Bone Fracture in Rett Syndrome: Mechanisms and Prevention Strategies

Author:

Caffarelli Carla1ORCID,Al Refaie Antonella1,Mondillo Caterina1,De Vita Michela1,Baldassini Leonardo1,Valacchi Giuseppe23ORCID,Gonnelli Stefano1

Affiliation:

1. Department of Medicine, Surgery and Neuroscience, University of Siena, 53100 Siena, Italy

2. Department of Biomedical and Specialist Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy

3. Animal Science Department, Plants for Human Health Institute, North Carolina Research Campus, North Carolina State University, Kannapolis, NC 27695, USA

Abstract

The present study aimed to evaluate the burden and management of fragility fractures in subjects with Rett syndrome. We searched all relevant medical literature from 1 January 1986 to 30 June 2023 for studies under the search term “Rett syndrome and fracture”. The fracture frequency ranges from a minimum of 13.9% to a maximum of 36.1%. The majority of such fractures occur in lower limb bones and are associated with low bone mineral density. Anticonvulsant use, joint contractures, immobilization, low physical activity, poor nutrition, the genotype, and lower calcium and vitamin D intakes all significantly impair skeletal maturation and bone mass accrual in Rett syndrome patients, making them more susceptible to fragility fractures. This review summarizes the knowledge on risk factors for fragility fracture in patients with Rett syndrome and suggests a possible diagnostic and therapeutic care pathway for improving low bone mineral density and reducing the risk of fragility fractures. The optimization of physical activity, along with adequate nutrition and the intake of calcium and vitamin D supplements, should be recommended. In addition, subjects with Rett syndrome and a history of fracture should consider using bisphosphonates.

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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