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Zhonghua yi xue za zhi 2014-Dec

[Clinical efficacy of levetiracetam on bone mineral density and bone metabolism in middle-aged and elderly patients with generalized tonic-clonic seizures].

Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
L'enllaç es desa al porta-retalls
Xuejun Chen
Hui Wang

Paraules clau

Resum

OBJECTIVE

To explore the effects of levetiracetam (LEV) on the changes of bone mineral density (BMD) and bone metabolism in the treatment of middle-aged and elderly patients with generalized tonic-clonic seizures.

METHODS

A total of 112 patients with generalized tonic-clonic seizures from October 2012 to March 2014 were selected and divided into LEV and non-medication groups according to therapeutic methods (n = 56 each). LEV was administered to LEV group at an initial dosage of 500 mg twice daily. The same dose of LEV could be added every 2 or 3 weeks based on clonic seizure condition and tolerance. And the maximal dosage was 2 000 mg. The therapeutic duration was ≥ 6 months. No anti-seizure drug was offered for non-medication group. Another 50 healthy subjects served as control group. After 6-month treatment the clinical efficacy of LEV group was evaluated. BMD was detected with bone sonometer (DPX-L) and serum levels of blood calcium (Ca), blood phosphorus (P), alkaline phosphatase and parathyroid hormone were also detected in control group, pre-treatment in non-medication group and post-treatment in LEV group.

RESULTS

The rate of abnormal bone volume in non-medication (28.6%) and LEV groups (48.2%) were evidently higher than that in control group (4.0%) (P < 0.05). And it was apparently higher in LEV group than that in non-medication group (P < 0.05). BMD decreased obviously at post-treatment than pre-treatment (P < 0.05). And the post-treatment levels of Ca and P decreased markedly [(2.12 ± 0.19) vs (2.32 ± 0.23) mmol/L; (0.96 ± 0.01) vs (1.23 ± 0.12) mmol/L] while serum levels of alkaline phosphatase and parathyroid hormone increased significantly in LEV group than pre-treatment [(66 ± 6) vs (33 ± 3) µg/L; (62 ± 5) vs (34 ± 3) pmol/L, P < 0.05]. The clinical efficacy of LEV treatment at 1 month was similar to that at 6 months (both 98.21%). And the difference was insignificant (P > 0.05).

CONCLUSIONS

Single use of LEV is efficacious in the treatment of middle-aged and elderly patients with generalized tonic-clonic seizures. However, both disease and anti-seizure drugs have certain effects on BMD. And long-term application of LEV may lead to bone metabolism dysfunction to some extent.

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