Biochemical Basis for the Selection of Oral Contraceptives
Abstract
Many specific plasma proteins show dose-related changes when oral estrogens are administered. Large increases in concentration are seen in many important binding proteins, such as the sex hormone-binding globulin, transcortin, the retinol-binding protein, ceruloplasmin, and transferrin. A smaller group of plasma proteins are reduced in amount. These changes are related to altered rates of hepatic synthesis and secretion. As the overall effect of estrogen is one of increased protein synthesis, there is a reduction in the amount of plasma-free amino acids and in the pattern of distribution. Oral contraceptive (OC) users frequently show significant alterations in biochemical tests of vitamin status, at least some of which are related to alterations in plasma proteins. Other biochemical changes associated with OC use include a fasting hyperlipidemia, due mainly to increases in triglycerides, although there is often also a small increase in cholesterol. These changes are due primarily to increases in several lipoprotein fractions and are related mainly to the estrogen component. A deterioration in glucose tolerance occurs in many OC users and is probably induced by both estrogens and progestogens. There is evidence that certain clinical side effects of OCs, such as depression, are associated with specific biochemical changes.
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Estrogen-containing products, like combined oral contraceptives but not their progesterone-only counterparts, are associated with an increase in SHBG concentration and other major changes in several plasma protein profiles.
“Among others, estrogen-containing products, like combined oral contraceptives (COC) but not their progesterone-only counterparts, are associated with an increase in SHBG concentration and other major changes in several plasma protein profiles [100].”
From Role of sex hormone-binding globulin in the free hormone hypothesis and the relevance of free testosterone in androgen physiology (2022) · cites this paper as [100]
Cites
Mechanism of hypertriglyceridaemia associated with contraceptive steroids.
Kissebah, A., Harrigan, P., & Wynn, V. (1973) · Hormone and Metabolic Research · doi:10.1055/s-0028-1093969 · Cited by 106 · see citing works
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Narinx, N., David, K., Walravens, J., Vermeersch, P., Claessens, F., Fiers, T., Lapauw, B., Antonio, L., & Vanderschueren, D. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04562-1 · Cited by 96 · see citing works
- Authors
- Briggs, M. H.
- Affiliations
- Deakin University (AU)
- Corresponding author
- Briggs, Michael H.
- Venue
- International Journal of Gynecology & Obstetrics
- Publisher
- Wiley
- Published
- 1979-11
- Volume
- 16
- Issue
- 6
- Pages
- 509-517
- ISSN
- 0020-6695 (ISSN-L)
- 0020-7292
- OpenAlex
- W2409098827
- Cited by
- 26
- References
- 1
- Citations by year
- 2025: 1 · 2024: 1 · 2022: 2 · 2015: 1
- FWCI
- 1.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- International Journal of Gynecology & Obstetrics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Reproductive Health and Contraception
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Interaction Studies and Fluorescence Analysis
- Keywords
- oral contraceptives, estrogen, progestogens, sex hormone-binding globulin, corticosteroid-binding globulin, retinol-binding protein, ceruloplasmin, transferrin, plasma protein binding, hepatic protein synthesis, vitamin status, triglycerides, lipoproteins, glucose tolerance, depression, contraceptive side effects
- MeSH terms
- Amino Acids, Blood Proteins, Cholesterol, Contraceptives, Oral, Contraceptives, Oral, Synthetic, Erythrocytes, Female, Fibrinogen, Humans, Insulin, Lipoproteins, Pregnancy, Proteins, Serum Albumin, Triglycerides, Vitamins, Carbohydrate Metabolism, Lipid Metabolism
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