Carbamazepine and risk of hypothyroidism: a prospective study
Language English Country Denmark Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17850408
DOI
10.1111/j.1600-0404.2007.00883.x
PII: ANE883
Knihovny.cz E-resources
- MeSH
- Anticonvulsants adverse effects MeSH
- Diabetic Neuropathies drug therapy MeSH
- Adult MeSH
- Down-Regulation drug effects physiology MeSH
- Epilepsy drug therapy MeSH
- Hypothyroidism blood chemically induced physiopathology MeSH
- Carbamazepine adverse effects MeSH
- Middle Aged MeSH
- Humans MeSH
- Metabolic Clearance Rate drug effects physiology MeSH
- Monitoring, Physiologic standards MeSH
- Trigeminal Neuralgia drug therapy MeSH
- Prospective Studies MeSH
- Risk Factors MeSH
- Thyroid Gland drug effects metabolism physiopathology MeSH
- Thyrotropin blood MeSH
- Thyroxine blood pharmacology therapeutic use MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anticonvulsants MeSH
- Carbamazepine MeSH
- Thyrotropin MeSH
- Thyroxine MeSH
OBJECTIVES - While carbamazepine (CBZ) decreases thyroid hormone concentrations it rarely causes hypothyroidism. We assessed prospectively the early effect of CBZ on thyroid status in thyroxine-supplemented hypothyroid patients, when compared with patients without a thyroid disorder. METHODS - In 29 patients, thyrotropin (TSH), total thyroxine (TT4) and free thyroxine (FT4) serum levels were assayed before starting CBZ, and then weekly for 7 weeks. Nineteen patients with no thyroid disorder (group A) were compared with 10 thyroxine-supplemented hypothyroid patients, stable before CBZ treatment (group B). RESULTS - In group A, TT4 decreased significantly by ca. 15-25%, starting from the first week (Friedman, P < 0.001). FT4 decline was smaller (ca. 10-15%) and delayed till the second week. FT4/TT4 ratio increased significantly (P < 0.001), while TSH only slightly (P = 0.073), never exceeding normal range. In group B, similar TT4 and FT4 decline was followed by significantly increasing TSH (P = 0.011), while the FT4/TT4 ratio was not significantly changed. In 3 of 10 patients TSH rose over 5 mIU/l, necessitating treatment adjustment. CONCLUSIONS - In patients with no thyroid disorder, CBZ causes hormonal changes of no clinical relevance, due to adaptive response. In T4-supplemented hypothyroid patients this adaptation is lacking, CBZ may precipitate subclinical or overt hypothyroidism, and early thyroid function monitoring seems advisable.
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