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Testosterone Deficiency
Overview
Testosterone production declines naturally with age. Testosterone
deficiency (TD) may result from disease or damage to the hypothalamus,
pituitary gland, or testicles that inhibits hormone secretion and
testosterone production, also known as hypogonadism. Depending on
age, insufficient testosterone production can lead to abnormalities in
muscle and bone development, underdeveloped genitalia, and diminished
virility.
Testosterone is the androgenic hormone primarily responsible for normal
growth and development of male sex and reproductive organs, including the
penis, testicles, scrotum, prostate, and seminal vesicles. It facilitates
the development of secondary male sex characteristics such as musculature,
bone mass, fat distribution, hair patterns, laryngeal enlargement, and vocal
chord thickening. Additionally, normal testosterone levels maintain energy
level, healthy mood, fertility, and sexual desire.
The testes produce testosterone regulated by a complex
chain of signals that begins in the brain. This chain is called the
hypothalamic-pituitary-gonadal axis. The hypothalamus secretes
gonadotropin-releasing hormone (GnRH) to the pituitary gland in carefully
timed pulses (bursts), which triggers the secretion of leutenizing hormone (LH)
from the pituitary gland. Leutenizing hormone stimulates the Leydig cells of
the testes to produce testosterone. Normally, the testes produce 4–7
milligrams (mg) of testosterone daily.
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here to complete the Androgen Deficiency in Aging Males (ADAM)
questionnaire.
Incidence and Prevalence
Testosterone production increases rapidly at the onset of puberty and
decreases rapidly after age 50 (to 20% to 50% of peak level by age 80).
Approximately 8 million men in the United States experience testosterone
deficiency; approximately 600,000 receive treatment.
Types and Causes
Hypogonadsim is classified by the location of its cause along the
hypothalamic-pituitary-gonadal axis:
- Primary, disruption in the testicles
- Secondary, disruption in the pituitary
- Tertiary, disruption in the hypothalamus
Disease, injury, surgery, and drug side effects can cause hypogonadism
and testosterone deficiency. Hypogonadism is congenital or
acquired, depending on the nature of the underlying condition.
Congenital causes include the following:
- Anorchia (vanishing testes syndrome; causing primary hypogonadism)
- Cryptorchidism (failure of testicles to descend into scrotum; causing
primary hypogonadism)
- Hormonal deficiency (e.g., deficiency of leutenizing hormone releasing
hormone; causing secondary or tertiary hypogonadism)
- Kallmann syndrome (insufficient hypothalamic GnRH production; causing
tertiary hypogonadism)
- Klinefelter syndrome (underdeveloped testicles; causing primary
hypogonadism
Acquired causes include the following:
- Chemotherapy
- Damage occurring during surgery involving the pituitary gland,
hypothalamus, or testes
- Glandular malformation
- Head trauma (affecting the hypothalamus)
- Infection (e.g., meningitis, syphilis, mumps)
- Isolated LH deficiency (e.g., fertile eunuch syndrome)
- Radiation
- Testicular trauma
- Tumors (of the pituitary gland, hypothalamus, or testicles)
Signs and Symptoms
Signs depend on the age of onset and the duration of hormonal deficiency.
Congenital hypogonadism is generally characterized by underdeveloped
genitalia (testes that do not descend into the scrotum) and, occasionally,
undeterminable genitalia. The development of hypogonadism near puberty
can result in gynecomastia (enlargement of breast tissue), sparse or absent
pubic and body hair, and underdeveloped penis, testes, and muscle. Adult
men may experience diminished libido, erectile dysfunction, muscle weakness,
loss of body hair, depression, and other mood disorders.
Complications Testosterone deficiency has been linked to muscle weakness and
osteoporosis. In one study, proximal and distal muscle weakness was
detected in 68% of men with primary or secondary hypogonadism. Spinal,
trabecular, and radial cortical bone density may also be significantly
reduced in testosterone-deficient men. Thirty percent of men with spinal
osteoporosis have long-standing testosterone deficiency, and one-third of
men have subnormal bone density that puts them at risk for fracture. |