Effects of oral contraceptives on thyroid function and vice versa.
Blood Coagulation
/ drug effects
Cardiovascular Diseases
/ epidemiology
Contraception
/ methods
Contraceptives, Oral
/ pharmacology
Drug Interactions
Female
Fertility
/ drug effects
Hormone Replacement Therapy
Humans
Risk Factors
Thyroid Diseases
/ epidemiology
Thyroid Gland
/ drug effects
Thyroxine
/ pharmacology
Triiodothyronine
/ physiology
Hormonal contraception
Hypothalamic
Pituitary
TBG
Thyroid axis
Journal
Journal of endocrinological investigation
ISSN: 1720-8386
Titre abrégé: J Endocrinol Invest
Pays: Italy
ID NLM: 7806594
Informations de publication
Date de publication:
Sep 2020
Sep 2020
Historique:
received:
02
01
2020
accepted:
17
03
2020
pubmed:
29
3
2020
medline:
3
6
2021
entrez:
29
3
2020
Statut:
ppublish
Résumé
Thyroid gland dysfunction represents an epidemiologically relevant disease in the female gender, where treatment with oral contraceptives (OCs) is frequently prescribed. Although OCs are able to impact the thyroid gland function, scanty data have been released on this matter so far. The aim of this article was to review how hormonal OCs, including estrogen- or progesterone-only containing medications, interact with the hepatic production of thyroid-binding globulin (TBG) and, consequently, their effects on serum levels of thyroxine (T4) and triiodothyronine (T3). We also reviewed the effect of Levo-T4 (LT4) administration in women taking OCs and how they influence the thyroid function in both euthyroid women and in those receiving LT4. The estrogenic component of the pills is capable of increasing various liver proteins, such as TBG, sex hormone-binding protein (SHBG) and coagulation factors. On the other hand, the role of progestogens is to modulate estrogen-dependent effects mainly through their anti-androgenic action. In fact, a reduction in the effects of androgens is useful to keep the thromboembolic and cardiovascular risks low, whereas OCs increase it especially in women with subclinical hypothyroidism or in those treated with LT4. Accordingly, subclinical hypothyroidism is known to be associated with a higher mean platelet volume than normal and this increases cardiovascular risk due to platelet hyperactivity caused by incomplete thrombocytopoietic maturation.
Sections du résumé
BACKGROUND
BACKGROUND
Thyroid gland dysfunction represents an epidemiologically relevant disease in the female gender, where treatment with oral contraceptives (OCs) is frequently prescribed. Although OCs are able to impact the thyroid gland function, scanty data have been released on this matter so far.
AIM
OBJECTIVE
The aim of this article was to review how hormonal OCs, including estrogen- or progesterone-only containing medications, interact with the hepatic production of thyroid-binding globulin (TBG) and, consequently, their effects on serum levels of thyroxine (T4) and triiodothyronine (T3). We also reviewed the effect of Levo-T4 (LT4) administration in women taking OCs and how they influence the thyroid function in both euthyroid women and in those receiving LT4.
REVIEW
METHODS
The estrogenic component of the pills is capable of increasing various liver proteins, such as TBG, sex hormone-binding protein (SHBG) and coagulation factors. On the other hand, the role of progestogens is to modulate estrogen-dependent effects mainly through their anti-androgenic action. In fact, a reduction in the effects of androgens is useful to keep the thromboembolic and cardiovascular risks low, whereas OCs increase it especially in women with subclinical hypothyroidism or in those treated with LT4. Accordingly, subclinical hypothyroidism is known to be associated with a higher mean platelet volume than normal and this increases cardiovascular risk due to platelet hyperactivity caused by incomplete thrombocytopoietic maturation.
Identifiants
pubmed: 32219692
doi: 10.1007/s40618-020-01230-8
pii: 10.1007/s40618-020-01230-8
doi:
Substances chimiques
Contraceptives, Oral
0
Triiodothyronine
06LU7C9H1V
Thyroxine
Q51BO43MG4
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM