Affiliation:
1. 1. Medizinische Abteilung, Hanusch-Krankenhaus, Wien,
Austria
Abstract
AbstractDespite having different aetiologies, different rare bone diseases (RBDs) such as
hypophosphatasia (HPP), autosomal dominant hypophosphatemic rickets (ADHR),
X-linked hypophosphatemia (XLH) and osteogenesis imperfecta (OI) share common
clinical features such as growth disturbances, pathological fractures,
pseudo-fractures and chronic musculoskeletal pain. The role of micronutrients
including minerals, trace elements and vitamin D in the physiological bone
metabolism are well established. A significant share of RBD patients suffer from
nutritional deficiencies due to the underlying disease or do not achieve the
recommended daily intake (RDI) for micronutrients. The supplementation of
micronutrients in RBDs should have the goal of achieving the RDI and promoting
bone metabolism without increasing the burden of disease. Specific diets and an
increased intake of specific micronutrients could potentially improve some of
the disease symptoms, however special caution should be taken to avoid
over-supplementation and to avoid adverse effects such as hypercalciuria,
ectopic calcifications, GI-upset and nephrocalcinosis in case of calcium
over-supplementation.