Hemodialysis and biomarkers of myocardial infarction – a cohort study

Author:

Hasselbalch Rasmus Bo12,Alaour Bashir3,Kristensen Jonas Henrik12,Couch Liam S.3,Kaier Thomas E.3,Nielsen Ture Lange1,Plesner Louis Lind1,Strandkjær Nina12,Schou Morten14,Rydahl Casper5,Goetze Jens P.6,Bundgaard Henning47,Marber Michael3,Iversen Kasper Karmark124

Affiliation:

1. Department of Cardiology , Copenhagen University Hospital – Herlev and Gentofte Hospital , Copenhagen , Denmark

2. Department of Emergency Medicine , Copenhagen University Hospital – Herlev and Gentofte Hospital , Copenhagen , Denmark

3. King’s College London British Heart Foundation Centre , Rayne Institute, St Thomas’ Hospital , London , UK

4. Department of Clinical Medicine , University of Copenhagen , Copenhagen , Denmark

5. Department of Nephrology , Copenhagen University Hospital – Herlev and Gentofte Hospital , Copenhagen , Denmark

6. Department of Clinical Biochemistry , Copenhagen University Hospital – Rigshospitalet , Copenhagen , Denmark

7. Department of Cardiology , Copenhagen University Hospital – Rigshospitalet , Copenhagen , Denmark

Abstract

Abstract Objectives End-stage renal disease is associated with a high risk of cardiovascular disease. We compared the concentration and prognostic ability of high sensitivity cardiac troponin T (hs-cTnT) and I (hs-cTnI) and cardiac myosin-binding protein C (cMyC) among stable hemodialysis patients. Methods Patients were sampled before and after hemodialysis. We measured hs-cTnI, hs-cTnT and cMyC and used Cox regressions to assess the association between quartiles of concentrations and all-cause mortality and a combination of cardiovascular events and all-cause mortality during follow-up. Results A total of 307 patients were included, 204 males, mean age 66 years (SD 14). Before dialysis, 299 (99 %) had a hs-cTnT concentration above the 99th percentile, compared to 188 (66 %) for cMyC and 35 (11 %) for hs-cTnI. Hs-cTnT (23 %, p<0.001) and hs-cTnI (15 %, p=0.049) but not cMyC (4 %, p=0.256) decreased during dialysis. Follow-up was a median of 924 days (492–957 days); patients in the 3rd and 4th quartiles of hs-cTnT (3rd:HR 3.0, 95 % CI 1.5–5.8, 4th:5.2, 2.7–9.8) and the 4th quartile of hs-cTnI (HR 3.8, 2.2–6.8) had an increased risk of mortality. Both were associated with an increased risk of the combined endpoint for patients in the 3rd and 4th quartiles. cMyC concentrations were not associated with risk of mortality or cardiovascular event. Conclusions Hs-cTnT was above the 99th percentile in almost all patients. This was less frequent for hs-cTnI and cMyC. High cTn levels were associated with a 3-5-fold higher mortality. This association was not present for cMyC. These findings are important for management of hemodialysis patients.

Funder

Herlev Hospital

Candys Foundation

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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