Evidence map›Paper›PMID 40928712›Full record

ReviewCurrent atherosclerosis reports2025

From Gut Inflammation to Cardiovascular Conflagration: Mapping IBD's Cardiometabolic Risks.

Oscar Noble, Dayoung Jeon, Megan Lewis, Christopher Fan, Khurram Nasir, Bincy P Abraham

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current atherosclerosis reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

6 authors.

Oscar NobleDivision of Gastroenterology and Hepatology, Lynda K. and David M. Underwood Center for Digestive Health, Houston Methodist Hospital, Houston, TX, USA.ORCID http://orcid.org/0000-0002-9842-8712
Dayoung JeonDivision of Gastroenterology and Hepatology, Lynda K. and David M. Underwood Center for Digestive Health, Houston Methodist Hospital, Houston, TX, USA.ORCID http://orcid.org/0000-0003-2045-0159
Megan LewisDivision of Gastroenterology and Hepatology, Lynda K. and David M. Underwood Center for Digestive Health, Houston Methodist Hospital, Houston, TX, USA.ORCID http://orcid.org/0009-0006-1753-4043
Christopher FanDivision of Gastroenterology and Hepatology, Lynda K. and David M. Underwood Center for Digestive Health, Houston Methodist Hospital, Houston, TX, USA.ORCID http://orcid.org/0000-0002-7117-6885
Khurram NasirWeill Cornell Medical College, Cornell University, New York City, NY, USA.ORCID http://orcid.org/0000-0001-5376-2269
Bincy P AbrahamDivision of Gastroenterology and Hepatology, Lynda K. and David M. Underwood Center for Digestive Health, Houston Methodist Hospital, Houston, TX, USA. bpabraham@houstonmethodist.org.ORCID http://orcid.org/0000-0003-0308-1224

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis review aims to characterize the known cardiovascular (CV) manifestations associated with inflammatory bowel disease (IBD) and the underlying mechanisms driving these associations. RECENT

findingsGut dysbiosis, a hallmark of patients with IBD, can result in both local and systemic inflammation, thereby potentially increasing the risk of cardiovascular disease (CVD) in the IBD population. Micronutrient deficiencies, anemia, and sarcopenia independently increase the risk of CVD and are frequent comorbidities of patients with IBD. IBD is a chronic inflammatory condition with significant and underrecognized cardiovascular complications. Patients with IBD frequently develop coronary artery disease (CAD) in the absence of traditional risk factors such as obesity and smoking and experience an earlier onset of CVD compared to the general population. Moreover, IBD has been associated with increased risks of arrhythmia, myocarditis, pericarditis, heart failure, and venous thromboembolism. Nontraditional risk factors related to IBD, including disease activity, prolonged disease duration, and cardiovascular risks associated with certain IBD medications, significantly contribute to the increased risk of CVD. While additional prospective research is required to fully elucidate the mechanisms driving CVD in IBD patients, current evidence suggests that minimizing disease activity, optimizing nutritional status, addressing gut dysbiosis, and mitigating the traditional risk factors could significantly reduce the burden of CVD in the IBD population. As our understanding of the link between IBD and cardiovascular disease grows, healthcare providers must closely monitor cardiovascular health and risk factors in patients with IBD, particularly during flares, active disease, and hospitalizations.

Indexed as

Cardiovascular DiseasesInflammationInflammatory Bowel DiseasesDysbiosisGastrointestinal MicrobiomeHeart Disease Risk FactorsHumansRisk FactorsCardiovascular diseaseInflammationInflammatory bowel diseaseMicrobiome

Identifiers

PMID40928712

What Socratic 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 Socratic graph.