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Peer-reviewedCC BY-NC-NDCardiovascular diabetology

Associations between cardiac adipose tissue volume, measures of coronary calcification, myocardial microvascular function and systemic inflammation in individuals with type 2 diabetes free of overt cardiovascular disease.

6 more authors
13 affiliations
  1. 1Steno Diabetes Center Copenhagen, Borgmester Ib Juuls Vej 83, 2730, Herlev, Denmark.
  2. 2Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
  3. 3Department of Cardiology, Herlev & Gentofte Hospital, Hellerup, Denmark.
  4. 4Department of Internal Medicine 1, Holbæk Hospital, Holbæk, Denmark.
  5. 5Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  6. 6Department of Medicine, Zealand University Hospital, Nykøbing Falster, Denmark.
  7. 7Steno Diabetes Center Zealand, Zealand, Denmark.
  8. 8Department of Medicine, Zealand University Hospital, Køge, Denmark.
  9. 9Department of Cardiology, Rigshospitalet, Denmark.
  10. 10Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Bispebjerg, Copenhagen, Denmark.
  11. 11Cluster for Molecular Imaging, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  12. 12Steno Diabetes Center Copenhagen, Borgmester Ib Juuls Vej 83, 2730, Herlev, Denmark. [email protected].
  13. 13Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. [email protected].

Abstract

Background

Peri- and epicardial adipose tissue (PEAT) is a metabolically active fat depot surrounding the heart and coronary arteries that may contribute to vascular dysfunction and inflammation in type 2 diabetes (T2D). We examined associations between PEAT volume, coronary calcification (CACS), myocardial flow reserve (MFR), and systemic inflammation (hsCRP).Methods

Cross-sectional analysis of adults with T2D without overt CVD recruited 2020-2023. PEAT was quantified on non-contrast CT; CACS was calculated by the Agatston method; MFR was measured by rubidium-82 PET/CT; hsCRP assessed systemic inflammation. Associations were tested using multivariable regression adjusting for cardiovascular risk factors.Results

Among 887 participants (mean age 65 years; 70% male; mean BMI 30 kg/m²; median PEAT 199 mL [IQR 133-283]), higher PEAT (per 100 mL) was associated with lower MFR (β - 0.04; 95% CI - 0.09 to 0.00; p = 0.041) and higher hsCRP, corresponding to a 38% increase (95% CI 28% to 48%; p < 0.001) in age- and sex-adjusted models, but not with CACS > 300 (OR 1.01; 95% CI 0.89-1.15). After further adjustment for diabetes duration, BMI, LDL cholesterol, systolic blood pressure, HbA1c, kidney function, smoking, and albuminuria, only the association with hsCRP remained significant at 14% (95%; CI 4% to 25%; p = 0.005).Conclusion

In individuals with T2D without overt CVD, PEAT volume was not independently associated with CACS or MFR after multivariable adjustment. Higher PEAT volume was associated with higher hsCRP, suggesting a relationship with systemic inflammation; however, this exploratory finding should be interpreted in the context of established links between adiposity and inflammatory burden.

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BibTeX
@article{jensen2026associations,
  title = {{Associations between cardiac adipose tissue volume, measures of coronary calcification, myocardial microvascular function and systemic inflammation in individuals with type 2 diabetes free of overt cardiovascular disease.}},
  author = {Morten Steen Jensen and Ida K B Rasmussen and Anne-Cathrine Skriver-Møller and Philip Hasbak and Martin B Blond and Adam Chebli and Victor S Wasehuus and Mats C H Lassen and Morten Lindhardt and Allan Kofoed-Enevoldsen and Urd L Kielgast and Emilie H Zobel and Lene Holmvang and Tor Biering-Sørensen and Peter Rossing and Rasmus S Ripa and Andreas Kjaer and Tine W Hansen},
  journal = {Cardiovascular diabetology},
  year = {2026},
  month = jul,
  doi = {10.1186/s12933-026-03298-7},
  url = {https://europepmc.org/article/MED/42897624},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Associations between cardiac adipose tissue volume, measures of coronary calcification, myocardial microvascular function and systemic inflammation in individuals with type 2 diabetes free of overt cardiovascular disease.
AU  - Morten Steen Jensen
AU  - Ida K B Rasmussen
AU  - Anne-Cathrine Skriver-Møller
AU  - Philip Hasbak
AU  - Martin B Blond
AU  - Adam Chebli
AU  - Victor S Wasehuus
AU  - Mats C H Lassen
AU  - Morten Lindhardt
AU  - Allan Kofoed-Enevoldsen
AU  - Urd L Kielgast
AU  - Emilie H Zobel
AU  - Lene Holmvang
AU  - Tor Biering-Sørensen
AU  - Peter Rossing
AU  - Rasmus S Ripa
AU  - Andreas Kjaer
AU  - Tine W Hansen
PY  - 2026
DA  - 2026/07/01
JO  - Cardiovascular diabetology
DO  - 10.1186/s12933-026-03298-7
UR  - https://europepmc.org/article/MED/42897624
AB  - Background  Peri- and epicardial adipose tissue (PEAT) is a metabolically active fat depot surrounding the heart and coronary arteries that may contribute to vascular dysfunction and inflammation in type 2 diabetes (T2D). We examined associations between PEAT volume, coronary calcification (CACS), myocardial flow reserve (MFR), and systemic inflammation (hsCRP).Methods  Cross-sectional analysis of adults with T2D without overt CVD recruited 2020-2023. PEAT was quantified on non-contrast CT; CACS was calculated by the Agatston method; MFR was measured by rubidium-82 PET/CT; hsCRP assessed systemic inflammation. Associations were tested using multivariable regression adjusting for cardiovascular risk factors.Results  Among 887 participants (mean age 65 years; 70% male; mean BMI 30 kg/m²; median PEAT 199 mL [IQR 133-283]), higher PEAT (per 100 mL) was associated with lower MFR (β - 0.04; 95% CI - 0.09 to 0.00; p = 0.041) and higher hsCRP, corresponding to a 38% increase (95% CI 28% to 48%; p < 0.001) in age- and sex-adjusted models, but not with CACS > 300 (OR 1.01; 95% CI 0.89-1.15). After further adjustment for diabetes duration, BMI, LDL cholesterol, systolic blood pressure, HbA1c, kidney function, smoking, and albuminuria, only the association with hsCRP remained significant at 14% (95%; CI 4% to 25%; p = 0.005).Conclusion  In individuals with T2D without overt CVD, PEAT volume was not independently associated with CACS or MFR after multivariable adjustment. Higher PEAT volume was associated with higher hsCRP, suggesting a relationship with systemic inflammation; however, this exploratory finding should be interpreted in the context of established links between adiposity and inflammatory burden.
SN  - 1475-2840
ER  -