Addison Disease
"Addison Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES.
Descriptor ID |
D000224
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MeSH Number(s) |
C19.053.500.263 C20.111.163
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Concept/Terms |
Addison Disease- Addison Disease
- Disease, Addison
- Primary Adrenal Insufficiency
- Adrenal Insufficiency, Primary
- Primary Hypoadrenalism
- Hypoadrenalism, Primary
- Hypoadrenalisms, Primary
- Addison's Disease
- Addisons Disease
- Primary Adrenocortical Insufficiency
- Adrenocortical Insufficiencies, Primary
- Adrenocortical Insufficiency, Primary
- Insufficiencies, Primary Adrenocortical
- Insufficiency, Primary Adrenocortical
- Primary Adrenocortical Insufficiencies
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Below are MeSH descriptors whose meaning is more general than "Addison Disease".
Below are MeSH descriptors whose meaning is more specific than "Addison Disease".
This graph shows the total number of publications written about "Addison Disease" by people in this website by year, and whether "Addison Disease" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1999 | 1 | 0 | 1 | 2002 | 0 | 2 | 2 | 2004 | 1 | 0 | 1 | 2005 | 0 | 1 | 1 | 2009 | 1 | 0 | 1 | 2010 | 1 | 0 | 1 | 2011 | 1 | 0 | 1 | 2012 | 2 | 1 | 3 | 2014 | 2 | 0 | 2 | 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Addison Disease" by people in Profiles.
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Regan EA, Vaidya A, Margulies PL, Make BJ, Lowe KE, Crapo JD. Primary adrenal insufficiency in the United States: diagnostic error and patient satisfaction with treatment. Diagnosis (Berl). 2019 11 26; 6(4):343-350.
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Ross IL, Babu S, Armstrong T, Zhang L, Schatz D, Pugliese A, Eisenbarth G, Baker Ii P. HLA similarities indicate shared genetic risk in 21-hydroxylase autoantibody positive South African and United States Addison's disease. Tissue Antigens. 2014 Oct; 84(4):361-9.
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Michels A, Michels N. Addison disease: early detection and treatment principles. Am Fam Physician. 2014 Apr 01; 89(7):563-8.
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Baker P, Fain P, Kahles H, Yu L, Hutton J, Wenzlau J, Rewers M, Badenhoop K, Eisenbarth G. Genetic determinants of 21-hydroxylase autoantibodies amongst patients of the Type 1 Diabetes Genetics Consortium. J Clin Endocrinol Metab. 2012 Aug; 97(8):E1573-8.
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Baker PR, Nanduri P, Gottlieb PA, Yu L, Klingensmith GJ, Eisenbarth GS, Barker JM. Predicting the onset of Addison's disease: ACTH, renin, cortisol and 21-hydroxylase autoantibodies. Clin Endocrinol (Oxf). 2012 May; 76(5):617-24.
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Barker JM. Compounding risk for hypoglycemia: type 1 diabetes and Addison's disease. Diabetes Technol Ther. 2012 May; 14(5):383-5.
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Baker PR, Baschal EE, Fain PR, Nanduri P, Triolo TM, Siebert JC, Armstrong TK, Babu SR, Rewers MJ, Gottlieb PA, Barker JM, Eisenbarth GS. Dominant suppression of Addison's disease associated with HLA-B15. J Clin Endocrinol Metab. 2011 Jul; 96(7):2154-62.
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Baker PR, Baschal EE, Fain PR, Triolo TM, Nanduri P, Siebert JC, Armstrong TK, Babu SR, Rewers MJ, Gottlieb PA, Barker JM, Eisenbarth GS. Haplotype analysis discriminates genetic risk for DR3-associated endocrine autoimmunity and helps define extreme risk for Addison's disease. J Clin Endocrinol Metab. 2010 Oct; 95(10):E263-70.
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Triolo TM, Baschal EE, Armstrong TK, Toews CS, Fain PR, Rewers MJ, Yu L, Miao D, Eisenbarth GS, Gottlieb PA, Barker JM. Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes. J Clin Endocrinol Metab. 2009 Nov; 94(11):4517-23.
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Laberge G, Mailloux CM, Gowan K, Holland P, Bennett DC, Fain PR, Spritz RA. Early disease onset and increased risk of other autoimmune diseases in familial generalized vitiligo. Pigment Cell Res. 2005 Aug; 18(4):300-5.
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