TY - JOUR
T1 - Insights into Insulin Resistance and Calcification in the Myocardium in Type 2 Diabetes :
T2 - A Coronary Artery Analysis
AU - Simó Canonge, Rafael
AU - Aguadé-Bruix, Santiago
AU - Martín-Saladich, Queralt
AU - Simó-Servat, Olga
AU - Aparicio-Gómez, Carolina
AU - Hernández, Cristina
AU - Ramirez-Serra, Clara
AU - Pizzi, María Nazarena
AU - Roque, Albert
AU - González Ballester, Miguel A.
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/2/7
Y1 - 2023/2/7
N2 - Type 2 diabetes (T2D) is responsible for high incidence of cardiovascular (CV) complications leading to heart failure. Coronary artery region-specific metabolic and structural assessment could provide deeper insight into the extent of the disease and help prevent adverse cardiac events. Therefore, in this study, we aimed at investigating such myocardial dynamics for the first time in insulin-sensitive (mIS) and insulin-resistant (mIR) T2D patients. We targeted global and region-specific variations using insulin sensitivity (IS) and coronary artery calcifications (CACs) as CV risk factor in T2D patients. IS was computed using myocardial segmentation approaches at both baseline and after an hyperglycemic–insulinemic clamp (HEC) on [
18F]FDG-PET images using the standardized uptake value (SUV) (ΔSUV = SUV
HEC − SUV
BASELINE) and calcifications using CT Calcium Scoring. Results suggest that some communicating pathways between response to insulin and calcification are present in the myocardium, whilst differences between coronary arteries were only observed in the mIS cohort. Risk indicators were mostly observed for mIR and highly calcified subjects, which supports previously stated findings that exhibit a distinguished exposure depending on the impairment of response to insulin, while projecting added potential complications due to arterial obstruction. Moreover, a pattern relating calcification and T2D phenotypes was observed suggesting the avoidance of insulin treatment in mIS but its endorsement in mIR subjects. The right coronary artery displayed more ΔSUV, whilst plaque was more present in the circumflex. However, differences between phenotypes, and therefore CV risk, were associated to left descending artery (LAD) translating into higher CACs regarding IR, which could explain why insulin treatment was effective for LAD at the expense of higher likelihood of plaque accumulation. Personalized approaches to assess T2D may lead to more efficient treatments and risk-prevention strategies.
AB - Type 2 diabetes (T2D) is responsible for high incidence of cardiovascular (CV) complications leading to heart failure. Coronary artery region-specific metabolic and structural assessment could provide deeper insight into the extent of the disease and help prevent adverse cardiac events. Therefore, in this study, we aimed at investigating such myocardial dynamics for the first time in insulin-sensitive (mIS) and insulin-resistant (mIR) T2D patients. We targeted global and region-specific variations using insulin sensitivity (IS) and coronary artery calcifications (CACs) as CV risk factor in T2D patients. IS was computed using myocardial segmentation approaches at both baseline and after an hyperglycemic–insulinemic clamp (HEC) on [
18F]FDG-PET images using the standardized uptake value (SUV) (ΔSUV = SUV
HEC − SUV
BASELINE) and calcifications using CT Calcium Scoring. Results suggest that some communicating pathways between response to insulin and calcification are present in the myocardium, whilst differences between coronary arteries were only observed in the mIS cohort. Risk indicators were mostly observed for mIR and highly calcified subjects, which supports previously stated findings that exhibit a distinguished exposure depending on the impairment of response to insulin, while projecting added potential complications due to arterial obstruction. Moreover, a pattern relating calcification and T2D phenotypes was observed suggesting the avoidance of insulin treatment in mIS but its endorsement in mIR subjects. The right coronary artery displayed more ΔSUV, whilst plaque was more present in the circumflex. However, differences between phenotypes, and therefore CV risk, were associated to left descending artery (LAD) translating into higher CACs regarding IR, which could explain why insulin treatment was effective for LAD at the expense of higher likelihood of plaque accumulation. Personalized approaches to assess T2D may lead to more efficient treatments and risk-prevention strategies.
KW - Myocardium
KW - Insulin sensibility
KW - Type 2 diabetes
KW - [ 18 F]FDG-PET imaging
KW - Cardiovascular risk
KW - Coronary artery
KW - Metabolic disease
KW - Computed tomography
KW - Calcification
UR - http://www.scopus.com/inward/record.url?scp=85149031334&partnerID=8YFLogxK
U2 - 10.3390/ijms24043250
DO - 10.3390/ijms24043250
M3 - Article
C2 - 36834662
SN - 1422-0067
VL - 24
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 4
M1 - 3250
ER -