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Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
Published on: September 20, 2024
Risk factors and surrogate indicators for cardiovascular disease are prevalent in Common Variable Immunodeficiency
Aidan Jia Sheng Yu1, Fernando Moreira1, Andrew Symes1
1Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Insights
Common variable immunodeficiency (CVID) significantly increases cardiovascular risk, with high rates of atherosclerosis found even in patients without prior heart disease. The inflammatory CVID phenotype shows higher markers of endothelial dysfunction.
Area of Science:
- Immunology
- Cardiology
- Vascular Biology
Background:
- Common variable immunodeficiency (CVID) is linked to recurrent infections and immune dysregulation.
- Emerging evidence indicates an elevated risk of endothelial dysfunction and premature atherosclerosis in CVID patients.
Purpose of the Study:
- To assess cardiovascular risk in CVID patients.
- Integration of clinical risk factors, endothelial dysfunction biomarkers, and atherosclerosis surrogates.
- Evaluation of subclinical atherosclerosis in the CVID population.
Main Methods:
- Recruitment of 101 CVID patients and 56 matched controls.
- Collection of cardiovascular risk factors, blood biomarkers (D-dimer, vWF, fibrinogen, ESR, CRP), and immunological data.
- Review of imaging (CT for CAC, FibroScan for CAP) and measurement of aortic pulse wave velocity (aPWV).
Main Results:
- CVID patients exhibit high prevalence of hyperlipidemia, hypertension, and diabetes/prediabetes.
- 37% of CVID patients had coronary artery calcification (CAC), mostly without prior cardiovascular disease.
- Inflammatory CVID phenotypes showed elevated vWF and D-dimer levels compared to infection-only phenotypes.
Conclusions:
- Common variable immunodeficiency is associated with a significant burden of cardiovascular risk factors.
- Substantial subclinical atherosclerosis is present in CVID patients, particularly those with an inflammatory phenotype.
- These findings highlight the need for cardiovascular risk management in CVID.
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.
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