Evidence map›Paper›PMID 41846912›Full record

ArticleFrontiers in immunology2026

Risk factors and surrogate indicators for cardiovascular disease are prevalent in Common Variable Immunodeficiency and associate with inflammatory phenotype.

Aidan Jia Sheng Yu, Fernando Moreira, Andrew Symes, Keegan Curlewis, Mary O'Sullivan, Joseph Jayasundera, Fatema-Zahra El Rhermoul, Charley Lever, Kostadin Stoenchev, Ke Li Chow and 12 more

Abstract read
In one paragraph

Article 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.

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0cells of the map it votes in
0citing papers in PubMed
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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

22 authors.

Aidan Jia Sheng YuDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Fernando MoreiraDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Andrew SymesDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Keegan CurlewisDepartment of Radiology, Royal Free Hospital London NHS Foundation Trust, London, United Kingdom.
Mary O'SullivanDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Joseph JayasunderaDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Fatema-Zahra El RhermoulDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Charley LeverDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Kostadin StoenchevDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Ke Li ChowDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Omer Faruk UysalUCL Respiratory, University College London, London, United Kingdom.
Ahmad M AlharbiUCL Respiratory, University College London, London, United Kingdom.
Sarita WorkmanDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Neil HallidaySheila Sherlock Liver Centre, Royal Free London NHS Foundation Trust, London, United Kingdom.
Arian LaurenceDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Nisha VermaDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Susan TadrosDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Sorena Kiani-AlikhanDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Joseph BarnettDepartment of Radiology, Royal Free Hospital London NHS Foundation Trust, London, United Kingdom.
Siobhan O BurnsDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
John R HurstUCL Respiratory, University College London, London, United Kingdom.
David M LoweDepartment of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Common variable immunodeficiency (CVID) is traditionally characterised by recurrent infections and immune dysregulation, but growing evidence suggests an increased risk of endothelial dysfunction and premature atherosclerosis in this population. Objective: To evaluate cardiovascular risk in patients with CVID through integration of clinical risk factors, biomarkers of endothelial dysfunction, and radiographic surrogates of subclinical atherosclerosis. Methods: A total of 101 CVID patients and 56 matched household controls were recruited. Data collected included cardiovascular risk factors, blood biomarkers (D-dimer, von Willebrand factor [vWF], fibrinogen, ESR, CRP), and immunological profiles. Existing imaging was reviewed, including thoracic CT for assessment of coronary artery calcification (CAC) and FibroScan for controlled attenuation parameter (CAP) scores; aortic pulse wave velocity (aPWV) was measured in a subset of participants. Subgroup analysis compared infection-only versus inflammatory/complex phenotypes of CVID. Results: CVID patients demonstrated high rates of hyperlipidaemia (38.6%), hypertension (23.8%), and diabetes/prediabetes (14.9%). CAC was present in 37%, with 82.4% having no known prior cardiovascular disease. Hepatic steatosis and elevated aPWV were observed in 30% and 6.5%, respectively. Patients with CAC were older and had higher rates of hypertension, diabetes, hyperlipidaemia, chronic kidney disease, elevated median vWF (227.5 vs 167 IU/dL, p=0.001), D-dimer (370.5 vs 271 ng/mL, p=0.011), and aPWV (8.2 vs 6.0 m/s, p=0.006). Patients with an inflammatory phenotype had higher vWF (224 vs 163 IU/dL, p<0.001) and D-dimer (314 vs 205 ng/mL, p=0.043) levels than those with infection-only CVID. Conclusion: CVID is associated with a substantial burden of cardiovascular risk factors and subclinical atherosclerosis, especially in the inflammatory phenotype.

Indexed as

Cardiovascular DiseasesCommon Variable ImmunodeficiencyInflammationAdultAgedBiomarkersFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedPhenotypePrevalenceRisk FactorsBiomarkersatherosclerosiscardiovascular riskcommon variable immunodeficiencycoronary artery calcificationd-dimerendothelial dysfunctioninflammatory phenotypevon Willebrand factor

Identifiers

PMID41846912
PMCPMC12989573

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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.