An Instrument to Measure Skeletal Burden and Predict Functional Outcome in Fibrous Dysplasia of Bone
- 1 February 2005
- journal article
- Published by Oxford University Press (OUP) in Journal of Bone and Mineral Research
- Vol. 20 (2) , 219-226
- https://doi.org/10.1359/jbmr.041111
Abstract
An instrument to measure skeletal burden in fibrous dysplasia was developed. Biological and clinical relevance was shown by correlating skeletal burden scores with bone markers, quality of life, and ambulatory status. Childhood scores predict adult ambulatory status, and scores were unaffected when bone markers decreased with bisphosphonate treatment or aging. Introduction: Fibrous dysplasia (FD) is a skeletal disease with a broad clinical expression. There is no objective method to assess the extent of skeletal involvement or predict outcome. We developed an instrument to measure skeletal burden that correlates with physical function, health-related quality of life (HRQL), and ambulatory status. Materials and Methods: Seventy-nine patients with FD underwent bone scintigraphy. The skeletal burden score was derived from a weighted score based on the regional measurement using bone scintigraphy to estimate the amount of FD in anatomical segments. Six readers scored 20 scans twice to determine the inter- and intrareader agreement. To assess biological significance, scores were correlated with bone markers. To assess functional outcome, scores on the SF-36 (adults) or CHQ-PF50 (children) were correlated with skeletal burden scores. In a group of patients who had bone scans as children and adults (n = 6), the ability to predict ambulatory status was tested. Skeletal burden scores were assessed in patients before and after treatment with pamidronate (n = 5). Results: The inter- and intrareader agreement of burden scores were r = 0.96, and 0.98, respectively (p < 0.001 for both). The scores correlated with markers of bone metabolism and HRQL (Spearman rho, 0.54-0.67 p < 0.001 and −0.43, p = 0.001, respectively). The mean score of patients who ambulated unassisted was significantly lower than those requiring assistance (p < 0.001 unassisted versus crutch and/or wheelchair). In unassisted ambulators, younger patients had higher scores, suggesting high childhood scores may predict adulthood impairment. In six patients with childhood and adulthood scans, childhood scores >30 predicted assisted ambulation in adulthood. There was a negative correlation between bone markers and age (Spearman rho, −0.42 to −0.70; p < 0.001), but not age and skeletal burden score. Pamidronate treatment decreased serum alkaline phosphatase but had no effect on the skeletal burden score. Conclusions: This is a validated and reliable instrument for the measurement of skeletal burden of FD and is able to predict functional outcome.Keywords
This publication has 15 references indexed in Scilit:
- Fracture Incidence in Polyostotic Fibrous Dysplasia and the McCune-Albright SyndromeJournal of Bone and Mineral Research, 2004
- Renal Phosphate Wasting in Fibrous Dysplasia of Bone Is Part of a Generalized Renal Tubular Dysfunction Similar to That Seen in Tumor-Induced OsteomalaciaJournal of Bone and Mineral Research, 2001
- Fibrous dysplasia of boneBest Practice & Research Clinical Rheumatology, 2000
- Mutations of the GNAS1 Gene, Stromal Cell Dysfunction, and Osteomalacic Changes in Non–McCune–Albright Fibrous Dysplasia of BoneJournal of Bone and Mineral Research, 2000
- Quantitative evaluation of bone scintigraphy in the assessment of Pagetʼs disease activityNuclear Medicine Communications, 1999
- McCune-Albright syndrome: new insightsCurrent Opinion in Endocrinology, Diabetes and Obesity, 1999
- A new method for assessing 99Tcm-MDP bone uptake from a bone scan imageNuclear Medicine Communications, 1992
- Activating Mutations of the Stimulatory G Protein in the McCune–Albright SyndromeNew England Journal of Medicine, 1991
- Benign bone tumorsSeminars in Nuclear Medicine, 1976
- Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in FemalesNew England Journal of Medicine, 1937