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EVALUATION OF BONE ATROPHY BY MICRODENSITOMETORY AND EFFECT OF ACTIVE VITAMIN D3 (la-OH-D3) ADMINISTRATION IN PATIENTS RECEIVING ANTICONVULSANTS Yoshiaki Takeno 1 1Department of Neurosurgery, Fukuoka Red Cross Hospital pp.887-893
Published Date 1989/9/1
DOI https://doi.org/10.11477/mf.1406206385
  • Abstract
  • Look Inside

Attention has been paid to bone atrophy caused by oral anticonvulsants.

Bone atrophy has been judged on X-ray picture in combination with measuring bio-chemical para-meters such as serum caclium (Ca), phosphorus (P) and alkaline phosphatase (Alp), and assessing X-ray findings such as bone density and morpho-logical findings of bone. However, the conventional techniques based on these parameters and findings do not always permit diagnosing the disease. Microdensitometric (MD) method, recently de-veloped by Inoue et al.39) as a method to assess the grades of severity of bone atrophy on X-ray picture of the metacarpal bone II, has been improved in its exactitude and widely applied in clinical practice for diagnosis of bone atrophy. In 174 patients receiving anticonvulsants, the severityof bone atrophy was quantitatively assesed by the MD method. 1 、μg/day of active vitamin D3 (1α-OH-D3) was administered to patients pre-senting abnormal MD findings indicative of bone atrophy, and the results were as follows :

1. Bone atrophy of grades initial to III was noted in 46 patients (26. 4%). There was no sex-difference in incidence of bone atrophy.

2. In patients receiving valproic acid (VPA) for two years or longer, there was no correlation between the duration of VPA treatment and the severity of the disease as assessed by MD method or its incidence, nor between the mean blood level of VPA and the severity.

3. Bone atrophy was found in 25 (29.1%) of the patients receiving anticonvulsants even for less then two years. Five of these 25 patients were alcoholists, and 9 patients received steroids. There were three women aged over 60 years.

4. Forty four patients (28 males and 21 females) were treated with 1α-OH-D3. MD parameters turn-ed to normal in 7 patients and 4 patients 6 months and one year after the initiation of treatment with the drug, respectively.

5. MD parameters all trended to decrease in la-OH-D3 non-treated group, while they increased in 1 a-OH-D3 treated group, indicating that the drug was effective, at least, to prevent the loss of bone mineral. Hypercalcemia, the most common side effect of the drug, was not found in any pa-tients.

In conclusion, 1 μg/day of 1 a-OH-D3 was assess-ed to be useful for improvement of bone disease in anticonvulsant-receiving patients.


Copyright © 1989, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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