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J Clin Endocrinol Metab ; 88(12): 5778-83, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14671168

RESUMEN

Van Buchem disease is an autosomal recessive disease characterized by overgrowth of the skeleton. In a group of Dutch patients the disease is thought to be due to a 52-kb deletion that results in decreased expression of the SOST gene. To further characterize the disease, the morphology of the metacarpals of six adult subjects and two juveniles with Van Buchem disease were measured on hand x-rays along with nine normal adults and nine adult carriers of the disease. Serum bone formation markers, alkaline phosphatase, type I procollagen peptide, and osteocalcin, and the urinary bone resorption marker, cross-linked N-telopeptide, were determined. Van Buchem patients had increased metacarpal outer diameter, inner diameter, cortical thickness, and bone mineral density. Calculated bone volume and derived polar moment of inertia were markedly elevated (elevations of 158 +/- 33% and 497 +/- 95%, respectively) consistent with increased bone strength. Serum procollagen peptide and osteocalcin were significantly higher in Van Buchem patients. Urinary cross-linked N-telopeptide was significantly elevated in Van Buchem patients. None of these changes was found in Van Buchem carriers. These observations indicate that decreased expression of the SOST gene can lead to increased bone formation and to stronger bones.


Asunto(s)
Densidad Ósea , Hiperostosis Cortical Congénita/genética , Hiperostosis Cortical Congénita/fisiopatología , Osteogénesis , Adolescente , Adulto , Anciano , Biomarcadores/sangre , Biomarcadores/orina , Resorción Ósea/metabolismo , Estudios de Casos y Controles , Niño , Colágeno/orina , Colágeno Tipo I , Femenino , Genes Recesivos , Mano/diagnóstico por imagen , Heterocigoto , Humanos , Hiperostosis Cortical Congénita/diagnóstico por imagen , Masculino , Metacarpo/diagnóstico por imagen , Persona de Mediana Edad , Péptidos/orina , Radiografía
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