TY - JOUR
T1 - Cholesterol efflux capacity of high-density lipoprotein correlates with survival and allograft vasculopathy in cardiac transplant recipients
AU - Javaheri, Ali
AU - Molina, Maria
AU - Zamani, Payman
AU - Rodrigues, Amrith
AU - Novak, Eric
AU - Chambers, Susan
AU - Stutman, Patricia
AU - Maslanek, Wilhelmina
AU - Williams, Mary
AU - Lilly, Scott M.
AU - Heeger, Peter
AU - Sayegh, Mohamed H.
AU - Chandraker, Anil
AU - Briscoe, David M.
AU - Daly, Kevin P.
AU - Starling, Randall
AU - Ikle, David
AU - Christie, Jason
AU - Rame, J. Eduardo
AU - Goldberg, Lee R.
AU - Billheimer, Jeffrey
AU - Rader, Daniel J.
N1 - Publisher Copyright:
© 2016 International Society for Heart and Lung Transplantation
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Background Cardiac allograft vasculopathy (CAV) is a major cause of mortality after cardiac transplantation. High-density lipoprotein (HDL) cholesterol efflux capacity (CEC) is inversely associated with coronary artery disease. In 2 independent studies, we tested the hypothesis that reduced CEC is associated with mortality and disease progression in CAV. Methods We tested the relationship between CEC and survival in a cohort of patients with CAV (n = 35). To determine whether reduced CEC is associated with CAV progression, we utilized samples from the Clinical Trials in Organ Transplantation 05 (CTOT05) study to determine the association between CEC and CAV progression and status at 1 year (n = 81), as assessed by average change in maximal intimal thickness (MIT) on intravascular ultrasound. Results Multivariable Cox proportional hazard models demonstrated that higher levels of CEC were associated with improved survival (hazard ratio 0.26, 95% confidence interval 0.11 to 0.63) per standard deviation CEC, p = 0.002). Patients who developed CAV had reduced CEC at baseline and 1-year post-transplant. We observed a significant association between pre-transplant CEC and the average change in MIT, particularly among patients who developed CAV at 1 year (β = −0.59, p = 0.02, R2 = 0.35). Conclusion Reduced CEC is associated with disease progression and mortality in CAV patients. These findings suggest the hypothesis that interventions to increase CEC may be useful in cardiac transplant patients for prevention or treatment of CAV.
AB - Background Cardiac allograft vasculopathy (CAV) is a major cause of mortality after cardiac transplantation. High-density lipoprotein (HDL) cholesterol efflux capacity (CEC) is inversely associated with coronary artery disease. In 2 independent studies, we tested the hypothesis that reduced CEC is associated with mortality and disease progression in CAV. Methods We tested the relationship between CEC and survival in a cohort of patients with CAV (n = 35). To determine whether reduced CEC is associated with CAV progression, we utilized samples from the Clinical Trials in Organ Transplantation 05 (CTOT05) study to determine the association between CEC and CAV progression and status at 1 year (n = 81), as assessed by average change in maximal intimal thickness (MIT) on intravascular ultrasound. Results Multivariable Cox proportional hazard models demonstrated that higher levels of CEC were associated with improved survival (hazard ratio 0.26, 95% confidence interval 0.11 to 0.63) per standard deviation CEC, p = 0.002). Patients who developed CAV had reduced CEC at baseline and 1-year post-transplant. We observed a significant association between pre-transplant CEC and the average change in MIT, particularly among patients who developed CAV at 1 year (β = −0.59, p = 0.02, R2 = 0.35). Conclusion Reduced CEC is associated with disease progression and mortality in CAV patients. These findings suggest the hypothesis that interventions to increase CEC may be useful in cardiac transplant patients for prevention or treatment of CAV.
KW - cardiac allograft vasculopathy
KW - cholesterol efflux capacity
KW - high-density lipoprotein
KW - survival
KW - transplantation
UR - http://www.scopus.com/inward/record.url?scp=84994424532&partnerID=8YFLogxK
U2 - 10.1016/j.healun.2016.06.022
DO - 10.1016/j.healun.2016.06.022
M3 - Article
C2 - 27498384
AN - SCOPUS:84994424532
SN - 1053-2498
VL - 35
SP - 1295
EP - 1302
JO - Journal of Heart and Lung Transplantation
JF - Journal of Heart and Lung Transplantation
IS - 11
ER -