The panel / Androgens
LH and FSH
If your testosterone is genuinely low, this is the test that decides what happens next. LH and FSH tell us whether the problem is in the testicles or in the brain that signals them. Those are different diseases with different treatments, and one of them is frequently reversible without any hormone at all.
What it measures
LH and FSH are the two signals your pituitary sends to your testicles. LH tells them to make testosterone. FSH drives sperm production. Your brain reads how much testosterone is circulating and adjusts both accordingly, so their level tells us whether the signal is being sent and ignored, or never sent at all.
This is a branch point, not a severity score. The number matters far less than which direction it moved relative to the testosterone.
One point worth flagging: biotin, sold widely as a hair and nail supplement, interferes with the immunoassays used for LH and FSH and can distort the result. It needs to stop at least three days before the draw. Men taking it for hair loss often do not think of it as a medication and do not mention it.
Why it is on the panel
Because low testosterone is a finding, not a diagnosis, and this is what turns one into the other. Without it you know a man is low but not why, and the why determines everything: whether to look for a pituitary tumour, whether the cause is a medication he could stop, whether weight loss would fix it, and whether starting testosterone would cost him his fertility permanently or temporarily.
Interpretation
Reading the result
The pattern is read against the testosterone, never alone. There are two that matter and they point in opposite directions.
In primary hypogonadism the FSH rise reflects damage to the sperm-producing tubules, and sperm production is usually hit harder than testosterone production. In secondary hypogonadism both fall together, because the single missing signal drives both.
What produces a secondary pattern without pituitary disease
This matters because the secondary pattern is common and frequently has a cause that is neither a tumour nor permanent.
What happens next
A primary pattern prompts consideration of karyotype testing, because Klinefelter syndrome is the most common cause and is frequently undiagnosed into adulthood.
A secondary pattern prompts prolactin, iron studies, a full medication review, and an assessment of the other pituitary hormones.
A secondary pattern in a man under 50, or with headaches, visual changes, very low gonadotropins or a testosterone below 150, prompts pituitary imaging.
If fertility matters, the branch decides the options. That conversation happens before any testosterone is prescribed, not after.