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Inflammatory bowel disease and cardiovascular risk: A meta-analysis
1Department of Gastroenterology, The First People's Hospital of Neijiang City, Sichuan, China.
Insights
Inflammatory bowel disease (IBD) significantly increases the risk of major adverse cardiovascular events (MACE), including heart attack and stroke. This risk is elevated in specific IBD subtypes, active disease, younger patients, and those with high glucocorticoid exposure.
Area of Science:
- Cardiovascular Health
- Gastroenterology
- Immunology
Background:
- Inflammatory bowel disease (IBD) is a chronic inflammatory condition.
- Emerging evidence links IBD to increased cardiovascular disease (CVD) risk.
- Major adverse cardiovascular events (MACE) occur earlier in IBD patients, independent of traditional risk factors.
Purpose of the Study:
- To systematically evaluate the association between IBD and MACE.
- To quantify the risk of myocardial infarction (MI), ischemic heart disease (IHD), and ischemic stroke in IBD patients.
- To explore risk variations based on IBD subtype, disease activity, and patient demographics.
Main Methods:
- Systematic literature search of Medline, Embase, and Cochrane Library (Jan 2015 - June 2025).
- Inclusion of original observational cohort and case-control studies with adjusted estimates.
- Meta-analysis using random effects models to pool data from 12 eligible studies (3,017,580 participants).
Main Results:
- IBD is significantly associated with increased risks of MI (HR=1.41), IHD (HR=1.37), and ischemic CVA (HR=1.28).
- Crohn's disease patients exhibited higher MI and IHD risks compared to ulcerative colitis.
- Active IBD, younger age (<40), and high cumulative glucocorticoid exposure independently elevated MACE risk.
Conclusions:
- IBD is an independent risk factor for MACE.
- Cardiovascular risk in IBD varies by disease subtype and activity.
- Glucocorticoid use is a significant contributor to MACE risk in IBD patients.
Background:
Inflammatory bowel disease (IBD) is a chronic immune-mediated intestinal disorder characterized by recurrent inflammation. Growing research over the last 10 years has connected IBD to heightened heart-related danger, with major adverse cardiovascular events (MACE, including myocardial infarction (MI), ischemic heart disease (IHD), ischemic stroke) arising earlier in life without reliance on conventional risk elements like high blood pressure or abnormal lipid levels.
Methods:
A systematic literature search was performed in Medline, Embase, and the Cochrane Library to identify observational cohort and case-control studies published from January 2015 through June 2025. Only original observational cohort and case-control studies with adjusted outcome estimates were enrolled; systematic reviews, meta-analyses, Mendelian randomization studies, and preclinical studies were strictly excluded. Two independent reviewers extracted data and assessed methodological quality using the Newcastle-Ottawa Scale. Meta-analysis was performed using random-effects models; forest plots were generated to visualize pooled effect estimates. Heterogeneity, sensitivity analyses, and publication bias were formally evaluated.
Results:
A total of 3126 records were retrieved, and finally 12 eligible original observational studies (10 cohort studies, 2 case-control studies) were included, involving 3,017,580 participants and 204,328 IBD cases. Pooled results showed that IBD was significantly associated with increased risks of MI (hazard ratio (HR) = 1.41, 95% confidence interval (95%CI): 1.30-1.53, I2 = 45%), IHD (HR = 1.37, 95%CI: 1.28-1.47, I2 = 53%), and ischemic cerebrovascular accident (CVA; HR = 1.28, 95%CI: 1.19-1.38, I2 = 40%). Subgroup analysis indicated Crohn's disease had higher MI and IHD risks than ulcerative colitis; active IBD and patients under 40 years also presented significantly elevated MACE risk. Additional subgroup analysis confirmed that high cumulative glucocorticoid exposure was independently associated with increased MACE risk (HR/relative risk = 1.52, 95%CI: 1.31-1.76, p < 0.001).
Conclusions:
This meta-analysis confirms that IBD is independently associated with increased risk of MACE (MI, IHD, and ischemic CVA), with differential risks by subtype, disease activity, and age.
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