TY - JOUR
T1 - Cinacalcet, fibroblast growth factor-23, and cardiovascular disease in hemodialysis
T2 - The evaluation of cinacalcet HCl therapy to lower cardiovascular events (EVOLVE) trial
AU - Evaluation of Cinacalcet HCL Therapy to Lower Cardiovascular Events (EVOLVE) Trial Investigators
AU - Moe, Sharon M.
AU - Chertow, Glenn M.
AU - Parfrey, Patrick S.
AU - Kubo, Yumi
AU - Block, Geoffrey A.
AU - Correa-Rotter, Ricardo
AU - Drüeke, Tilman B.
AU - Herzog, Charles A.
AU - London, Gerard M.
AU - Mahaffey, Kenneth W.
AU - Wheeler, David C.
AU - Stolina, Maria
AU - Dehmel, Bastian
AU - Goodman, William G.
AU - Floege, Jürgen
AU - Santos, J.
AU - Najun Zarazaga, C.
AU - Marin, I.
AU - Garrote, N.
AU - Cusumano, A.
AU - Peñalba, N.
AU - Del Valle, E.
AU - Juncos, L.
AU - Martinez Saye, J.
AU - Lef, L.
AU - Altobelli, V.
AU - Petraglia, G.
AU - Rosa Diez, G.
AU - Douthat, W.
AU - Lobo, J.
AU - Gallart, C.
AU - Lafalla, A.
AU - Diez, G.
AU - Linares, B.
AU - Lopez, N.
AU - Ramirez, N.
AU - Gonzalez, R.
AU - Valtuille, R.
AU - Beresan, H.
AU - Hermida, O.
AU - Rudolf, G.
AU - Marchetta, N.
AU - Rano, M.
AU - Ramirez, M.
AU - García, N.
AU - Gillies, A.
AU - Jones, B.
AU - Pedagogos, E.
AU - Walker, R.
AU - Renders, L.
N1 - Publisher Copyright:
© 2015 American Heart Association, Inc.
PY - 2015
Y1 - 2015
N2 - Background. Patients with kidney disease have disordered bone and mineral metabolism, including elevated serum concentrations of fibroblast growth factor-23 (FGF23). These elevated concentrations are associated with cardiovascular and all-cause mortality. The objective was to determine the effects of the calcimimetic cinacalcet (versus placebo) on reducing serum FGF23 and whether changes in FGF23 are associated with death and cardiovascular events. Methods and Results. This was a secondary analysis of a randomized clinical trial comparing cinacalcet to placebo in addition to conventional therapy (phosphate binders/vitamin D) in patients receiving hemodialysis with secondary hyperparathyroidism (intact parathyroid hormone .300 pg/mL). The primary study end point was time to death or a first nonfatal cardiovascular event (myocardial infarction, hospitalization for angina, heart failure, or a peripheral vascular event). This analysis included 2985 patients (77% of randomized) with serum samples at baseline and 2602 patients (67%) with samples at both baseline and week 20. The results demonstrated that a significantly larger proportion of patients randomized to cinacalcet had .30% (68% versus 28%) reductions in FGF23. Among patients randomized to cinacalcet, a .30% reduction in FGF23 between baseline and week 20 was associated with a nominally significant reduction in the primary composite end point (relative hazard, 0.82; 95% confidence interval, 0.69.0.98), cardiovascular mortality (relative hazard, 0.66; 95% confidence interval, 0.50.0.87), sudden cardiac death (relative hazard, 0.57; 95% confidence interval, 0.37.0.86), and heart failure (relative hazard, 0.69; 95% confidence interval, 0.48.0.99). Conclusions. Treatment with cinacalcet significantly lowers serum FGF23. Treatment-induced reductions in serum FGF23 are associated with lower rates of cardiovascular death and major cardiovascular events.
AB - Background. Patients with kidney disease have disordered bone and mineral metabolism, including elevated serum concentrations of fibroblast growth factor-23 (FGF23). These elevated concentrations are associated with cardiovascular and all-cause mortality. The objective was to determine the effects of the calcimimetic cinacalcet (versus placebo) on reducing serum FGF23 and whether changes in FGF23 are associated with death and cardiovascular events. Methods and Results. This was a secondary analysis of a randomized clinical trial comparing cinacalcet to placebo in addition to conventional therapy (phosphate binders/vitamin D) in patients receiving hemodialysis with secondary hyperparathyroidism (intact parathyroid hormone .300 pg/mL). The primary study end point was time to death or a first nonfatal cardiovascular event (myocardial infarction, hospitalization for angina, heart failure, or a peripheral vascular event). This analysis included 2985 patients (77% of randomized) with serum samples at baseline and 2602 patients (67%) with samples at both baseline and week 20. The results demonstrated that a significantly larger proportion of patients randomized to cinacalcet had .30% (68% versus 28%) reductions in FGF23. Among patients randomized to cinacalcet, a .30% reduction in FGF23 between baseline and week 20 was associated with a nominally significant reduction in the primary composite end point (relative hazard, 0.82; 95% confidence interval, 0.69.0.98), cardiovascular mortality (relative hazard, 0.66; 95% confidence interval, 0.50.0.87), sudden cardiac death (relative hazard, 0.57; 95% confidence interval, 0.37.0.86), and heart failure (relative hazard, 0.69; 95% confidence interval, 0.48.0.99). Conclusions. Treatment with cinacalcet significantly lowers serum FGF23. Treatment-induced reductions in serum FGF23 are associated with lower rates of cardiovascular death and major cardiovascular events.
KW - arrhythmias, cardiac
KW - calcium
KW - death, sudden, cardiac
KW - renal insufficiency, chronic
KW - ventricular remodeling
UR - http://www.scopus.com/inward/record.url?scp=84935451711&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.114.013876
DO - 10.1161/CIRCULATIONAHA.114.013876
M3 - Article
C2 - 26059012
AN - SCOPUS:84935451711
SN - 0009-7322
VL - 132
SP - 27
EP - 39
JO - Circulation
JF - Circulation
IS - 1
ER -