This clinical measure quantifies the portion of circulating testosterone that is not tightly bound to Sex Hormone-Binding Globulin (SHBG) and is therefore readily accessible to target tissues. It includes both free testosterone and the fraction loosely bound to albumin. The bioavailable status provides a more accurate reflection of the androgenic effect at the cellular level than total testosterone alone, especially in cases of altered SHBG levels. Clinically, this parameter is critical for assessing true hormonal deficiency and monitoring the efficacy of androgen optimization therapies.
Origin
The concept emerged from the recognition that total hormone concentration is an incomplete measure of biological activity, as plasma proteins bind a significant portion of steroid hormones. The term bioavailable was introduced to distinguish the fraction capable of traversing capillary membranes and interacting with receptors. This refinement in endocrinology allows for a more nuanced and physiologically relevant assessment of androgen status, particularly when evaluating symptoms of hypogonadism.
Mechanism
Testosterone is synthesized and released into the circulation where it binds primarily to SHBG and, to a lesser extent, to albumin. The high affinity of SHBG binding renders that fraction largely inert for immediate cellular uptake. Only the unbound (free) and albumin-bound testosterone can easily dissociate from their carriers to pass through the capillary wall and interact with androgen receptors inside target cells. The bioavailable status directly reflects this functional pool, driving anabolic and sexual function.
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