This refers to the precise laboratory measurement of the fraction of testosterone in the bloodstream that is not tightly bound to Sex Hormone-Binding Globulin (SHBG) and is therefore readily available to target tissues. This fraction includes both Free Testosterone and Albumin-bound Testosterone, which can easily dissociate to interact with androgen receptors. Clinically, this quantification is a superior indicator of androgenic activity compared to Total Testosterone alone, offering a more accurate assessment of a patient’s functional hormonal status. Accurate measurement is crucial for diagnosing androgen deficiency and monitoring therapeutic effectiveness.
Origin
The concept originated in clinical endocrinology, arising from the recognition that Total Testosterone levels often do not correlate perfectly with clinical symptoms due to variations in SHBG concentration. The term ‘Bioavailable’ was introduced to delineate the portion of the hormone that is biologically active. Quantification methods, such as equilibrium dialysis or calculated indices, were developed to provide a more functional metric for patient care.
Mechanism
Testosterone circulates in three forms: tightly bound to SHBG, loosely bound to albumin, and unbound (free). SHBG binds testosterone with high affinity, effectively sequestering it and preventing immediate biological action. Albumin binding is weaker, allowing the hormone to dissociate and enter cells, classifying it as bioavailable. Quantification relies on methods that separate or calculate the concentrations of these different fractions to reflect the true level of active hormone.
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