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Intestinal fatty acid binding protein is associated with coronary artery disease in long-term type 1 diabetes-the Dialong study.
- Source :
-
Cardiovascular diabetology [Cardiovasc Diabetol] 2024 Nov 19; Vol. 23 (1), pp. 419. Date of Electronic Publication: 2024 Nov 19. - Publication Year :
- 2024
-
Abstract
- Background: Individuals with type 1 diabetes are at increased risk of accelerated atherosclerosis, causing coronary artery disease (CAD). The underlying mechanisms remain unclear, but new theories proposed are damage of gut mucosa causing leakage and translocation of gut microbiota products into the circulation, leading to inflammatory responses and atherosclerosis. We therefore aimed to study the associations between gut related inflammatory biomarkers and coronary atherosclerosis in individuals with long-term type 1 diabetes.<br />Methods: In this cross-sectional, controlled study of 102 participants with type 1 diabetes and 63 control subjects, we measured circulating levels of intestinal fatty acid binding protein (I-FABP), soluble cluster of differentiation 14 (sCD14), lipopolysaccharide binding protein (LBP) and interleukin 18 (IL-18) by enzyme-linked immunosorbent assay (ELISA), and further gene expression of CD14 and toll-like receptor 4 (TLR4) by real time PCR in circulating leukocytes and peripheral blood mononuclear cells (PBMCs). The participants had either established coronary heart disease (CHD) or underwent computed tomography coronary angiography (CTCA) to assess for coronary atherosclerosis, including total, calcified and soft/mixed plaque volumes.<br />Results: In the diabetes group, the levels of I-FABP were significantly higher in participants with established CHD or significant stenosis on CTCA compared to the participants with normal arteries or non-significant stenosis, with median 1.67 ng/ml (interquartile range [IQR] 1.02-2.32) vs. median 1.09 ng/ml (IQR 0.82-1.58), p = 0.003. I-FABP was associated with significant coronary artery stenosis by CTCA (> 50%) or previously established CHD in the adjusted analysis (odds ratio [OR] = 2.32, 95% confidence interval [CI]: 1.09-4.95; p = 0.029). The levels of I-FABP correlated also to total coronary plaque volume (r = 0.22, p < 0.05). This association remained significant after adjusting for age, sex, persistent albuminuria, eGFR, statin treatment, diabetes duration and mean time-weighted variables; HbA1c, LDL-cholesterol and systolic blood pressure (OR = 1.97, 95% CI: 1.28-3.01; p = 0.002).<br />Conclusions: In this cohort of individuals with long-term type 1 diabetes I-FABP associated significantly with coronary artery stenosis, suggesting a potential role of gut mucosa damage in the process of atherosclerosis in type 1 diabetes.<br />Competing Interests: Declarations Ethics approval and consent to participate The study was approved by the regional ethics committee (project no. 2014/851). The study conformed to the Declaration of Helsinki. Consent for publication Not applicable. Competing interests The authors declare no competing interests.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Male
Female
Cross-Sectional Studies
Middle Aged
Case-Control Studies
Time Factors
Coronary Angiography
Adult
Toll-Like Receptor 4 blood
Toll-Like Receptor 4 genetics
Computed Tomography Angiography
Carrier Proteins blood
Carrier Proteins genetics
Membrane Glycoproteins blood
Inflammation Mediators blood
Plaque, Atherosclerotic
Risk Assessment
Risk Factors
Acute-Phase Proteins
Diabetes Mellitus, Type 1 blood
Diabetes Mellitus, Type 1 diagnosis
Diabetes Mellitus, Type 1 complications
Diabetes Mellitus, Type 1 epidemiology
Fatty Acid-Binding Proteins blood
Coronary Artery Disease blood
Coronary Artery Disease diagnostic imaging
Coronary Artery Disease epidemiology
Biomarkers blood
Lipopolysaccharide Receptors blood
Subjects
Details
- Language :
- English
- ISSN :
- 1475-2840
- Volume :
- 23
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cardiovascular diabetology
- Publication Type :
- Academic Journal
- Accession number :
- 39563343
- Full Text :
- https://doi.org/10.1186/s12933-024-02509-3