abstract
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Background
It is uncertain whether repeated measurements of a multi-target
biomarker panel may help to personalize medical heart failure (HF)
therapy to improve outcome in chronic HF.
Methods
This analysis included 499 patients from the Trial of Intensified
versus standard Medical therapy in Elderly patients with Congestive
Heart Failure (TIME-CHF), aged ≥ 60 years, LVEF
≤ 45%, and NYHA ≥ II, who had repeated clinical
visits within 19 months follow-up. The interaction between
repeated measurements of biomarkers and treatment effects of loop
diuretics, spironolactone, β-blockers, and renin-angiotensin
system (RAS) inhibitors on risk of HF hospitalization or death was
investigated in a hypothesis-generating analysis. Generalized
estimating equation (GEE) models were used to account for the
correlation between recurrences of events in a patient.
Results
One hundred patients (20%) had just one event (HF hospitalization or
death) and 87 (17.4%) had at least two events. Loop diuretic
up-titration had a beneficial effect for patients with high
interleukin-6 (IL6) or high high-sensitivity C-reactive protein
(hsCRP) (interaction, = 0.013 and
= 0.001), whereas the opposite was the case with low
hsCRP (interaction, = 0.013). Higher dosage of loop
diuretics was associated with poor outcome in patients with high
blood urea nitrogen (BUN) or prealbumin (interaction,
= 0.006 and = 0.001), but not in those
with low levels of these biomarkers. Spironolactone up-titration was
associated with lower risk of HF hospitalization or death in
patients with high cystatin C (CysC) (interaction,
= 0.021). β-Blockers up-titration might have a
beneficial effect in patients with low soluble fms-like tyrosine
kinase-1 (sFlt) (interaction, = 0.021). No treatment
biomarker interactions were found for RAS inhibition.
Conclusion
The data of this post hoc analysis suggest that decision-making
using repeated biomarker measurements may be very promising in
bringing treatment of heart failure to a new level in the context of
predictive, preventive, and personalized medicine. Clearly,
prospective testing is needed before this novel concept can be
adopted.
Clinical trial registration
isrctn.org, identifier: ISRCTN43596477.
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citation
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Davarzani N, Sanders-van Wijk S, Maeder M T, Rickenbacher P, Smirnov
E, Karel J, Suter T, De Boer R A, Block D, Rolny V, Zaugg C,
Pfisterer M E, Peeters R, Brunner-La Rocca H P, TIME-CHF
Investigators . Novel concept to guide systolic heart failure
medication by repeated biomarker testing-results from TIME-CHF in
context of predictive, preventive, and personalized medicine. EPMA J
2018; 9:161-173.
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