Pregnenolone is a precursor to many critical steroid hormones in our bodies including:
Pregnenolone as a supplement:
Pregnenolone can be valuable as an alternative treatment for improving memory and alertness, while reducing stress, depression and fatigue. Although the current research is inconclusive there are also claims that the hormone helps to prevent cancer, obesity, arthritis, multiple sclerosis, premenstrual syndrome and menopause. Pregnenolone levels decline more than 60% as we age. Chemically modified or synthetic pregnenolone supplements are taken to counteract some of the typical signs of aging and increase the levels of DHEA and other steroid hormones, including testosterone, in the body. High levels can cause adverse side effects such as aggression, irritability, insomnia, and the growth of body or facial hair in women. Pregnant women should not take pregnenolone.
Pregnenolone and congenital adrenal hyperplasia (CAH)
High pregnenolone levels may be caused by an inherited condition called congenital adrenal hyperplasia (CAH). CAH causes a deficiency or dysfunction in the enzymes required to convert pregnenolone into steroid hormones. This can cause a deficiency of cortisol and an overabundance of male hormones or androgens. The pregnenolone test is often used in suspected cases of CAH for infants whose external sex organs are not clearly defined or for teens who do not develop secondary sexual characteristics or who has delayed puberty. If there is an enzyme deficiency in the steroid hormone process the levels of pregnenolone may be elevated. This can help to determine which enzyme is deficient or defective.
What is congenital adrenal hyperplasia (CAH)?
CAH is a group of inherited disorders associated with deficiencies in the enzymes required for the production of the steroid hormones.
In congenital adrenal hyperplasia, one or more of the enzymes is deficient or dysfunctional and inadequate amounts of one or more final products are produced.
With CAH, the enzyme deficiency can cause a decrease in cortisol and/or aldosterone and, in some cases, an increase or decrease in androgens. Deficient androgens can cause male newborns to be born with external sex organs that are not clearly male or female (ambiguous genitalia) and can affect the development of secondary sexual characteristics of both males and females at puberty.
What are the causes of CAH?
Congenital adrenal hyperplasia (CAH) is caused by inherited defects in steroid biosynthesis. The resulting hormone imbalances can lead to life-threatening, salt-wasting crisis in the newborn period and incorrect gender assignment of virilized females.
What are the various Pregnenolone reference values?
or =18 years: 33-248 ng/dL
Pregnenolone levels naturally decrease as a person ages. A deficiency in pregnenolone can result in deficiency in other hormones. Symptoms can include decreased sex drive, depression, fatigue, impaired memory, loss of bone density and decreased muscle mass.
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Pregnenolone is used by the body in the production of all steroid hormones such as estrogen, progesterone, cortisol and testosterone. Pregnenolone is typically tested to aid in diagnosing a condition known as Congenital Adrenal Hyperplasia (CAH). CAH is a group of disorders in which the body is deficient in one or more of the enzymes required to produce steroid hormones.
Elevated levels of pregnenolone typically indicate that one or more of these enzymes is deficient.
Infants with CAH may show symptoms such as high blood pressure, extreme loss of fluids or sex organs which are not clearly defined.
Teens may experience delayed puberty, acne, oily skin and high blood pressure.
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5-Methyltetrahydrofolate, Adiponectin, Albumin/Creatinine Ratio, Random Urine, Anti-Thyroglobulin ab. (0-39), C-Peptide, Serum, Ceruloplasmin, Creatinine, Random Urine, Cyclic AMP, Plasma, Dihydrotestosterone (female), Dihydrotestosterone (male), Estimated Average Glucose (eAG), Free Androgen Index, Free testosterone, Free Testosterone, Direct (Female), Free Testosterone, Direct (Male), Free Thyroxine, Free Thyroxine Index, Fructosamine, Glucose, Glutamic Acid Decarboxylase, Glycated Serum Protein (GSP), Hemoglobin A1c (HbA1c), HOMA-B, HOMA-IR, HOMA-S, Homocysteine, Insulin (Fasting), Insulin Antibody, Insulin-Like Growth Factor I (IGF-1), Iodine, Serum/Plasma, Parathyroid Hormone (PTH), Serum, Pregnenolone, Proinsulin, Reverse T3, Serum, Sex Hormone-Binding Globulin (SHBG), T3, Free, T4, Free, T4, Total (Thyroxine), T7 Index, Testosterone, Testosterone (Female/Child), Testosterone, Serum (Female), Thyroglobulin, Thyroglobulin Antibodies (0 - 1 IU/L), Thyroid Peroxidase Antibodies (Anti-TPO Ab), Thyroid Stim Immunoglobulin, Thyroid-Stimulating Hormone (TSH), Thyrotropin Receptor Ab, Serum, Thyroxine-binding globulin, TBG, TMAO (Trimethylamine N-oxide), Total T3, Tri iodothyronine (T3) Uptake, Triiodothyronine, Serum