03440nas a2200493 4500000000100000008004100001653001100042653001100053653000900064653000900073653001600082653001700098653001400115653003000129653001400159653002000173653001700193653002900210653005800239653002100297653004100318653002100359653003700380653002800417653006300445653002100508653003100529653003100560100001800591700001400609700001800623700001800641700001200659700001300671700001500684700001400699700001700713245015100730250001500881300001100896490000700907520198100914020005102895 2014 d10aFemale10aHumans10aAged10aMale10aMiddle Aged10aRisk Factors10aPrognosis10aPredictive Value of Tests10aIncidence10aRisk Assessment10aTime Factors10aBiological Markers/blood10aCardiovascular Diseases/ blood/diagnosis/epidemiology10aCystatin C/blood10aIntramolecular Oxidoreductases/blood10aLipocalins/blood10aNatriuretic Peptide, Brain/blood10aPeptide Fragments/blood10aRenal Insufficiency, Chronic/ blood/diagnosis/epidemiology10aTroponin T/blood10aUnited States/epidemiology10abeta 2-Microglobulin/blood1 aMatsushita K.1 aBallew S.1 aBallantyne C.1 aWoodward Mark1 aSang Y.1 aAstor B.1 aSolomon S.1 aCoresh J.1 aHoogeveen R.00aCardiac and kidney markers for cardiovascular prediction in individuals with chronic kidney disease: the Atherosclerosis Risk in Communities study a2014/05/31 a1770-70 v343 a

OBJECTIVE: Traditional predictors suboptimally predict cardiovascular disease (CVD) in individuals with chronic kidney disease (CKD). This study compared 5 nontraditional cardiac and kidney markers on the improvement of cardiovascular prediction among those with CKD. APPROACH AND RESULTS: Among 8622 participants aged 52 to 75 years in the Atherosclerosis Risk in Communities (ARIC) Study, cardiac troponin T, N-terminal pro-B-type natriuretic peptide, cystatin C, beta2-microglobulin, and beta-trace protein were compared for improvement in predicting incident CVD after stratifying by CKD status (940 participants with CKD [kidney dysfunction or albuminuria]). During a median follow-up of 11.9 years, there were 1672 CVD events including coronary disease, stroke, and heart failure (336 cases in CKD). Every marker was independently associated with incident CVD in participants with and without CKD. The adjusted hazard ratios (per 1 SD) were larger for cardiac markers than for kidney markers, particularly in CKD (1.61 [95% confidence interval, 1.43-1.81] for cardiac troponin T, 1.50 [1.34-1.68] for N-terminal pro-B-type natriuretic peptide, and <1.26 for kidney markers). Particularly in CKD group, cardiac markers compared with kidney markers contributed to greater c-statistic increment (0.032-0.036 versus 0.012-0.015 from 0.679 with only conventional predictors in CKD and 0.008-0.011 versus 0.002-0.010 from 0.697 in non-CKD) and categorical net reclassification improvement (0.086-0.127 versus 0.020-0.066 in CKD and 0.057-0.077 versus 0.014-0.048 in non-CKD). The superiority of cardiac markers was largely consistent in individual CVD outcomes. CONCLUSIONS: A greater improvement in cardiovascular prediction was observed for cardiac markers than for kidney markers in people with CKD. These results suggest that cardiac troponin T and N-terminal pro-B-type natriuretic peptide are useful for better CVD risk classification in this population.

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