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GlossaryACTH Stimulation Test (ACTH Test)

measures adrenal gland response to synthetic ACTH injection

The ACTH Stimulation Test, also known as the Adrenocorticotropic Hormone Stimulation Test, is a diagnostic procedure used to assess the functioning of the adrenal glands. During the test, synthetic ACTH is administered to stimulate the adrenal glands to produce cortisol, and blood samples are taken to measure cortisol levels before and after the injection. This helps diagnose conditions like Addison's disease or adrenal insufficiency.

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Results of Clinical Examinations, Laboratory Tests, and Ultrasonography in Dogs with Pituitary-Dependent Hyperadrenocorticism Treated with Trilostane

research Results of Clinical Examinations, Laboratory Tests, and Ultrasonography in Dogs with Pituitary-Dependent Hyperadrenocorticism Treated with Trilostane

116 citations, April 2002 in “American journal of veterinary research”

Trilostane effectively and safely treats dogs with pituitary-dependent hyperadrenocorticism, improving symptoms and adrenal gland size.

Urinary 5-Ene-Steroid Excretion in Non-Classical Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Deficiency

research Urinary 5-Ene-Steroid Excretion in Non-Classical Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Deficiency

3 citations, May 1990 in “Journal of Steroid Biochemistry”

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Adrenal 21-Hydroxylase Gene Mutations in Slovenian Hyperandrogenic Women: Evaluation of Corticotrophin Stimulation and HLA Polymorphisms in Screening for Carrier Status

research Adrenal 21-Hydroxylase Gene Mutations in Slovenian Hyperandrogenic Women: Evaluation of Corticotrophin Stimulation and HLA Polymorphisms in Screening for Carrier Status

19 citations, August 1999 in “European journal of endocrinology”

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

research Congenital Adrenal Hyperplasia: A Comprehensive Review

88 citations, April 2017 in “Journal of Pediatric and Adolescent Gynecology”

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

research Recommendations for Treatment of Nonclassic Congenital Adrenal Hyperplasia: An Update

56 citations, December 2011 in “Steroids”

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

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community How does hair loss and recovery work?

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Hair loss varies due to genetic sensitivity to DHT and other factors. Treatments discussed include finasteride, minoxidil, RU58841, and microneedling.