Evidence map›Paper›PMID 41798765›Full record

ReviewThe World Allergy Organization journal2026

Non-syndromic hyper-IgE in children: A practical approach.

Riccardo Castagnoli, Luca Pecoraro, Carla Mastrorilli, Stefania Arasi, Simona Barni, Lucia Caminiti, Mariannita Gelsomino, Mattia Giovannini, Angela Klain, Lucia Liotti and 7 more

Abstract readReview
In one paragraph

Review in The World Allergy Organization journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Non-syndromic elevated IgE.The World Allergy Organization journal · 2026
    Article
  3. Article
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

17 authors.

Riccardo CastagnoliPediatric Unit, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, 27100, Italy.
Luca PecoraroPediatric Unit, Ospedale Vito Fazzi, ASL Lecce, 73100 Lecce, Italy.
Carla MastrorilliPediatric and Emergency Department, Pediatric Hospital Giovanni XXIII, AOU Policlinic of Bari, Bari, 70126, Italy.
Stefania ArasiDivision of Allergy, Translational Research in Pediatric Specialties Area, Bambino Gesù Children's Hospital, IRCCS, Rome, 00165, Italy.
Simona BarniAllergy Unit, Meyer Children's Hospital IRCCS, Florence, 50139, Italy.
Lucia CaminitiAllergy Unit, Department of Pediatrics, AOU Policlinico Gaetano Martino, Messina, 98124, Italy.
Mariannita GelsominoDepartment of Life Sciences and Public Health, Pediatric Allergy Unit, University Foundation Policlinico Gemelli IRCCS Catholic University of the Sacred Heart Rome, Rome, Italy.
Mattia GiovanniniAllergy Unit, Meyer Children's Hospital IRCCS, Florence, 50139, Italy.
Angela KlainDepartment of Woman, Child and General and Specialized Surgery, University of Campania "Luigi Vanvitelli", Naples, 80138, Italy.
Lucia LiottiDepartment of Mother and Child Health, Pediatric Unit, Salesi Children's Hospital, Ancona, 60123, Italy.
Francesca MoriAllergy Unit, Meyer Children's Hospital IRCCS, Florence, 50139, Italy.
Francesca SarettaPediatric Department, General Pediatrician, Azienda Sanitaria Universitaria Friuli Centrale, Udine, 33100, Italy.
Fabio CardinalePediatric and Emergency Department, Pediatric Hospital Giovanni XXIII, AOU Policlinic of Bari, Bari, 70126, Italy.
Michele Miraglia Del GiudiceDepartment of Woman, Child and General and Specialized Surgery, University of Campania "Luigi Vanvitelli", Naples, 80138, Italy.
Gian Luigi MarsegliaPediatric Unit, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, 27100, Italy.
Elio NovembreDepartment of Health Sciences, University of Florence, Florence, 50139, Italy.
Rare Allergic Diseases Task Force of the Italian Society of Pediatric Allergy and Immunology (SIAIP)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyper-IgE, generally defined as serum IgE levels exceeding 2000 IU/mL, presents a common yet complex diagnostic challenge in pediatric practice. While elevated serum IgE are frequently observed in atopic conditions such as food allergy or atopic eczema, or parasitic infections, they may also signal underlying monogenic immunological diseases, specifically inborn errors of immunity (IEI) categorized under hyper-IgE syndrome (HIES). Distinguishing between common atopic diseases and HIES is essential, especially in children with early-onset, severe, or treatment-resistant presentations. This review focuses on non-syndromic causes of hyper-IgE in children, aiming to provide a practical, structured framework for clinicians. A broad array of conditions, including allergic diseases, infections, inflammatory disorders, malignancies, drug reactions, and environmental exposures, can result in elevated IgE levels. Given this wide differential, a systematic approach that incorporates detailed clinical history, physical examination, and targeted investigations is critical to guide diagnostic reasoning. To aid clinical decision-making, the authors propose a stepwise diagnostic algorithm that prioritizes common causes while also alerting clinicians to red flags suggestive of IEI or other rare conditions. This approach facilitates timely referral for immunologic or genetic evaluation when appropriate and minimizes unnecessary testing. Increased awareness of the diverse etiologies of hyper-IgE can improve diagnostic accuracy, enhance early intervention, and reduce morbidity. Future research should aim to refine diagnostic strategies, validate clinical algorithms, and develop standardized guidelines. Moreover, long-term data regarding characterization and subsequent follow-up of children with an isolated increase in serum IgE levels is fundamental to understanding the clinical and immunological trajectories of these patients.

Indexed as

allergyatopyElevated IgE levelsHyper-IgEInborn errors of immunityparasitic infections

Identifiers

PMID41798765
PMCPMC12963907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.