In:
European Journal of Heart Failure, Wiley, Vol. 19, No. 3 ( 2017-03), p. 357-365
Abstract:
Biomarkers can be used for diagnosis, risk stratification, or management of patients with heart failure ( HF ). Knowledge about the biological variation is needed for proper interpretation of serial measurements. Therefore, we aimed to determine and compare the biological variation of a large panel of biomarkers in healthy subjects and in patients with chronic HF . Methods and results The biological variability of established biomarkers [ NT‐proBNP and high‐sensitivity troponin T ( hsTnT )], novel biomarkers [galectin‐3, suppression of tumorigenicity 2 ( ST2 ), and growth differentiation factor 15 ( GDF ‐15)], and renal/neurohormonal biomarkers (aldosterone, phosphate, parathyroid hormone, plasma renin concentration, and creatinine) was determined in 28 healthy subjects and 83 HF patients, over a period of 4 months and 6 weeks, respectively. The analytical ( CV a ), intraindividual ( CV i ), and interindividual ( CV g ) variations were calculated, as well as the reference change value ( RCV ), which reflects the percentage of change that may indicate a ‘relevant’ change. All crude biomarker levels were significantly increased or decreased in HF patients compared with controls (all P 〈 0.01). Variation indices were comparable in healthy individuals and HF patients. CV i was not influenced by the individual levels of the biomarker itself. NT‐proBNP and GDF ‐15 had relatively high CV i (21.8% and 16.6%) and RCV (61.7% and 64.3%), whereas ST2 ( CV i , 15.0; RCV , 42.9%), hsTnT ( CV i , 11.1; RCV , 31.4%), and galectin‐3 ( CV i , 8.1; RCV , 25.0%) had lower indices of variation. Conclusion Biological variation indices are comparable between healthy subjects and HF patients for a broad spectrum of biomarkers. NT‐proBNP and GDF ‐15 have substantial variation, with lower variation for ST2 , hsTnT , and galectin‐3. These data are instrumental in proper interpretation of biomarker levels in HF patients.
Type of Medium:
Online Resource
ISSN:
1388-9842
,
1879-0844
DOI:
10.1002/ejhf.2017.19.issue-3
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
1500332-2
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