Evidence map›Paper›PMID 41890739›Full record

Observational studyFrontiers in immunology2026

Low serum IgE is associated with an increased risk of chronic lymphocytic leukemia: a large retrospective cohort study.

Ramon Cohen, Daniel Elbirt, Shay Nemet, Alena Kirzhner, Tal Schiller, Haitham Abu Khadija, Shira Bezalel-Rosenberg, Ilan Asher, Keren Mahlab-Guri, Ofir Wolach and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 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

11 authors.

Ramon Cohen *Department of Internal Medicine B, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Daniel Elbirt *Department of Clinical Immunology, Allergy and AIDS, Kaplan Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Shay NemetDepartment of Clinical Immunology, Allergy and AIDS, Kaplan Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Alena KirzhnerDepartment of Internal Medicine A, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Tal SchillerInstitute of Endocrinology, Diabetes and Metabolic disease, Wolfson Medical Center, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Haitham Abu KhadijaDepartment of Cardiology, Kaplan Medical Center and Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Shira Bezalel-RosenbergDepartment of Clinical Immunology, Allergy and AIDS, Kaplan Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Ilan AsherDepartment of Clinical Immunology, Allergy and AIDS, Kaplan Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Keren Mahlab-GuriDepartment of Clinical Immunology, Allergy and AIDS, Kaplan Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Ofir WolachInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Liron HofstetterInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic lymphocytic leukemia (CLL) is the most prevalent adult leukemia in the western world. Its pathophysiology is intertwined with immune dysfunction. Emerging evidence suggests an inverse association between serum immunoglobulin E (IgE) and hematologic malignancies, but previous studies linking low IgE to CLL risk were limited by small cohorts and a lack of adjustment for confounding factors, particularly hypogammaglobulinemia. Purpose: This study aimed to evaluate the association between low serum IgE levels and the future development of CLL in a large, real-world cohort, while accounting for other immunoglobulins and confounding factors. Methods: We conducted a retrospective quantitative observational study of 118,740 adults from a large health maintenance organization. The primary exposure was a baseline IgE level of less than 25 IU/mL. We used Kaplan-Meier curves and a multivariable Cox proportional hazards model to assess the association between low IgE and CLL diagnosis over a seven-year follow-up period, adjusting for age, sex, and other potential confounders, including hypogammaglobulinemia and atopy-related conditions. Results: A serum IgE level of less than 25 IU/mL was significantly associated with an increased hazard of developing CLL (HR = 1.94, 97.5% CI: 1.47-2.56). This association persisted after adjusting for all confounding variables. Established risk factors, such as older age (HR = 1.07) and male sex (HR = 1.82), were also significant. Kaplan-Meier curves showed a sustained and a statistically significant increased risk in the low IgE group throughout the follow-up period. Conclusion: Lower serum IgE levels are independently associated with an increased risk of developing CLL.

Indexed as

Immunoglobulin ELeukemia, Lymphocytic, Chronic, B-CellAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsImmunoglobulin Eatopychronic lymphocytic leukemiaCLLIgEleukemia

Identifiers

PMID41890739
PMCPMC13013483

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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.