Remission of subclinical adrenocortical failure in subjects with adrenal autoantibodies.
Abstract
Idiopathic Addison's disease is a chronic organ-specific autoimmune disorder with a long subclinical period characterized only by the presence of adrenal autoantibodies (AA) with or without adrenal function failure. The aim of this longitudinal study was to evaluate the behavior of AA using, an indirect fluorescence method, and adrenal function in 20 AA-positive and 50 AA-negative patients screened by an investigation of a large population of organ-specific autoimmune disease patients without clinical Addison's disease. As controls, 100 normal age-matched subjects were tested only once. In the 20 AA-positive and 50 negative patients, AA and adrenal functional tests were evaluated every 4 months for 5 yr. The AA-positive patients were grouped into 5 adrenal functional stages, specifically: stage 0, normal adrenal function; stage 1, high PRA and low (or normal) aldosterone levels alone; stage 2, along with impaired cortisol response to ACTH, stage 3, along with increased ACTH levels; and stage 4, clinically overt Addison's disease. On the basis of the behavior of AA, the 20 positive patients were grouped as follows: group A, 11 patients with AA titer of 1:8 or higher at the first observation and persistently AA positive in subsequent observations, with titers ranging from 1:8 to 1:64; group B, 6 patients with initial AA titers of 1:8 or lower and AA disappearance in subsequent observations; and group C, 3 patients with AA titer of 1:32 or higher, undergoing corticosteroid thera…
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An elevated plasma renin activity or concentration with an inappropriately normal or low serum aldosterone concentration is suggestive of PAI.
“Thus, an elevated plasma renin activity or concentration in combination with an (inappropriately) normal or low serum aldosterone concentration is suggestive of PAI (38,(71)(72)(73)(74).”
From Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline (2016) · cites this paper as [73]
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Addison’s Disease and Autoimmune Polyglandular Syndromes
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Use of serum pituitary antibodies to improve the diagnosis of hypophysitis
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Self-citation
- Authors
- De Bellis, A., Bizzarro, A., Rossi, R., Paglionico, V. A., Criscuolo, T., Lombardi, G., & Bellastella, A.
- Affiliations
- University of Naples Federico II (IT)
- ORCID
- Bellastella, A
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 1993-04
- Volume
- 76
- Issue
- 4
- Pages
- 1002-1007
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- OpenAlex
- W2148524987
- Cited by
- 106
- References
- 17
- Citations by year
- 2022: 1 · 2019: 5 · 2018: 2 · 2017: 2 · 2016: 4 · 2015: 1 · 2014: 2 · 2013: 3 · 2012: 5
- FWCI
- 2.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli" (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal Regulation and Hypertension
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- Addison's disease, adrenal autoantibodies, remission, autoimmune adrenal insufficiency, adrenal function recovery, corticosteroid therapy, ACTH stimulation test, antibody titer decline, disease progression, organ-specific autoimmunity, indirect immunofluorescence
- MeSH terms
- Addison Disease, Adolescent, Adrenal Cortex, Adrenal Cortex Function Tests, Adrenal Cortex Hormones, Adrenal Insufficiency, Adrenal Glands, Adult, Autoantibodies, Child, Female, Humans, Longitudinal Studies, Male, Time Factors
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