Evidence map›Paper›PMID 41673825›Full record

ArticleBMC immunology2026

Pretreatment immunoglobulin profiles and survival outcomes in hematologic malignancies and autoimmune cytopenias: a comparative cohort analysis.

Mehmet Emin Gerek, Atakan Tekinalp, Fatih Çölkesen, Tuğba Önalan, Fatma Arzu Akkuş, Mehmet Kılınç, Selim Kahraman, Şevket Arslan

Abstract readComparative Study
In one paragraph

Article in BMC immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Mehmet Emin GerekDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University Faculty of Medicine, Akyokuş, Meram/Konya, 42080, Türkiye.
Atakan TekinalpDepartment of Internal Medicine, Division of Hematology, Necmettin Erbakan University Faculty of Medicine, Konya, Türkiye.
Fatih ÇölkesenDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University Faculty of Medicine, Akyokuş, Meram/Konya, 42080, Türkiye. neueriskinimmunoloji@gmail.com.
Tuğba ÖnalanDepartment of Internal Medicine, Division of Clinical Immunology and Allergy, Beyhekim Training and Research Hospital, Konya, Türkiye.
Fatma Arzu AkkuşDepartment of Internal Medicine, Division of Clinical Immunology and Allergy, Konya City Hospital, Konya, Türkiye.
Mehmet KılınçDepartment of Internal Medicine, Division of Clinical Immunology and Allergy, Batman Training and Research Hospital, Batman, Türkiye.
Selim KahramanDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University Faculty of Medicine, Akyokuş, Meram/Konya, 42080, Türkiye.
Şevket ArslanDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University Faculty of Medicine, Akyokuş, Meram/Konya, 42080, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlterations in immunoglobulin levels are commonly observed in hematologic malignancies and immune-mediated cytopenias, reflecting underlying immune dysregulation. While the prognostic relevance of hypogammaglobulinemia (HGG) has been studied in chronic lymphocytic leukemia (CLL), comparable data across a broader range of hematologic diagnoses remain limited. This study aimed to conduct a comparative analysis of baseline immunoglobulin profiles (IgG, IgA, IgM, IgE) across a heterogeneous cohort of patients with NHL, CLL, HL, ITP, and AIHA. Our primary objective was to evaluate the disease-specific associations of these profiles with survival outcomes to identify diagnostic groups that benefit most from baseline immune profiling.

resultsA total of 779 patients were included: 294 with NHL, 220 with CLL, 106 with HL, 128 with ITP, and 31 with AIHA. Quantitative and categorical analyses demonstrated significant differences in immunoglobulin levels across disease groups. CLL patients exhibited the highest frequency of low immunoglobulin levels, particularly for IgM and IgA. Kaplan–Meier analysis revealed numerically shorter overall survival in patients with low pretreatment IgG levels, although this difference was not statistically significant in the pooled heterogeneous cohort (p = 0.119). However, this association was not confirmed in the overall multivariable Cox regression model. Subgroup analysis using diagnosis-specific Cox models identified normal/high IgG status as independently associated with improved survival in NHL (HR: 0.543; p = 0.017), but not in CLL, HL, ITP, or AIHA. Associations for IgA, IgM, and IgE with mortality were not evaluated in these diagnosis-specific models.

conclusionsWhile low pretreatment IgG levels were associated with poorer survival in the overall cohort on univariate analysis, this association was not significant in the multivariable model. However, subgroup analysis identified low IgG as an independent and significant predictor of mortality in patients with NHL, but not in other diagnoses. These findings highlight that the prognostic value of immunoglobulin profiling is highly disease-specific. Baseline IgG assessment appears most relevant for risk stratification in NHL. However, the use of all-cause mortality limits our ability to discern the specific mechanism (e.g., infection-related vs. disease-progression-related) underlying this association.

Indexed as

Autoimmune DiseasesHematologic NeoplasmsImmunoglobulinsAdultAgedAged, 80 and overCohort StudiesCytopeniaFemaleHumansImmunoglobulin GKaplan-Meier EstimateMaleMiddle AgedPrognosisImmunoglobulin GImmunoglobulinsAutoimmune cytopeniasHematologic malignanciesHypogammaglobulinemiaImmune profilingImmunoglobulinsPrognosisSurvival analysis

Identifiers

PMID41673825
PMCPMC12997871

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Registered trials

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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.