# Severe eosinophilia and risk of major disease and mortality: A nationwide cohort study of children and adults

**Authors:** Shay Nemet, Daniel Elbirt, Ramon Cohen, Keren Mahlab-Guri, Vered Shkalim Zemer, Ilan Asher, Aviv Talmon, Limor Rubin, Yaarit Ribak, Eyal Ben-Dori, Inon Sarig, Nur Sagi, Ruslan Sergienko, Yuval Tal, Oded Shamriz

PMC · DOI: 10.1016/j.jacig.2026.100654 · The Journal of Allergy and Clinical Immunology: Global · 2026-02-04

## TL;DR

Severe eosinophilia is linked to higher risks of serious diseases and early death in both children and adults, highlighting the need for thorough medical evaluation.

## Contribution

This study is the first to comprehensively assess long-term risks of severe eosinophilia across age groups using a nationwide cohort.

## Key findings

- Severe eosinophilia in adults is associated with increased risks of hematologic malignancy, autoimmune disease, and mortality.
- In children, severe eosinophilia is strongly linked to solid tumors, autoimmune disease, and significantly higher mortality.
- Both adult and pediatric patients with severe eosinophilia face elevated risks of thromboembolic events and allergic disorders.

## Abstract

Severe eosinophilia (SE), defined as greater than 5000 cells/μL, is uncommon but may indicate serious underlying disease. Its long-term prognostic implications across age groups remain unclear.

We sought to investigate the long-term risk of morbidity and all-cause mortality in children and adults with SE.

We conducted a nationwide, population-based, matched cohort study using data from Clalit Health Services, Israel (2000-2023). Individuals with SE (n = 3822) were matched 1:10 to subjects without SE with normal eosinophil counts (<500/μL; n = 39,005). Five-year risks of cancer, autoimmune disease, thromboembolic events, allergic disorders, and all-cause mortality were assessed using multivariable Cox proportional hazards models.

The study included 42,827 participants, both with and without SE. Among the 29,289 adults, 2,497 had SE and 26,792 did not. Among the 13,538 children, 1,325 had SE and 12,213 did not. Among adults, SE was associated with increased risk of hematologic malignancy (hazard ratio [HR], 2.86; 95% CI, 1.88-4.36), autoimmune disease (HR, 1.64; 95% CI, 1.38-1.95), thromboembolic events (HR, 1.91; 95% CI, 1.45-2.53), and mortality (HR, 2.20; 95% CI, 1.84-2.62). In children, SE predicted solid tumors (HR, 14.24; 95% CI, 2.39-85.00), autoimmune disease (HR, 2.48; 95% CI, 1.97-3.12), allergic disorders (HR, 1.45; 95% CI, 1.26-1.67), and markedly increased mortality (HR, 7.95; 95% CI, 3.23-19.56).

Severe eosinophilia is a strong prognostic marker in both children and adults, associated with malignancy, autoimmune and thromboembolic disease, and premature death. Recognition of SE should prompt comprehensive evaluation and close follow-up in general and specialty caregivers.

## Linked entities

- **Diseases:** hematologic malignancy (MONDO:0002334), autoimmune disease (MONDO:0007179)

## Full-text entities

- **Genes:** CD40LG (CD40 ligand) [NCBI Gene 959] {aka CD154, CD40L, HIGM1, IGM, IMD3, T-BAM}, RNASE3 (ribonuclease A family member 3) [NCBI Gene 6037] {aka ECP, RAF1, RNS3}, EPX (eosinophil peroxidase) [NCBI Gene 8288] {aka EPO, EPP, EPX-PEN, EPXD}, AICDA (activation induced cytidine deaminase) [NCBI Gene 57379] {aka AID, ARP2, CDA2, HEL-S-284, HIGM2}, THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Paraneoplastic SE (MESH:D045169), head and neck squamous cell carcinoma (MESH:D000077195), tissue injury (MESH:D017695), Hematologic malignancies (MESH:D019337), oncologic (MESH:D000072716), immune dysregulation (OMIM:614878), Autoinflammatory disorders (MESH:D056660), atopic disorders (MESH:D006969), carcinogenesis (MESH:D063646), parasitic (MESH:D010272), allergic (MESH:D004342), TEDs (MESH:D013923), chronic eosinophilic vasculitis (MESH:C580364), lymphocytic leukemias (MESH:D007945), AIDs (MESH:D001327), skin cancers (MESH:D012878), inflammatory bowel disease (MESH:D015212), colorectal and breast cancer (MESH:D001943), lymphoma (MESH:D008223), asthma (MESH:D001249), Eosinophilia (MESH:D004802), CHS (OMIM:603663), venous thrombosis (MESH:D020246), cytotoxicity (MESH:D064420), Inborn errors of immunity (MESH:D007154), malignancies (MESH:D009369), end-organ damage (MESH:C564816), adrenal insufficiency (MESH:D000309), systemic symptoms syndrome (MESH:D063926), multiple myeloma (MESH:D009101), helminthic infections (MESH:D007239), leukemia (MESH:D007938), Hypereosinophilic syndrome (MESH:D017681), eosinophilic granulomatosis with polyangiitis (MESH:D014890), strongyloidiasis (MESH:D013322), myelogenous leukemias (MESH:D007951), immunodeficiency (MESH:D007153), death (MESH:D003643), fibrosis (MESH:D005355), atopic (MESH:C566404), thrombotic (MESH:D013927), metastases (MESH:D009362), CCI (MESH:C566784), inflammation (MESH:D007249)
- **Species:** Strongyloides (genus) [taxon 6247], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968414/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968414/full.md

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Source: https://tomesphere.com/paper/PMC12968414