Cardiovascular Complications Are Increased in Inflammatory Bowel Disease: A Path Toward Achievement of a Personalized Risk Estimation

<b>Background/Objectives</b>: The global burden of inflammatory bowel diseases (IBDs) continues to rise, with up to 50% of patients experiencing extraintestinal manifestations. Cardiovascular diseases (CVDs) are of particular concern, ranking as the second leading cause of mortality in this population. Despite a comparatively lower prevalence of traditional cardiovascular (CV) risk factors, the persistent inflammatory milieu and immune dysregulation inherent to IBD may contribute to heightened CVD risk. In this study, following a review of the current literature, an ongoing prospective trial designed to clarify CV risk profiles in IBD patients is detailed. <b>Methods</b>: A cohort of patients with IBD is being enrolled for comprehensive baseline evaluation of CV risk factors, lifestyle metrics, and disease characteristics. The incidence of major adverse cardiovascular events (MACEs) will be tracked and contrasted with a gender- and age-matched non-IBD cohort over a 2-year follow-up period. In cases of MACE occurrence, a multi-omics analysis-including genomic, proteomic, transcriptomic, and microbiome profiling-will be performed, along with a parallel evaluation in matched IBD controls without MACE. An artificial intelligence (AI) framework will support the analysis of this complex dataset. <b>Results</b>: To date, over 150 patients with IBD have been enrolled, and detailed phenotypic data and biological samples have been collected. <b>Conclusions</b>: We aim to introduce an IBD-specific correction factor for existing CV risk scores upon study completion. This is particularly relevant for individuals under 40 years of age, who are often inadequately assessed by current risk stratification models.

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Publication Details

Journal
Journal of Personalized Medicine
Published
2025-09-02
DOI
https://doi.org/10.3390/jpm15090418
Citations
3
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
5.45
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article

Cardiovascular Complications Are Increased in Inflammatory Bowel Disease: A Path Toward Achievement of a Personalized Risk Estimation

Paolo Biamonte, Vito Annese, Giuseppe Dell’Anna, Guglielmo Albertini Petroni et al.
3 citations
Journal of Personalized Medicine
Inflammatory Bowel Disease
5.45
article

Cardiovascular Complications Are Increased in Inflammatory Bowel Disease: A Path Toward Achievement of a Personalized Risk Estimation

Paolo Biamonte, Vito Annese, Giuseppe Dell’Anna, Guglielmo Albertini Petroni, Serenella Castelvecchio, Anna Latiano, Maria Laura Annunziata, Sofia Cinque, M. Parisi, Emanuele Orlando
article en
3 citations

Abstract

<b>Background/Objectives</b>: The global burden of inflammatory bowel diseases (IBDs) continues to rise, with up to 50% of patients experiencing extraintestinal manifestations. Cardiovascular diseases (CVDs) are of particular concern, ranking as the second leading cause of mortality in this population. Despite a comparatively lower prevalence of traditional cardiovascular (CV) risk factors, the persistent inflammatory milieu and immune dysregulation inherent to IBD may contribute to heightened CVD risk. In this study, following a review of the current literature, an ongoing prospective trial designed to clarify CV risk profiles in IBD patients is detailed. <b>Methods</b>: A cohort of patients with IBD is being enrolled for comprehensive baseline evaluation of CV risk factors, lifestyle metrics, and disease characteristics. The incidence of major adverse cardiovascular events (MACEs) will be tracked and contrasted with a gender- and age-matched non-IBD cohort over a 2-year follow-up period. In cases of MACE occurrence, a multi-omics analysis-including genomic, proteomic, transcriptomic, and microbiome profiling-will be performed, along with a parallel evaluation in matched IBD controls without MACE. An artificial intelligence (AI) framework will support the analysis of this complex dataset. <b>Results</b>: To date, over 150 patients with IBD have been enrolled, and detailed phenotypic data and biological samples have been collected. <b>Conclusions</b>: We aim to introduce an IBD-specific correction factor for existing CV risk scores upon study completion. This is particularly relevant for individuals under 40 years of age, who are often inadequately assessed by current risk stratification models.

Journal of Personalized MedicineVol. 15(9)
Vita-Salute San Raffaele University (IT), University of Pavia (IT), Casa Sollievo della Sofferenza (IT), IRCCS Policlinico San Donato (IT), Federico II University Hospital (IT)
Openalex Percentile: Top 4%
Inflammatory Bowel Disease
5.45
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