Cited by 166Pharmacological Effects and Toxicity StudiesEpilepsy research and treatmentThyroid Disorders and Treatments

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Serum Hormones in Male Epileptic Patients Receiving Anticonvulsant Medication

Isojarvi, J. I. T., Pakarinen, A. J., Ylipalosaari, P. J., Myllyla, V. V.·1990·Archives of Neurology

Abstract

Circulating sex and thyroid hormones, as well as the pituitary function, were assessed in 63 male patients with epilepsy receiving either a single medication of carbamazepine, phenytoin, or valproate or a combination of carbamazepine plus phenytoin or carbamazepine plus valproate. All therapeutic regimens, including carbamazepine and/or phenytoin were associated with low levels of circulating thyroxine (T4), free thyroxine (FT4), and dehydroepiandrosterone sulfate, and with low values for the free androgen index, and phenytoin and carbamazepine plus phenytoin were associated with high serum concentrations of sex hormone-binding globulin. These hormone parameters were unaffected by valproate monotherapy. It seems probable that accelerated hormone metabolism is responsible for the hormonal changes found in patients treated with carbamazepine and/or phenytoin. However, every drug regimen studied also had depressant and/or stimulatory effects on the function of the hypothalamic-pituitary axis. The diverse endocrine effects of different antiepileptic drug regimens should be considered when starting antiepileptic drug therapy.

Overview

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Registry

Crossref · 10.1001/archneur.1990.00530060082023

Cites

1 of 1 references verified0 citation errors · 0 not checkable

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  • Administration of some antiepileptic drugs (phenobarbital, phenytoin, carbamazepine) can induce hepatic microsomal enzymes, resulting in an increase of SHBG concentration that lowers T bioavailability.

    “Administration of some antiepileptic drugs (e.g., phenobarbital, phenytoin and carbamazepine) can induce hepatic microsomal enzymes. This results in an increase of SHBG concentration that in turn influences free circulating androgen levels, lowering T bioavailability [107–109].”

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Metadata

Authors
Isojarvi, J. I. T., Pakarinen, A. J., Ylipalosaari, P. J., & Myllyla, V. V.
Venue
Archives of Neurology
Published
1990-06-01
Volume
47
Issue
6
Pages
670-676
ISSN
0003-9942 (ISSN-L)
OpenAlex
W2148667829
Cited by
166
References
1
Citations by year
2026: 2 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 3 · 2020: 2 · 2018: 4 · 2017: 1 · 2016: 4 · 2015: 5 · 2014: 1 · 2013: 3 · 2012: 5
FWCI
6.99
Type
journal article
Language
en
Open access
closed
Locations
  • Archives of Neurology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmacological Effects and Toxicity Studies
  • Health Sciences › Medicine › Clinical Neurology › Epilepsy research and treatment
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
Keywords
epilepsy, antiepileptic drugs, sex hormones, thyroid hormones, thyroxine, dehydroepiandrosterone sulfate, free androgen index, sex hormone-binding globulin, hypothalamic-pituitary axis, carbamazepine, phenytoin, valproic acid, male patients
MeSH terms
Adolescent, Adult, Anticonvulsants, Epilepsy, Follicle Stimulating Hormone, Humans, Luteinizing Hormone, Male, Middle Aged, Gonadal Steroid Hormones, Thyroid Hormones

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