Progesterone (Post-menopausal)

Optimal result: 0 – 0.22 ng/mg Creat/Day

In cycling females, progesterone is primarily produced in the corpus luteum of the ovaries, and to a lesser degree in the adrenal glands. Menopausal females continue to produce small amounts of progesterone in the adrenal glands. Elevated levels of progesterone may be due to high dose pregnenolone supplementation, progesterone supplementation, exogenous progesterone exposure, pregnancy, disorders of luteinization, increased HSD3A activity, reduced activity of CYP21A or CYP17A, and rarely thecal cell tumors. In addition, elevations of both progesterone and pregnanediol, progesterone’s major metabolite, have been reported in 21-hydroxylase deficiency.

In cycling females, progesterone is produced in the corpus luteum of the ovaries, and to a lesser extent the adrenal glands. Menopausal females continue to produce small amounts of progesterone in the adrenal glands. Low/low range levels of progesterone may be due to anovulation, amenorrhea, perimenopause and menopause.

Progesterone is produced by the corpus luteum following ovulation and to a lesser extent by the adrenal glands in both sexes. While found in the urine in small amounts, progesterone can be seen as a clinical marker of luteul activity and theraputic oral progesterone administration. The most important progesterone metabolite, pregnanediol (PDL), can serve as a urinary marker for endogenous progesterone levels and as an indicator of ovulation.

Progesterone is produced by the corpus luteum following ovulation and to a lesser extent by the adrenal glands in both sexes. While found in the urine in small amounts, progesterone can be seen as a clinical marker of luteul activity and theraputic oral progesterone administration. The most important progesterone metabolite, pregnanediol (PDL), can serve as a urinary marker for endogenous progesterone levels and as an indicator of ovulation.

PDL exists as two isomers, 5α-pregnanediol and 5β-pregnanediol.

5β-pregnanediol represents the majority end point of endogenous progesterone metabolism and appears to have little activity within the body, while 5α-pregnanediol, the lesser metabolite of PDL, can cross the blood brain barrier and may partially agonize GABA-A receptors. This action is possibly due to its role as an immediate precursor to allopregnanolone. Allopregnanolone is a potent neuroactive steroid capable of binding the GABA-A receptor often leading to sedative and anxiolytic action. The calming action of allopregnanolone is often seen with orally supplemented progesterone, as the liver metabolizes a large portion of oral progesterone to the neuroactive steroid allopregnanolone.

Progesterone (Post-menopausal)
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