Evidence map›Paper›PMID 42484378›Full record

ArticleJCI insight2026

Performance of expanded diagnostic criteria for APECED in independent cohorts and implications for earlier diagnosis.

Elise Mn Ferré, Joseph Pechacek, Monica M Schmitt, Taura Webb, Heather Moorman, Thomas DiMaggio, Princess Barber, Vasielios Oikonomou, Stacey R Rose, Peter D Burbelo and 26 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

36 authors.

Elise Mn FerréFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Joseph PechacekFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Monica M SchmittFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Taura WebbFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Heather MoormanFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Thomas DiMaggioFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Princess BarberFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Vasielios OikonomouFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Stacey R RoseFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).
Peter D BurbeloAdeno-Associated Virus Biology Section, National Institute of Dental and Craniofacial Research (NIDCR).
Lindsey B RosenImmunopathogenesis Section, LCIM, NIAID.
Amy P HsuImmunopathogenesis Section, LCIM, NIAID.
Jennifer StoddardImmunology Service, Department of Laboratory Medicine (DLM), Clinical Center.
Shakuntala RampertaapImmunology Service, Department of Laboratory Medicine (DLM), Clinical Center.
Sergio D RosenzweigImmunology Service, Department of Laboratory Medicine (DLM), Clinical Center.
Anjali RaiTranslational Hepatology Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
Maria Teresa MagoneConsult Services Section, National Eye Institute.
Chantal Cousineau-KriegerConsult Services Section, National Eye Institute.
Niki M MoutsopoulosHuman Barrier Immunity Section, Laboratory of Host Immunity & Microbiome, NIAID.
Pamela J GardnerDental Consult Services, NIDCR.
Heidi H KongCutaneous Microbiome and Inflammation Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases.
Leslie Castelo-SoccioCutaneous Microbiome and Inflammation Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases.
Ariane SoldatosPediatric Neurology Consultation Service, Office of the Clinical Director, National Institute of Neurological Disorders and Stroke.
Katherine R CalvoHematology Laboratory Service, DLM, Clinical Center.
Meryl WaldmanClinical Nephrology Section, Kidney Diseases Branch, NIDDK.
Behdad AfzaliClinical Nephrology Section, Kidney Diseases Branch, NIDDK.
Stefania PittalugaLaboratory of Pathology, National Cancer Institute.
David KleinerLaboratory of Pathology, National Cancer Institute.
Steven M HollandImmunopathogenesis Section, LCIM, NIAID.
Kevin FennellyLaboratory of Chronic Airway Infection, Critical Care Medicine and Pulmonary Branch, National Heart, Lung, and Blood Institute.
Jill RothschildPediatric Hospitalist Section, Department of Pediatrics.
Bryce A SeifertDivision of Intramural Research, NIAID, and.
Magdalena Walkiewicz-YvonDivision of Intramural Research, NIAID, and.
Theo HellerTranslational Hepatology Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
Karen WinerPediatric Growth and Nutrition Branch, National Institute of Child Health and Human Development, NIH, Bethesda, Maryland, USA.
Michail S LionakisFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID).

Funding

Immunopathogenesis of Fungal InfectionsZIAAI001175 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LIONAKIS, MICHAIL · 2012 to 2025
$23.9M
Intramural NIH HHS ZIA AI001175
6 · The paper itself

Abstract

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED/APS-1) is a monogenic autoimmune disorder of impaired central tolerance classically diagnosed by the presence of 2 out of 3 classic triad manifestations: chronic mucocutaneous candidiasis, hypoparathyroidism, and adrenal insufficiency. However, many patients develop non-triad manifestations years earlier, delaying recognition and care. In 2016, we proposed expanded diagnostic criteria incorporating 3 early clinical manifestations - APECED rash, autoimmune enteritis, and enamel hypoplasia - based on observations in 35 North American patients. Here, we provide further support for the clinical utility of these expanded diagnostic criteria in independent cohorts of 57 American and 12 European patients enrolled in a prospective natural history study at the NIH. Across all cohorts, the expanded diagnostic criteria decreased the time to diagnosis by half relative to the classic diagnostic criteria. Patients exhibited an enrichment of early non-endocrine autoimmune manifestations, underscoring disease heterogeneity and the potential for developing organ-specific autoimmunity before endocrine failure. These findings demonstrate the clinical utility of the expanded APECED diagnostic criteria and support the notion that their adoption might enable earlier disease recognition and timely immunomodulatory therapy to improve long-term outcomes.

Indexed as

Polyendocrinopathies, AutoimmuneAdolescentAdultChildChild, PreschoolCohort StudiesDental Enamel HypoplasiaEarly DiagnosisFemaleHumansMaleProspective StudiesYoung AdultAutoimmune diseasesAutoimmunityClinical ResearchGenetic diseasesImmunologyT cells

Identifiers

PMID42484378
PMCPMC13461156

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.