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Received on June 8, 2005
Accepted on August 16, 2005
Proteomics and Protein Markers |
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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