Increased sub-clinical coronary artery pathology in type 2 diabetes with albuminuria
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Increased sub-clinical coronary artery pathology in type 2 diabetes with albuminuria. / Rasmussen, Ida Kirstine Bull; Skriver-Moeller, Anne-Cathrine; Ripa, Rasmus Sejersten; Hasbak, Philip; Wasehuus, Victor Soendergaard; Hadji-Turdeghal, Katra; Zobel, Emilie Hein; Lassen, Martin Lyngby; Holmvang, Lene; Slomka, Piotr; Rossing, Peter; Kjaer, Andreas; Hansen, Tine Willum.
In: Diabetes, Vol. 73, No. 3, 2024, p. 490–496.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Increased sub-clinical coronary artery pathology in type 2 diabetes with albuminuria
AU - Rasmussen, Ida Kirstine Bull
AU - Skriver-Moeller, Anne-Cathrine
AU - Ripa, Rasmus Sejersten
AU - Hasbak, Philip
AU - Wasehuus, Victor Soendergaard
AU - Hadji-Turdeghal, Katra
AU - Zobel, Emilie Hein
AU - Lassen, Martin Lyngby
AU - Holmvang, Lene
AU - Slomka, Piotr
AU - Rossing, Peter
AU - Kjaer, Andreas
AU - Hansen, Tine Willum
N1 - © 2023 by the American Diabetes Association.
PY - 2024
Y1 - 2024
N2 - Diabetes affects the kidneys, and presence of albuminuria reflects widespread vascular damage and is a risk factor for cardiovascular disease (CVD). Still, the pathophysiological association between albuminuria and CVD remains incompletely understood. Recent advantages in non-invasive imaging enable functional assessment of coronary artery pathology and present an opportunity to explore the association between albuminuria and CVD. In this cross-sectional study, we evaluated the presence of sub-clinical coronary artery pathology in people with type 2 diabetes, free of overt CVD. Using multimodal imaging, we assessed the coronary microcalcification activity (18F-sodium fluoride positron emission tomography/computed tomography (PET/CT), plaque inflammation (64Cu- DOTATATE PET/CT) and myocardial flow reserve (82Rubidium PET/CT). The study population consisted of 90 participants, stratified by albuminuria; 60 had historic or current albuminuria (urine albumin creatinine ratio (UACR) ≥ 30 mg/g)), and 30 had normoalbuminuria (UACR < 30 mg/g). We demonstrated that any albuminuria (historic or current) was associated with a more severe phenotype, in particularly higher levels of microcalcifications and impaired myocardial microvascular function, however, coronary inflammation activity was similar in people with and without albuminuria. Our findings establish a potential underlying mechanism connecting cardiovascular and kidney diseases and could indicate the initial stages of the cardiorenal syndrome.
AB - Diabetes affects the kidneys, and presence of albuminuria reflects widespread vascular damage and is a risk factor for cardiovascular disease (CVD). Still, the pathophysiological association between albuminuria and CVD remains incompletely understood. Recent advantages in non-invasive imaging enable functional assessment of coronary artery pathology and present an opportunity to explore the association between albuminuria and CVD. In this cross-sectional study, we evaluated the presence of sub-clinical coronary artery pathology in people with type 2 diabetes, free of overt CVD. Using multimodal imaging, we assessed the coronary microcalcification activity (18F-sodium fluoride positron emission tomography/computed tomography (PET/CT), plaque inflammation (64Cu- DOTATATE PET/CT) and myocardial flow reserve (82Rubidium PET/CT). The study population consisted of 90 participants, stratified by albuminuria; 60 had historic or current albuminuria (urine albumin creatinine ratio (UACR) ≥ 30 mg/g)), and 30 had normoalbuminuria (UACR < 30 mg/g). We demonstrated that any albuminuria (historic or current) was associated with a more severe phenotype, in particularly higher levels of microcalcifications and impaired myocardial microvascular function, however, coronary inflammation activity was similar in people with and without albuminuria. Our findings establish a potential underlying mechanism connecting cardiovascular and kidney diseases and could indicate the initial stages of the cardiorenal syndrome.
U2 - 10.2337/db23-0529
DO - 10.2337/db23-0529
M3 - Journal article
C2 - 37992197
VL - 73
SP - 490
EP - 496
JO - Diabetes
JF - Diabetes
SN - 0012-1797
IS - 3
ER -
ID: 381061093