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January 1, 1974Clinical Endocrinology1,137 citations

Sex‐hormone‐binding Globulin

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DADavid C. Anderson

Key Points

  • To review the mechanisms by which plasma sex-hormone-binding globulin modulates sex-steroid hormone action in target tissues and assess its clinical relevance in endocrine diseases.
  • Synthesized physiological and clinical evidence on steroid hormone binding to plasma transport proteins.
  • Assessed the reciprocal interactions between sex-hormone-binding globulin levels, androgen and estrogen balance, and thyroid hormone regulation.
  • Determined that only unbound steroid hormones penetrate cells, with elevated sex-hormone-binding globulin decreasing testosterone activity and increasing estrogen production.
  • Showed that elevated androgen levels inhibit sex-hormone-binding globulin production, amplifying androgen action and contributing to disorders like hirsutism and gynaecomastia.
  • Highlighted that monitoring sex-hormone-binding globulin levels serves as an effective diagnostic tool to evaluate therapeutic responses to glucocorticoid and estrogen treatments.

Abstract

A review was made to understand how plasma binding protein might influence sex-hormone action in target tissues. Steroids are predominately bound to plasma proteins and only unbound steroids enter the cells. Sex-hormone-binding globulin (SHBG) binds to both the main circulating steroid T and E2 but changes in SHBG concentrations exert significant results. Increased SHBG levels increase estrogen production and decreases T activity; whereas, increased androgens increase T action and inhibit SHBG production. These disturbances in hormone maintenance may lead to abnormal adult sex differentiation such as hirsutism and forms of hynaecomastia. By developing SHBG concentration measurement methods-responses of hirsutism to glucocorticoid or estrogem may be assessed. In addition, the effect of thyroid hormones on SHBG may also have therapeutic implications in endocrine disease.

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Cite This Study

David C. Anderson (1974) studied this question.

synapsesocial.com/papers/6a10bf2c8102eb4b66ee4dd9https://doi.org/10.1111/j.1365-2265.1974.tb03298.x
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