Evidence map›Paper›PMID 42707139›Full record

Observational studyFrontiers in immunology2026

Prevalence, associated clinical factors, and genetic characteristics of endocrinopathies in common variable immunodeficiency: a retrospective study of 95 adult patients from a single tertiary care center.

Ismail Yigitdol, Fatih Colkesen, Mehmet Emin Gerek, Ummugulsum Yilmaz Ergun, Secim Kolak, Emrah Harman, Ferhat Sagun, Sukran Aslan Savas, Sevket Arslan

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

9 authors.

Ismail YigitdolDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Fatih ColkesenDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Mehmet Emin GerekDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Ummugulsum Yilmaz ErgunDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Secim KolakDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Emrah HarmanDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Ferhat SagunDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Sukran Aslan SavasDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.
Sevket ArslanDivision of Clinical Immunology and Allergy, Department of Internal Medicine, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Common variable immunodeficiency (CVID) is the most common clinically significant primary antibody deficiency in adults, characterized by impaired immunoglobulin production and recurrent infections. Endocrinopathies represent a substantial burden in inborn errors of immunity, with reported prevalence rates of approximately 27-32.5%. Existing literature on CVID has focused mainly on autoimmune endocrinopathies, and no study has specifically evaluated endocrine disorders in adult CVID patients. This gap is clinically important because these patients may have non-autoimmune endocrinopathies as well as glucocorticoid -induced endocrinopathies due to long-term steroid therapy. We aimed to evaluate endocrinopathies in adult CVID patients and identify associated factors and genetic characteristics. Methods: This single-center retrospective observational study included 95 adult patients diagnosed with CVID who were followed at the Immunology and Allergy Diseases Clinic of Necmettin Erbakan University Faculty of Medicine between January 1, 2019, and December 31, 2025. The prevalence, associated clinical factors and generic characteristics of CVID patients with endocrinopathy were analyzed. Results: Among 95 CVID patients, 32(33.7%) had ≥1 endocrinopathy; 12 were glucocorticoid-induced. Patients with endocrinopathy had higher age, BMI, autoimmunity prevalence, prior glucocorticoid use, IgA levels, and switched memory B cells while bronchiectasis was more frequent in those without endocrinopathy. In multivariate logistic regression analysis, BMI, autoimmunity, and switched memory B-cell percentage were identified as independent predictors of endocrinopathy. Autoimmunity was the strongest predictor (OR: 12.812,95% CI:3.855-42.585). Among patients with endocrinopathies independent of glucocorticoid exposure, 5 patients had pathogenic/likely pathogenic variants, 1 likely benign, and 11 VUS; implicated genes included TNFRSF13B, IKZF1, ADA2 and MEFV. Conclusion: Endocrinopathies-including autoimmune, non-autoimmune, and glucocorticoid-induced disorders-represent a significant clinical burden in adult CVID patients. Larger multicenter studies are needed to further elucidate these complications.

Indexed as

Common Variable ImmunodeficiencyEndocrine System DiseasesAdultAgedFemaleGlucocorticoidsHumansMaleMiddle AgedPrevalenceRetrospective StudiesTertiary Care CentersYoung AdultGlucocorticoidsautoimmunitycommon variable immunodeficiency(CVID)endocrinopathygenetic variantglucocorticoid -induced

Identifiers

PMID42707139
PMCPMC13547094

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.