Abstract: FR-OR97
Increased Coronary Artery Pathology in Type 2 Diabetes Without Cardiovascular Disease but with Albuminuria
Session Information
- Novel Clinical Impacts on Cardiorenal Disease
November 03, 2023 | Location: Room 103, Pennsylvania Convention Center
Abstract Time: 05:24 PM - 05:33 PM
Category: Hypertension and CVD
- 1602 Hypertension and CVD: Clinical
Authors
- Hansen, Tine, Steno Diabetes Center Copenhagen, Herlev, Capital Region, Denmark
- Rasmussen, Ida, Steno Diabetes Center Copenhagen, Herlev, Capital Region, Denmark
- Skriver-Møller, Anne-Cathrine, Steno Diabetes Center Copenhagen, Herlev, Capital Region, Denmark
- Ripa, Rasmus S., Department of Clinical Physiology & Nuclear Medicine, Copenhagen, Denmark
- Hasbak, Philip, Department of Clinical Physiology & Nuclear Medicine, Copenhagen, Denmark
- Wasehuus, Victor, Steno Diabetes Center Copenhagen, Herlev, Capital Region, Denmark
- Hadji-Turdeghal, Katra, Rigshospitalet, Kobenhavn, Denmark
- Zobel, Emilie, Steno Diabetes Center Copenhagen, Herlev, Capital Region, Denmark
- Lassen, Martin Lyngby, Department of Clinical Physiology & Nuclear Medicine, Copenhagen, Denmark
- Slomka, Piotr, Departments of Medicine and Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, United States
- Rossing, Peter, Steno Diabetes Center Copenhagen, Herlev, Denmark
- Kjaer, Andreas, Department of Clinical Physiology & Nuclear Medicine, Copenhagen, Denmark
Background
Advances in non-invasive imaging enables combined structural and functional assessment of coronary artery pathophysiology. We evaluated sub-clinical coronary artery pathology using multimodal imaging in persons with type 2 diabetes.
Methods
Cross-sectional study including persons with type 2 diabetes, without known cardiovascular disease or symptoms. Coronary microcalcification activity was measured using 18F-sodium fluoride positron emission tomography/computed tomography (PET/CT). Plaque inflammation was measured using 64Cu-DOTATATE PET/CT and estimated as coronary inflammation activity. Myocardial flow reserve was calculated using 82Rubidium PET/CT, and the coronary artery calcium score was quantified using CT.
Results
We included 90 participants, 30 had normoalbuminuria (urine albumin creatinine ratio (UACR) <30 mg/g) and 60 had current albuminuria or a history of albuminuria (UACR ≥ 30 mg/g). Mean age was 65 (SD 7.5) years, 19 % were females. Participants with albuminuria had increased microcalcification activity (median 0.75 [IQR: 0.30 -1.85]) compared to normoalbuminuria (0.43 [0.24 - 0.87]; p=0.04), but not after adjustment for clinical risk factors for cardiovascular disease (p=0.09). Microcalcification activity was positively associated with the current level of UACR (standardized β=0.53, p=0.008), and a trend remained after adjustment (β=0.44, p=0.05). Mean myocardial flow reserve was lower in participants with albuminuria (2.5 (SD 0.7)) compared to normoalbuminuria (2.9 (0.7); p=0.02), but not after adjustment (p=0.07). Coronary inflammation activity and coronary artery calcium score were similar between albuminuria groups (p≥0.40). Higher current level of UACR was associated with lower myocardial flow reserve (β=-0.42, p=0.03) and higher coronary artery calcium score (β=0.40, p=0.03) in unadjusted analysis. Current level of UACR was not associated with coronary inflammation activity (p=0.74).
Conclusion
In persons with type 2 diabetes, without cardiovascular disease, the presence of albuminuria was associated with sub-clinical coronary artery pathology and microcalcifications when compared to normoalbuminuria.
Funding
- Private Foundation Support