TY - JOUR
T1 - Association of cardiovascular risk factors on myocardial perfusion and fibrosis in asymptomatic individuals
T2 - cardiac magnetic resonance study
AU - Cha, Min Jae
AU - Kim, Sung Mok
AU - Kim, Hyun Su
AU - Kim, Yiseul
AU - Choe, Yeon Hyeon
N1 - Publisher Copyright:
© The Foundation Acta Radiologica 2018.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - Background: Myocardial perfusion reserve index (MPRI) and extracellular volume fraction (ECV) on cardiac magnetic resonance (CMR) are known to quantify coronary microvascular dysfunction and myocardial fibrosis, respectively. Purpose: To demonstrate that cardiovascular risk factors such as hypertension, diabetes, hyperlipidemia, and smoking are correlated with MPRI and ECV on CMR in asymptomatic individuals. Material and Methods: Between October 2013 and July 2014, 196 individuals underwent CMR. After excluding those with chest pain, arrhythmia, and obstructive coronary artery disease, participants were divided into five groups: those without risk factor (n = 26) and those with one (n = 43), two (n = 35), three (n = 24), or four (n = 6) risk factors. MPRI and ECV were obtained on perfusion CMR and pre- and post-T1 mapping, respectively. Results: A total of 134 asymptomatic individuals (109 men, 25 women; mean age = 54.4 ± 7.08 years; body mass index [BMI] = 24.96 ± 2.76 kg/m2; Framingham risk score [FRS] = 7.71 ± 5.21) were included. The Jonckheere-Terpstra test demonstrated trends of increasing BMI, FRS, and left ventricular mass index (all P values < 0.001), but decreasing MPRI (P = 0.001) with increasing numbers of risk factors. Stepwise multiple linear regression demonstrated that an increasing number of cardiovascular risk factors was an independent predictor of MPRI (P = 0.001). However, there was no significant association between the number of risk factors and ECV (P = 0.99). Conclusion: We demonstrated that an increasing number of cardiovascular risk factors is significantly associated with reduced MPRI, but not with ECV on CMR.
AB - Background: Myocardial perfusion reserve index (MPRI) and extracellular volume fraction (ECV) on cardiac magnetic resonance (CMR) are known to quantify coronary microvascular dysfunction and myocardial fibrosis, respectively. Purpose: To demonstrate that cardiovascular risk factors such as hypertension, diabetes, hyperlipidemia, and smoking are correlated with MPRI and ECV on CMR in asymptomatic individuals. Material and Methods: Between October 2013 and July 2014, 196 individuals underwent CMR. After excluding those with chest pain, arrhythmia, and obstructive coronary artery disease, participants were divided into five groups: those without risk factor (n = 26) and those with one (n = 43), two (n = 35), three (n = 24), or four (n = 6) risk factors. MPRI and ECV were obtained on perfusion CMR and pre- and post-T1 mapping, respectively. Results: A total of 134 asymptomatic individuals (109 men, 25 women; mean age = 54.4 ± 7.08 years; body mass index [BMI] = 24.96 ± 2.76 kg/m2; Framingham risk score [FRS] = 7.71 ± 5.21) were included. The Jonckheere-Terpstra test demonstrated trends of increasing BMI, FRS, and left ventricular mass index (all P values < 0.001), but decreasing MPRI (P = 0.001) with increasing numbers of risk factors. Stepwise multiple linear regression demonstrated that an increasing number of cardiovascular risk factors was an independent predictor of MPRI (P = 0.001). However, there was no significant association between the number of risk factors and ECV (P = 0.99). Conclusion: We demonstrated that an increasing number of cardiovascular risk factors is significantly associated with reduced MPRI, but not with ECV on CMR.
KW - asymptomatic
KW - Cardiac magnetic resonance
KW - cardiovascular risk factor
KW - extracellular volume fraction
KW - myocardial perfusion reserve index
UR - https://www.scopus.com/pages/publications/85044260116
U2 - 10.1177/0284185118757274
DO - 10.1177/0284185118757274
M3 - Article
C2 - 29433344
AN - SCOPUS:85044260116
SN - 0284-1851
VL - 59
SP - 1300
EP - 1308
JO - Acta Radiologica
JF - Acta Radiologica
IS - 11
ER -