From an Inpatient Population , 2007, Journal of pediatric orthopedics.

[15]  C. Paterson,et al.  Causes of death in osteogenesis imperfecta. , 1996, Journal of clinical pathology.

[16]  S. Ogston,et al.  Life expectancy in osteogenesis imperfecta , 1995, BMJ.

[17]  D. Sillence,et al.  Genetic heterogeneity in osteogenesis imperfecta. , 1979, Journal of medical genetics.

[18]  G. Pals,et al.  Classification of Osteogenesis Imperfecta revisited. , 2010, European journal of medical genetics.

[19]  R. B. Singer,et al.  Mortality in various types of osteogenesis imperfecta. , 2001, Journal of insurance medicine.

[20]  W. Cole Osteogenesis imperfecta. , 1988, Bailliere's clinical endocrinology and metabolism.

[21]  D. Sillence,et al.  Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. , 1979, Birth defects original article series.