Elevated plasma concentrations of homocysteine in antiepileptic drug treatment

Citation
M. Schwaninger et al., Elevated plasma concentrations of homocysteine in antiepileptic drug treatment, EPILEPSIA, 40(3), 1999, pp. 345-350
Citations number
37
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EPILEPSIA
ISSN journal
00139580 → ACNP
Volume
40
Issue
3
Year of publication
1999
Pages
345 - 350
Database
ISI
SICI code
0013-9580(199903)40:3<345:EPCOHI>2.0.ZU;2-H
Abstract
Purpose: Homocysteine is an experimental convulsant and an established risk factor in artherosclerosis. A nutritional deficiency of vitamin B-6 vitami n B-12, or folate leads to increased homocysteine plasma concentrations. Du ring treatment with carbamazepine (CBZ), phenytoin, or phenobarbital, a def iciency in these vitamins is common. The objective of the study was to test the hypothesis that antiepileptic drug (AED) treatment is associated with increased homocysteine plasma concentrations. Methods. A total of 51 consecutive outpatients of our epilepsy clinic recei ving stable, individually adjusted AED treatment and 51 sex- and age-matche d controls were enrolled in the study. Concentrations of total homocysteine and vitamin B-6 were measured in plasma; vitamin B-12 and folate were meas ured in the serum of fasted subjects. Results: Patients and controls differed significantly in concentrations of folate (13.5 +/- 1.0 vs. 17.4 +/- 0.8 nM and vitamin B-6 (39.7 +/- 3.4 vs. 66.2 +/- 7.5 nnM), whereas serum concentrations of vitamin B-12 were simila r. The homocysteine plasma concentration was significantly increased to 14. 7 +/- 3.0 mu M in patients compared with controls (9.5 +/- 0.5 mu M; p < 0. 05, Wilcoxon rank-sum test). The number of patients with concentrations of >15 mu M was significantly higher in the patient group than among controls. The same result was obtained if only patients with CBZ monotherapy were in cluded. Patients with increased homocysteine plasma concentrations had lowe r folate concentrations. Conclusions: These data support the hypothesis that prolonged AED treatment may increase plasma concentrations of homocysteine, although the alternati ve explanation that increased homocysteine plasma concentrations are associ ated with the disease and not the treatment cannot be completely excluded a t the moment.