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Hyposexuality and epilepsy: a community survey of hormonal and behavioural changes in male epileptics

Published online by Cambridge University Press:  09 July 2009

B. K. Toone*
Affiliation:
Department of Psychological Medicine, King's College Hospital, London
J. Edeh
Affiliation:
Department of Psychological Medicine, King's College Hospital, London
M. N. Nanjee
Affiliation:
Department of Psychological Medicine, King's College Hospital, London
M. Wheeler
Affiliation:
Department of Psychological Medicine, King's College Hospital, London
*
1Address, for correspondence: Dr B. K. Toone, Department of Psychological Medicine, King's College Hospital, Denmark Hill, London SE5 9RS.

Synopsis

A survey of five group practices in South London identified 60 male patients currently undergoing treatment for epilepsy. Fifty-four agreed to participate in a detailed enquiry into aspects of their sexual activity and behaviour. Anterior pituitary and sex-hormone levels were measured. The epileptic patients were characterized by low levels of sexual activity and interest. Temporal-lobe and non-temporal-lobe epileptics were indistinguishable in these respects, but when the latter group was further subdivided into primary generalized epilepsy and focal non-temporal lobe epilepsy, the focal groups (both temporal lobe and non-temporal lobe) were more impaired. Hormonal analysis confirmed earlier hospital-clinic-based reports. In the epilepsy group, plasma free testosterone and percentage free testosterone values were decreased, sex hormone binding globulin, luteinizing hormone (LH) and follicle stimulating hormone (FSH) were increased compared to values in a normal healthy population. As association between the behavioural and hormonal indices of hyposexuality was shown, particularly for LH, but this was less apparent than in previous work.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1989

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References

Barragry, J M., Makin, H L J., Trafford, D. J. H & Scott, D. F. (1978). Effect of anticonvulsants on plasma testosterone and sex hormone binding globulin levels. Journal of Neurology, Neurosurgery and Psychiatry 412, 913914.CrossRefGoogle Scholar
Blumer, D. & Walker, A. E. (1967). Sexual behaviour in temporal lobe epilepsy Archives of Neurology 16, 3743.CrossRefGoogle ScholarPubMed
Christiansen, P., Deigaard, J. & Lund, M. (1975). Potens, Fertilitet og Konshormonudskillelse hos Yngre Manglige Epilepsilidende. Ugeskrift für Laeger 137, 24022405.Google Scholar
Connell, W. G., Rapeport, G. H., Beastall, E. H. & BrodieN. J,. N. J,. (1984). Changes in circulating androgens during short term carbamazepine therapy. British Journal of Clinical Pharmacology 17, 347351.CrossRefGoogle ScholarPubMed
Dana-Haeri, J. & Richens, A. (1981). Effects of anti-epileptic drugs on the hypothalamic pituitary axis in epileptic patients. In Advances in Epileptology: XIIth Epilepsy International Symposium (ed. Dam, M., Gram, L. and Penry, J. K.), pp. 469475. Raven Press: New York.Google Scholar
Dana-Haeri, J., Oxley, J & Richens, A. (1982). Reduction of free testosterone by antiepileptic drugs. British Medical Journal 284, 8586CrossRefGoogle ScholarPubMed
Dana-Haeri, J., Oxley, J. & Richens, A. (1984). Pituitary responsiveness to gonadotrophin-releasing and thyrotrophin-releasing hormones in epileptic patients receiving carbamazepine or phenytoin. Clinical Endocrinology 20, 163168.CrossRefGoogle ScholarPubMed
Dansky, L., Andermann, E. & Andermann, F (1980). Marriage and fertility in epileptic patients. Epilepsia 21, 261271.CrossRefGoogle ScholarPubMed
Driver, M. V. (1970). Electroencephalogram and the diagnosis of temporal lobe disease. In Modern Trends in Psychological Medicine, Vol. 2 (ed, Price, J. H.), pp. 326345. Butterworths: London.Google Scholar
Ervin, F. R. (1967). Brain disorders associated with convulsions. In Comprehensive Textbook of Psychiatry (ed, Freedman, A. M. and Kaplan, H. I.), pp. 11381157. Williams and Wilkins: Baltimore.Google Scholar
Fenwick, P. B. C., Toone, B. K., Wheeler, M.Nanfec, M., Grant, R. & Brown, D. (1985). Sexual behaviour in a centre for epilepsy Acta Neurologica Scandinavica 17, 428435.Google Scholar
Gastaut, H. & Collomb, H. (1954). Etude du comportement sexual chez les epileptiques psychomoteurs. Annales Medico-Psychologiques 112, 657696.Google Scholar
Gunn, J. & Fenton, G. W. (1969). Epilepsy in prisons: a diagnostic survey. British Medical Journal iv, 326328.CrossRefGoogle Scholar
Hoffman, H. & Kahlert, T. (1981). The effects of prolonged anticonvulsant treatment on the sexual hormone of male epileptic patients. Nervanarzt 52, 715717.Google Scholar
Krafft-Ebing, R. (1931). Psychopathia Sexualis Physicians and Surgeons Book Co., New York.Google Scholar
Lindsay, J., Ounsted, C. & Richards, P. (1979). Long-term outcome in children with temporal lobe seizures. II. Marriage, parenthood and sexual indifference. Developmental Medicine and Child Neurology 21, 433440.CrossRefGoogle ScholarPubMed
Luhdorf, K, Christiansen, P., Hansen, J. M. & Lund, M. (1977). The influence of phenytoin and carbamazepine on endocrine function. preliminary results. In Epilepsy, the VIIIth International Symposium (ed Penry, J. K.), pp. 209213. Raven Press: New YorkGoogle Scholar
Pritchard, P. D. (1980). Hyposexuality: a complication of complex partial epilepsy. Transactions of the American Association 105, 193195.Google Scholar
Puri, V. & Puri, C. P. & Anandkumar, T. C. (1981) Serum levels of dihydrotestosterone in male rhesus monkeys estimated by a nonchromotographic radioimmuno-assay method. Journal of Steroid Biochemistry 14, 877881.CrossRefGoogle Scholar
Reynolds, E. H., Lewes, R. D C & Shorvon, S. D. (1983). Why does epilepsy become intractable? Prevention of chronic epilepsy. Lancet ii, 952954.CrossRefGoogle Scholar
Rosner, W. (1972) A simplified method for the quantitative determination of testosterone-estradiol-binding globulin activity in human plasma. Journal of Clinical Endocrinology and Metabolism 34, 983988.CrossRefGoogle ScholarPubMed
Saunders, M. & Rawson, M (1970). Sexuality in male epileptics. Journal of the Neurological Sciences 10, 577583.CrossRefGoogle ScholarPubMed
Shukla, G. D, Srivastave, O. N. & Katiyar, B C. (1979). Sexual disturbances in temporal lobe epilepsy a controlled study. British Journal of Psychiatry 134, 288292.CrossRefGoogle ScholarPubMed
Taylor, D C (1969). Sexual behaviour and temporal lobe epilepsy Archives of Neurology 21, 510516.CrossRefGoogle ScholarPubMed
Toone, B. K. (1986). Sexual disorders in epilepsy. In Recent Advances in Epilepsy, 3, (ed Pedley, T A. and Meldrum, B. S), pp 233259. Churchill Livingstone: EdinburghGoogle Scholar
Toone, B K., Wheeler, M & Fenwick, P. B. C. (1980). Sex hormone changes in male epileptic patients. Clinical Endocrinology 12, 391395.CrossRefGoogle Scholar
Toone, B K., Wheeler, M., Nanjee, M., Fenwick, P. B. C. & Grant, R. (1983). Sex hormones, sexual drive and plasma anticonvulsant levels in male epileptics. Journal of Neurology, Neurosurgery and Psychiatry 46, 824826CrossRefGoogle Scholar
Toone, B. K., Edeh, J, Fenwick, P. B C, Grant, R., Nanfec, N.Purches, A. C. & Wheeler, M (1985). Hormonal and behavioural changes in male epileptics. In Advances in Epileptology XVth Epileptology International Symposium (ed, Porter, R. J., Mattson, R. H., Ward, A. A. and Dam, M), pp 283290Raven Press New York.Google Scholar
Wheeler, M J. & Luther, F. (1983). Development of testosterone radio-immunoassays for routine use In Immunoassays for Clinical Chemistry (ed Hunter, W M and Corrie, J. E. T.), pp. 113116. Churchill Livingstone Edinburgh.Google Scholar
Wheeler, M. J. & Nanjee, M. N. (1985). A steady-state gel filtration method on micro-columns for the measure of percentage free testosterone in serum. Annals of Clinical Biochemistry 22, 195–189.CrossRefGoogle ScholarPubMed