Hypoandrogenism cognitive impact describes the measurable deficits in specific cognitive domains that result from abnormally low levels of androgen hormones, such as testosterone and dehydroepiandrosterone (DHEA), in both men and women. The most common manifestations include reductions in verbal memory, processing speed, and executive function, often reported as “brain fog” or difficulty concentrating. This impact is a significant clinical concern, particularly in aging populations and in patients undergoing hormone-suppressing therapies.
Origin
The term combines hypo- (low), androgenism (androgen levels), and cognitive impact, reflecting a clear cause-and-effect relationship established through decades of neuroendocrinology research. Early studies focused on male hypogonadism, but more recent research highlights the sex-specific, yet equally critical, role of androgens in female brain health, often interacting with genetic risk factors like the APOE-ε4 allele.
Mechanism
Androgens exert their cognitive effects through multiple neuroprotective mechanisms. Testosterone can be converted into estradiol via the aromatase enzyme, allowing it to act through both androgen and estrogen receptors widely distributed in the hippocampus and cortex. These hormones promote neuronal survival, enhance synaptic plasticity, and possess anti-inflammatory and antioxidant properties that directly protect nerve cells from age-related damage and stress-induced decline.
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