Evidence map›Paper›PMID 34665570›Full record

ArticleEuropean journal of endocrinology2021

The natural history of 21-hydroxylase autoantibodies in autoimmune Addison's disease.

Anette Boe Wolff, Lars Breivik, Karl Ove Hufthammer, Marianne Aardal Grytaas, Eirik Bratland, Eystein Sverre Husebye, Bergithe Eikeland Oftedal

Open access · hybridAbstract read
In one paragraph

Article in European journal of endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Aire Mutations and Autoimmune Diseases.Advances in experimental medicine and biology · 2025
    Review
  6. Regulatory T cells in autoimmune primary adrenal insufficiency.Clinical and experimental immunology · 2024
    Article
  7. Article
  8. Approach to the Patient: Diagnosis of Primary Adrenal Insufficiency in Adults.The Journal of clinical endocrinology and metabolism · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Primary Ovarian Insufficiency in Women With Addison's Disease.The Journal of clinical endocrinology and metabolism · 2021
    Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Anette Boe WolffDepartment of Clinical Science, University of Bergen, Norway.ORCID 0000-0002-8485-2248
Lars BreivikDepartment of Clinical Science, University of Bergen, Norway.
Karl Ove HufthammerCentre for Clinical Research, University of Bergen, Norway.ORCID 0000-0003-3170-9496
Marianne Aardal GrytaasK.G. Jebsen Center for autoimmune disorders, University of Bergen, Norway.ORCID 0000-0001-9016-628X
Eirik BratlandDepartment of Clinical Science, University of Bergen, Norway.
Eystein Sverre HusebyeDepartment of Clinical Science, University of Bergen, Norway.
Bergithe Eikeland OftedalDepartment of Clinical Science, University of Bergen, Norway.
University of Bergen · NOHaukeland University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe most common cause of primary adrenal failure (Addison's disease) in the Western world is autoimmunity characterized by autoantibodies against the steroidogenic enzyme 21-hydroxylase (CYP21A2, 21OH). Detection of 21OH-autoantibodies is currently used for aetiological diagnosis, but how levels of 21OH-autoantibodies vary over time is not known.

settingSamples from the national Norwegian Addison's Registry and Biobank established in 1996 (n = 711). Multi-parameter modelling of the course of 21OH-autoantibody indices over time.

results21OH-autoantibody positivity is remarkably stable, and >90% of the patients are still positive 30 years after diagnosis. Even though the antibody levels decline with disease duration, it is only rarely that this downturn reaches negativity. 21OH-autoantibody indices are affected by age at diagnosis, sex, type of Addison's disease (isolated vs autoimmune polyendocrine syndrome type I or II) and HLA genotype.

conclusion21OH-autoantibodies are reliable and robust markers for autoimmune Addison's disease, linked to HLA risk genotype. However, a negative test in patients with long disease duration does not exclude autoimmune aetiology.

Indexed as

Addison DiseaseAdolescentAdultAutoantibodiesBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedSteroid 21-HydroxylaseYoung AdultAutoantibodiesBiomarkersSteroid 21-Hydroxylase

Identifiers

PMID34665570
PMCPMC8052519
OpenAlexW3127255953

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.