» Articles » PMID: 7239516

Chromosomal Investigations in Epileptic Children During Long-term Therapy with Phenytoin or Primidone

Overview
Journal Hum Genet
Specialty Genetics
Date 1981 Jan 1
PMID 7239516
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

In epileptic children the long-term therapy with anticonvulsant drugs is absolutely necessary. However, anticonvulsant drugs have been suspected to be mutagenic and teratogenic. To investigate this problem metaphase chromosome observations were performed using short-time culture of peripheral blood lymphocytes from twenty children. Ten of the children had been treated with phenytoin and the other ten with primidone on monotherapy. The long-term administration of anticonvulsant drugs was monitored by measurement of the serum concentrations of phenytoin and primidone, by seizure anamnesis, and by repeated EEG investigations. Analyzing 100 mitoses from each proband, we found no increase of structural or numerical aberrations in our patients compared with six controls. In adults, however, anticonvulsant drugs have been found to cause structural aberrations and chromosomal damage. The absence of these lesions in children may reflect the higher efficiency of DNA-repair in local DNA-damage.

Citing Articles

Chromosome fragile sites in mentally retarded males: increased incidence with seizures and diphenylhydantoin therapy.

Hodges K, Larson R, Butler M Ann Clin Lab Sci. 1998; 28(5):293-9.

PMID: 9784831 PMC: 5292046.


Increased sister chromatid exchanges in epileptic children during long-term therapy with phenytoin.

Habedank M, Esser K, Brull D, Kotlarek F, Stumpf C Hum Genet. 1982; 61(1):71-2.

PMID: 6813241 DOI: 10.1007/BF00291338.


Increased chromosomal breakage in epileptic children after long-term treatment.

Curatolo P, Brinchi V, Cusmai R, VIGNETTI P, Benedetti P Eur J Pediatr. 1986; 145(5):439-42.

PMID: 3098567 DOI: 10.1007/BF00439256.

References
1.
Ayraud N, KERMAREC J, MARTINON J . [Cytogenetic effects of anticonvulsants. Apropos of an observation of abnormalities transmitted during intra-uterine life]. Ann Genet. 1968; 11(4):253-7. View

2.
Littlefield L, GOH K . Cytogenetic studies in control men and women. I. Variations in aberration frequencies in 29,709 metaphases from 305 cultures obtained over a three-year period. Cytogenet Cell Genet. 1973; 12(1):17-34. DOI: 10.1159/000130434. View

3.
Kotlarek F, Faust J . Chromosomal investigations in children with pyknolepsy on dipropylacetate monotherapy. Hum Genet. 1978; 43(3):329-31. DOI: 10.1007/BF00278841. View

4.
Niedermuller H, Hofecker G, Kment A . [Gerontological investigations of the nucleic acid metabolism in the rat. II. DNA repair capacity in different ages (authors transl)]. Aktuelle Gerontol. 1978; 8(5):253-60. View

5.
Dudin G, Beek B, Obe G . The human leukocyte test system. I. DNA synthesis and mitoses in PHA-stimulated 2-day cultures. Mutat Res. 1974; 23(2):279-81. View