TY - JOUR
T1 - Association of cardiac valvular calcifications and C-reactive protein with cardiovascular mortality in incident hemodialysis patients
T2 - A Japanese cohort study
AU - Takahashi, Hiroshi
AU - Ishii, Hideki
AU - Aoyama, Toru
AU - Kamoi, Daisuke
AU - Kasuga, Hirotake
AU - Ito, Yasuhiko
AU - Yasuda, Kaoru
AU - Tanaka, Miho
AU - Yoshikawa, Daiji
AU - Maruyama, Shoichi
AU - Matsuo, Seiichi
AU - Murohara, Toyoaki
AU - Yuzawa, Yukio
PY - 2013/2
Y1 - 2013/2
N2 - Background: Cardiac valve calcification is seen frequently in patients undergoing dialysis. Serum C-reactive protein (CRP) level also is reported to predict future cardiovascular events. We investigated the association among valve calcification, CRP level, and mortality in patients with end-stage renal disease who were just beginning hemodialysis (HD) therapy. Study Design: Observational cohort. Setting & Participants: 1,290 consecutive patients who just started HD therapy were enrolled and were followed up to 10 years. Predictor: Patients were divided into 3 groups according to number of calcified valves: those without valve calcification, those with calcification in a single (aortic or mitral) valve, and those with calcification in both valves. They also were divided into tertiles according to CRP level. Outcomes: Cardiovascular and all-cause mortality. Measurements: Echocardiography and CRP measurement were performed within 1 month after beginning HD therapy. Results: During follow-up (median, 51 months), 335 (25.9%) patients died, including 156 (12.1%) of cardiovascular disease. The adjusted HR for cardiovascular mortality was 2.80 (95% CI, 1.63-4.81) for 2 calcifications versus 0 (P < 0.001). Furthermore, the risk of cardiovascular mortality was 3.66-fold higher in patients with calcifications in both valves (highest tertile of CRP) compared with patients without valve calcification (lowest tertile of CRP; P < 0.001). Limitations: Precise medical treatments or therapeutic interventions were not evaluated. Conclusions: Valve calcification and elevated CRP levels were not only related to additively increased risk of mortality, but also improved the prediction of mortality in patients with end-stage renal disease who had just begun HD therapy.
AB - Background: Cardiac valve calcification is seen frequently in patients undergoing dialysis. Serum C-reactive protein (CRP) level also is reported to predict future cardiovascular events. We investigated the association among valve calcification, CRP level, and mortality in patients with end-stage renal disease who were just beginning hemodialysis (HD) therapy. Study Design: Observational cohort. Setting & Participants: 1,290 consecutive patients who just started HD therapy were enrolled and were followed up to 10 years. Predictor: Patients were divided into 3 groups according to number of calcified valves: those without valve calcification, those with calcification in a single (aortic or mitral) valve, and those with calcification in both valves. They also were divided into tertiles according to CRP level. Outcomes: Cardiovascular and all-cause mortality. Measurements: Echocardiography and CRP measurement were performed within 1 month after beginning HD therapy. Results: During follow-up (median, 51 months), 335 (25.9%) patients died, including 156 (12.1%) of cardiovascular disease. The adjusted HR for cardiovascular mortality was 2.80 (95% CI, 1.63-4.81) for 2 calcifications versus 0 (P < 0.001). Furthermore, the risk of cardiovascular mortality was 3.66-fold higher in patients with calcifications in both valves (highest tertile of CRP) compared with patients without valve calcification (lowest tertile of CRP; P < 0.001). Limitations: Precise medical treatments or therapeutic interventions were not evaluated. Conclusions: Valve calcification and elevated CRP levels were not only related to additively increased risk of mortality, but also improved the prediction of mortality in patients with end-stage renal disease who had just begun HD therapy.
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U2 - 10.1053/j.ajkd.2012.09.007
DO - 10.1053/j.ajkd.2012.09.007
M3 - Article
C2 - 23122492
AN - SCOPUS:84872287337
SN - 0272-6386
VL - 61
SP - 254
EP - 261
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 2
ER -