This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rieger-Wettengl, G.
Right arrow Articles by Schoenau, E.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Rieger-Wettengl, G.
Right arrow Articles by Schoenau, E.
Related Collections
Right arrow Musculoskeletal System

PEDIATRICS Vol. 108 No. 6 December 2001, pp. e107


ELECTRONIC ARTICLE

Analysis of the Musculoskeletal System in Children and Adolescents Receiving Anticonvulsant Monotherapy With Valproic Acid or Carbamazepine

Gabriele Rieger-Wettengl, MD, Bärbel Tutlewski, RT, Angelika Stabrey, RT, Frank Rauch, MD, Peter Herkenrath, MD, Ulrike Schauseil-Zipf, MD and Eckhard Schoenau, MD

From the Children’s Hospital, University of Cologne, Cologne, Germany

Objective. To examine bone development in children and adolescents who have uncomplicated idiopathic epilepsy and had received monotherapy with carbamazepine or valproic acid for at least 1 year.

Methods. Thirty-nine patients from 6 to 19 years of age (18 girls) were studied. Total bone mineral content (BMC) and trabecular volumetric bone mineral density were measured at the distal radius using peripheral quantitative computed tomography. Maximum isometric grip force was determined with a standard dynamometer. Alkaline phosphatase activity and deoxypyridinoline (a marker of bone resorption) were assessed in serum and urine, respectively.

Results. Trabecular volumetric bone mineral density was significantly decreased in the entire group (z score mean ± standard deviation: -0.62 ± 1.04) and in the subgroup using valproic acid (-0.75 ± 1.18). In the carbamazepine subgroup, there was a similar but nonsignificant trend (-0.50 ± 0.90). Total BMC and isometric maximum grip force were normal in the entire study population (0.10 ± 1.22) and in the 2 subgroups. The relationship between BMC and grip force was similar between patients and healthy participants. Urinary levels of deoxypyridinoline were significantly elevated above normal in the whole study population (1.35 ± 2.00) and in both the valproic acid and the carbamazepine subgroups.

Conclusion. Bone turnover can be increased, but bone mass is adequate in children and adolescents who have uncomplicated idiopathic epilepsy and who receive monotherapy with carbamazepine or valproic acid.

Key Words: anticonvulsant • bone density • bone mass • bone metabolism • muscle

Abbreviations: CBZ, carbamazepine • VPA, valproic acid • BMD, bone mineral density • vBMD, volumetric bone mineral density • pQCT, peripheral quantitative computed tomography • BMC, bone mineral content • SD, standard deviation


Received for publication Apr 16, 2001; Accepted Jul 25, 2001.