TY - JOUR
T1 - Evolution of Echocardiographic Measures of Cardiac Disease From CKD to ESRD and Risk of All-Cause Mortality
T2 - Findings From the CRIC Study
AU - CRIC Study Investigators
AU - Bansal, Nisha
AU - Roy, Jason
AU - Chen, Hsiang Yu
AU - Deo, Rajat
AU - Dobre, Mirela
AU - Fischer, Michael J.
AU - Foster, Elyse
AU - Go, Alan S.
AU - He, Jiang
AU - Keane, Martin G.
AU - Kusek, John W.
AU - Mohler, Emile
AU - Navaneethan, Sankar D.
AU - Rahman, Mahboob
AU - Hsu, Chi yuan
AU - Appel, Lawrence J.
AU - Feldman, Harold I.
AU - Go, Alan S.
AU - Kusek, John W.
AU - Lash, James P.
AU - Ojo, Akinlolu
AU - Rahman, Mahboob
AU - Townsend, Raymond R.
N1 - Funding Information:
Support: This work was supported by the following grants: K23 DK088865 (Dr Bansal), R01 DK70939 (Dr Hsu), and K24 DK92291 (Dr Hsu). Funding for the CRIC Study was obtained under a cooperative agreement from the National Institute of Diabetes and Digestive and Kidney Diseases (U01DK060990, U01DK060984, U01DK061022, U01DK061021, U01DK061028, U01DK060980, U01DK060963, and U01DK060902). This work was supported in part by the Perelman School of Medicine at the University of Pennsylvania Clinical and Translational Science Award (CTSA) National Institutes of Health (NIH)/National Center for Advancing Translational Sciences (NCATS) UL1TR000003 and K01 DK092353 (Dr Anderson), Johns Hopkins University UL1 TR-000424, University of Maryland General Clinical Research Center M01 RR-16500, Clinical and Translational Science Collaborative of Cleveland, UL1TR000439 from the NCATS component of the NIH and NIH Roadmap for Medical Research, Michigan Institute for Clinical and Health Research UL1TR000433, University of Illinois at Chicago CTSA UL1RR029879, Tulane COBRE for Clinical and Translational Research in Cardiometabolic Diseases P20 GM109036, Kaiser Permanente NIH/National Center for Research Resources UCSF-CTSI UL1 RR-024131. The funders did not have a role in study design; collection, analysis, and interpretation of the data; and writing of the manuscript.
Publisher Copyright:
© 2018 National Kidney Foundation, Inc.
PY - 2018/9
Y1 - 2018/9
N2 - Rationale & Objective: Abnormal cardiac structure and function are common in chronic kidney disease (CKD) and end-stage renal disease (ESRD) and linked with mortality and heart failure. We examined changes in echocardiographic measures during the transition from CKD to ESRD and their associations with post-ESRD mortality. Study Design: Prospective study. Setting & Participants: We studied 417 participants with CKD in the Chronic Renal Insufficiency Cohort (CRIC) who had research echocardiograms during CKD and ESRD. Predictor: We measured change in left ventricular mass index, left ventricular ejection fraction (LVEF), diastolic relaxation (normal, mildly abnormal, and moderately/severely abnormal), left ventricular end-systolic (LVESV), end-diastolic (LVEDV) volume, and left atrial volume from CKD to ESRD. Outcomes: All-cause mortality after dialysis therapy initiation. Analytical Approach: Cox proportional hazard models were used to test the association of change in each echocardiographic measure with postdialysis mortality. Results: Over a mean of 2.9 years between pre- and postdialysis echocardiograms, there was worsening of mean LVEF (52.5% to 48.6%; P < 0.001) and LVESV (18.6 to 20.2 mL/m2.7; P < 0.001). During this time, there was improvement in left ventricular mass index (60.4 to 58.4 g/m2.7; P = 0.005) and diastolic relaxation (11.11% to 4.94% with moderately/severely abnormal; P = 0.02). Changes in left atrial volume (4.09 to 4.15 mL/m2; P = 0.08) or LVEDV (38.6 to 38.4 mL/m2.7; P = 0.8) were not significant. Worsening from CKD to ESRD of LVEF (adjusted HR for every 1% decline in LVEF, 1.03; 95% CI, 1.00-1.06) and LVESV (adjusted HR for every 1 mL/m2.7 increase, 1.04; 95% CI, 1.02-1.07) were independently associated with greater risk for postdialysis mortality. Limitations: Some missing or technically inadequate echocardiograms. Conclusions: In a longitudinal study of patients with CKD who subsequently initiated dialysis therapy, LVEF and LVESV worsened and were significantly associated with greater risk for postdialysis mortality. There may be opportunities for intervention during this transition period to improve outcomes.
AB - Rationale & Objective: Abnormal cardiac structure and function are common in chronic kidney disease (CKD) and end-stage renal disease (ESRD) and linked with mortality and heart failure. We examined changes in echocardiographic measures during the transition from CKD to ESRD and their associations with post-ESRD mortality. Study Design: Prospective study. Setting & Participants: We studied 417 participants with CKD in the Chronic Renal Insufficiency Cohort (CRIC) who had research echocardiograms during CKD and ESRD. Predictor: We measured change in left ventricular mass index, left ventricular ejection fraction (LVEF), diastolic relaxation (normal, mildly abnormal, and moderately/severely abnormal), left ventricular end-systolic (LVESV), end-diastolic (LVEDV) volume, and left atrial volume from CKD to ESRD. Outcomes: All-cause mortality after dialysis therapy initiation. Analytical Approach: Cox proportional hazard models were used to test the association of change in each echocardiographic measure with postdialysis mortality. Results: Over a mean of 2.9 years between pre- and postdialysis echocardiograms, there was worsening of mean LVEF (52.5% to 48.6%; P < 0.001) and LVESV (18.6 to 20.2 mL/m2.7; P < 0.001). During this time, there was improvement in left ventricular mass index (60.4 to 58.4 g/m2.7; P = 0.005) and diastolic relaxation (11.11% to 4.94% with moderately/severely abnormal; P = 0.02). Changes in left atrial volume (4.09 to 4.15 mL/m2; P = 0.08) or LVEDV (38.6 to 38.4 mL/m2.7; P = 0.8) were not significant. Worsening from CKD to ESRD of LVEF (adjusted HR for every 1% decline in LVEF, 1.03; 95% CI, 1.00-1.06) and LVESV (adjusted HR for every 1 mL/m2.7 increase, 1.04; 95% CI, 1.02-1.07) were independently associated with greater risk for postdialysis mortality. Limitations: Some missing or technically inadequate echocardiograms. Conclusions: In a longitudinal study of patients with CKD who subsequently initiated dialysis therapy, LVEF and LVESV worsened and were significantly associated with greater risk for postdialysis mortality. There may be opportunities for intervention during this transition period to improve outcomes.
KW - CKD to ESRD transition
KW - Kidney
KW - all-cause mortality
KW - cardiac disease
KW - cardiovascular disease (CVD)
KW - dialysis
KW - dialysis initiation
KW - diastolic relaxation
KW - echocardiogram
KW - end-stage renal disease (ESRD)
KW - heart failure
KW - left atrial volume
KW - left ventricular ejection fraction (LVEF)
KW - left ventricular end-diastolic volume (LVEDV)
KW - left ventricular end-systolic volume (LVESV)
KW - left ventricular mass index (LVMI)
KW - subclinical CVD
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U2 - 10.1053/j.ajkd.2018.02.363
DO - 10.1053/j.ajkd.2018.02.363
M3 - Article
C2 - 29784617
AN - SCOPUS:85047180100
SN - 0272-6386
VL - 72
SP - 390
EP - 399
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 3
ER -