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. 2025 Jan 9;4(2):100403.
doi: 10.1016/j.jacig.2025.100403. eCollection 2025 May.

Clinical significance of very high IgE levels (≥1000 IU/mL): Population-based study of 118,211 adults

Affiliations

Clinical significance of very high IgE levels (≥1000 IU/mL): Population-based study of 118,211 adults

Shay Nemet et al. J Allergy Clin Immunol Glob. .

Abstract

Background: Very high serum IgE (≥1000 IU/mL) is reported in atopic disorders. However, data on its significance in nonallergic disorders are limited.

Objective: We aimed to analyze the diagnostic value of very high IgE in adults.

Methods: A retrospective nationwide study was conducted using the electronic database of Clalit Health Services, covering adults (≥18 years) treated between 2002 and 2022. Subjects with IgE ≥ 1000 IU/mL were compared to the controls with IgE < 100 IU/mL across 3 age groups (18-30, 31-64, and ≥65 years). Outcomes included eosinophilic, autoimmune, autoinflammatory, and cardiovascular disorders (CVD), cancer, and inborn errors of immunity (IEI). A multivariable Cox regression model determined statistical significance (P < .05).

Results: The study included 118,211 subjects: 110,116 controls and 8635 with very high IgE levels. Excluding insect sting and drug allergies, very high IgE was more common across all tested allergic disorders, with asthma showing the highest rate (64.49%). Univariable analysis showed higher prevalence of CVD (3.88% vs 2.72%, P < .001), eosinophilic disorders (0.42% vs 0.06%, P < .001), and IEI (0.35% vs 0.20%, P = .004) in the very high IgE group. Multivariable analysis revealed age-dependent significant results: higher CVD risk in ages 31-64 (hazard ratio = 1.249; 95% confidence interval, 1.054-1.481; P = .010) and borderline IEI association in ages 18-30 (hazard ratio = 1.802; 95% confidence interval, 0.978-3.321; P = .059). Risk of eosinophilic disorders was increased across all age groups (P < .001).

Conclusions: Very high IgE level of ≥1000 IU/mL is associated with increased risks of CVD, IEI, and eosinophilic disorders. Physicians should consider further assessment for these conditions in nonallergic patients with very high IgE levels.

Keywords: IgE; immunoglobulin E; population-based study; very high IgE.

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Conflict of interest statement

Supported in part by grant from the Israeli Association of Allergy and Clinical Immunology. Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest.

Figures

Fig 1
Fig 1
Kaplan-Meier curves illustrating cumulative risk of developing various outcomes in subjects with very high IgE levels compared to controls. Presented are Kaplan-Meier curves for outcomes demonstrating statistically significant associations in the univariable analysis. Pale blue indicates control group; green, very high IgE (≥1000 IU/mL) group. (A-C) Risk of developing CVD in age groups 18-30, 31-64, and ≥65 years, respectively. (D-F) Risk of developing eosinophilic disorders in age groups 18-30, 31-64, and ≥65 years, respectively. (G-I) Risk of being diagnosed with IEI in the age group of 18-30, 31-64, and ≥65 years, respectively.
Fig 2
Fig 2
Suggested algorithm for clinical management of asymptomatic adult patients with serum IgE ≥ 1000 IU/mL. First, rule out allergic disorders such as atopic dermatitis and asthma, as well as parasitic infections. Management then depends on patient’s age group. Screening for eosinophilic disorders, including CBC, should be conducted in all age groups. For young adults (18-30 years), investigate IEI by first looking for red flags, then performing basic immune assessment. For patients aged 31-64 years with IgE ≥ 1000 IU/mL, follow guidelines for assessing 10-year CVD risk and treat other CVD risk factors accordingly.CBC, Complete blood count; LDL, low-density lipoprotein; SBP, systolic blood pressure.

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