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Clinical Chemistry 0: clinchem.2005.055665v1, 2005; 10.1373/clinchem.2005.055665
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Received on June 8, 2005
Accepted on August 16, 2005

Proteomics and Protein Markers

Cardiac Troponins and Renal Function in Nondialysis Patients with Chronic Kidney Disease

Nasir A. Abbas 1, R. Ian John 1, Michelle C. Webb 1, Michelle E. Kempson 2, Aisling N. Potter 2, Christopher P. Price 3, Susan Vickery 2, Edmund J. Lamb 2*

1 Department of Renal Medicine, East Kent Hospitals NHS Trust, Canterbury, Kent, United Kingdom
2 Clinical Biochemistry, East Kent Hospitals NHS Trust, Canterbury, Kent, United Kingdom
3 Bayer Diagnostics plc, Newbury, Berkshire, United Kingdom

* To whom correspondence should be addressed. E-mail: edmund.lamb{at}ekht.nhs.uk.

Background: Serum cardiac troponin concentrations are commonly increased in end-stage renal disease (ESRD) in the absence of an acute coronary syndrome (ACS). The data on cardiac troponin I (cTnI) are more variable than those for cardiac troponin T (cTnT). There is little information on cardiac troponin concentrations in patients with chronic kidney disease (CKD) who have not commenced dialysis.

Methods: We studied 222 patients: 56 had progressed to stage 3 (moderate CKD); 70 to stage 4 (severe CKD); and 96 to stage 5 (kidney failure). Patients underwent echocardiography and were followed prospectively for a median of 19 months; all causes of mortality was recorded.

Results: Overall, serum cTnT was increased above the 99th percentile reference limit in 43% of all CKD patients studied, compared with 18% for cTnI. Serum cTnT and cTnI concentrations were more commonly increased in the presence of more severe CKD (11 and 6 patients in stage 3, 27 and 8 in stage 4, and 57 and 24 in stage 5 (P <0.0001 and <0.02, respectively). Among 38 patients with detectable cTnI, 32 had detectable cTnT (rs = 0.67; P<0.0001). There was evidence that decreasing estimated glomerular filtration rate (eGFR) increased the odds of having detectable cTnT (P <0.001) but not cTnI (P = 0.128). There was no evidence to support an adjusted association of detectable cardiac troponins with increasing left ventricular mass index. Increased cTnT (P = 0.0097), but not cTnI, was associated with decreased survival.

Conclusions: Increased cTnT and cTnI concentrations are relatively common in predialysis CKD patients, in the absence of an ACS, including among those with stage 3 disease. The presence of left ventricular hypertrophy alone does not explain these data. Detectable cTnT was a marker of decreased survival.




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