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[-tj_pname-]Critical CareThis Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon.Fi
broblast growth factor 23 in acute myocardial infarction complicated by cardiogenic shock: a biomarker substudy of the intra-aortic balloon pump in cardiogenic shock II (IABP-SHOCK II) trialCritical Care
doi:10.-014-0713-8Georg Fuernau (georg.fuernau@medizin.uni-leipzig.de) Janine P?ss (janine.poess@uksh.de) Daniel Denks (denks.) Steffen Desch (steffen.desch@uksh.de) Gunnar H Heine (gunnar.heine@uks.eu) Ingo Eitel (ingo.eitel@gmx.de) Sarah Seiler (sarah.seiler@uks.eu) Suzanne de Waha (s-) Sebastian Ewen (sebastian.ewen@uks.eu) Andreas Link (andreas.link@uks.eu) Gerhard Schuler (gerhard.schuler@medizin.uni-leipzig.de) Volker Adams (volker.adams@medizin.uni-leipzig.de) Michael B?hm (michael.boehm@uks.de) Holger Thiele (holger.thiele@uksh.de)SampleISSN Article type Submission date Acceptance date Article URL Research 5 September 2014 8 December 2014 /content/18/6/713Like all articles in BMC journals, this peer-reviewed article can be downloaded, printed and distributed freely for any purposes (see copyright notice below). Articles in BMC journals are listed in PubMed and archived at PubMed Central. For information about publishing your research in BMC journals or any BioMed Central journal, go to /info/authors/? Fuernau et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.Fibroblast growth factor 23 in acute myocardial infarction complicated by cardiogenic shock: a biomarker substudy of the intra-aortic balloon pump in cardiogenic shock II (IABP-SHOCK II) trialGeorg Fuernau1*,? * Corresponding author Email: georg.fuernau@medizin.uni-leipzig.de Janine P?ss2,3,? Email: janine.poess@uksh.de Daniel Denks1 Email: denks. Steffen Desch1,2 Email: steffen.desch@uksh.de Gunnar H Heine4 Email: gunnar.heine@uks.eu Ingo Eitel1,2 Email: ingo.eitel@gmx.de Sarah Seiler4 Email: sarah.seiler@uks.eu Suzanne de Waha1,5 Email: s- Sebastian Ewen3 Email: sebastian.ewen@uks.eu Andreas Link3 Email: andreas.link@uks.eu Gerhard Schuler1 Email: gerhard.schuler@medizin.uni-leipzig.de Volker Adams1 Email: volker.adams@medizin.uni-leipzig.de Michael B?hm3 Email: michael.boehm@uks.deHolger Thiele1,2 Email: holger.thiele@uksh.de1Clinic for Internal Medicine/Cardiology, University of Leipzig C Heart Center, Strümpellstra?e 39, 04289 Leipzig, Germany2Medical Clinic II, Universit?tsklinikum Schleswig-Holstein (UKSH), Campus Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany3Department of Internal Medicine III - Cardiology, Angiology, and Intensive Care Medicine, Saarland University Medical Center and Saarland University Faculty of Medicine, Kirrberger Stra?e 100, 66421 Homburg, Germany4Internal Medicine IV - Nephrology and Hypertension, Clinic for Internal Medicine IV - Nephrology and Hypertension, Saarland University Medical Center and Saarland University Faculty of Medicine, Kirrberger Stra?e 100, 66421 Homburg, Germany5Department of Cardiology, Heart Center Segeberger Kliniken GmbH, Am Kurpark 1, 23795 Bad Segeberg, Germany?Equal contributors.AbstractIntroductionCardiogenic shock (CS) is the leading cause of death in patients hospitalized with acute myocardial infarction (AMI). Biomarkers might help in risk stratification and understanding of pathophysiology. Preliminary data suggests that patients with CS face a profound increase in the osteocyte-derived hormone fibroblast growth factor 23 (FGF-23), which acts as a negative regulator of serum phosphate levels. The present study aimed to assess the predictive role of FGF-23 for clinical outcome in a large cohort of CS patients with and without renal dysfunction.MethodsIn the randomized intra-aortic balloon pump in cardiogenic shock II (IABP-SHOCK II)-trial, 600 patients with CS complicating AMI were assigned to therapy with or without IABP. Our predefined biomarker substudy included 182 patients. Blood sampling was performed in a standardized procedure at three different time points (day 1 (day of admission), day 2 and day 3). Differences in outcome of patients with FGF-23 levels & and & median were compared by log-rank-testing. Stepwise logistic regression modeling was performed to identify predictors of death at 30 days and Cox-regression analysis for time to death during the first year.ResultsAt all three time points, non-survivors had significantly higher FGF-23 levels compared to survivors (P &0.001 for all). Patients with FGF-23 levels above the median (395 RU/mL[interquartile range 102;2395]) were characterized by an increased 30-day mortality and 1year mortality. In multivariable analysis FGF-23 levels remained independent predictors for 30-day (odds ratio per 10log 1.80, 95% confidence interval [CI] 1.11 to 2.92; P = 0.02) and 1-year mortality (hazard ratio 1.50, 95% CI 1.11 to 2.04, P = 0.009). After stratifying the patients according to their baseline serum creatinine levels, the negative prognostic association of increased FGF-23 was only significant in those with serum creatinine greater than median.ConclusionIn CS, high levels of FGF-23 are independently related to a poor clinical outcome. However, this prognostic association appears only to apply in patients with impaired renal function.Trial registrationClinicalTrials.gov Identifier: NCT. Registered 22 June 2007.IntroductionCardiogenic shock (CS) represents the leading cause of death in patients hospitalized with acute myocardial infarction (AMI) [1-3]. Despite advances in treatment over the last decades, mortality rates are still approaching 50%. The pathophysiology of CS is characterized by an activation of neurohormones and inflammatory markers, which contribute to a vicious spiral resulting in systemic inflammatory response syndrome and finally leading to death [4]. Epidemiologic studies indicate that hyperphosphatemia is related to cardiovascular morbidity and mortality. This relationship has first been observed in patients with chronic kidney disease (CKD), but interestingly, it was found also in the general population [5]. Fibroblast growth factor 23 (FGF-23) is a phosphaturic hormone produced by osteocytes [6]. It acts by reducing phosphate absorption in the intestinal tract, increasing renal phosphate excretion, and lowering renal vitamin D activation [7]. Furthermore, FGF-23 seems to be up-regulated due to activation of the renin-angiotensin-aldosterone-system [8] which may explain the high levels of FGF-23 observed in CS [9]. Serum levels of FGF-23 have been shown to predict cardiovascular events in patients with CKD [10,11], in patients with normal renal function and a prevalent cardiovascular disease [12] and also among individuals from the general population [13,14]. Very recent evidence suggests that, within the broad spectrum of cardiovascular diseases, FGF-23 might be a much stronger predictor of incident heart failure events rather than of atherosclerotic vascular events, both among CKD patients, [10,11] and among subjects with a preserved renal function [15]. This close association between FGF-23 and myocardial disease was further confirmed in two recent cohort studies that selectively recruited patients with stable chronic systolic heart failure, among whom FGF-23 independently predicted cardiovascular events and total mortality [12,13]. In line, several clinical studies associated FGF-23 with markers of myocardial damage, namely left ventricular hypertrophy [16-18] and left ventricular dysfunction [19]. However, it is still controversial whether these associations are causal and whether FGF-23 exerts direct effects on the cardiovascular system [16,20].A prior small study found that in patients with AMI complicated by CS without apparent preexisting CKD FGF-23 levels were profoundly increased, showing more than 10 fold higher FGF-23 levels in patients with CS compared to patients with stable coronary artery disease. Furthermore, increased FGF-23 concentrations were associated with worse clinical outcome [9]. Notably, FGF-23 levels in patients with uncomplicated AMI did not differ from those of stable CAD patients [9]. This observed increase in CS patients exceeded by far the one observed in patients with hyperphosphatemia due to CKD and thus, seemed to occur largely (if not completely) independently of the serum phosphate levels of the patients and suggests that C at least under certain circumstances C CS may induce elevated FGF-23 levels. Limitations of this preliminary study were its small sample size with low numbers of events and that the prognostic role of FGF-23 was not assessed with regard to renal function. The present study aimed to further assess the prognostic association of FGF-23 in a larger, better characterized population with infarction-related CS included in a prospective, randomized clinical trial and to investigate its relationship to renal function.MethodsPatients and study designThe present study is a predefined substudy of the Intraaortic Balloon Pump (IABP) in Cardiogenic Shock II-trial (IABP-SHOCK II; ClinicalTrials.gov Identifier: NCT) comparing the use of IABP versus no IABP support in patients with CS complicating AMI. This study did not show a significant difference between the two groups with respect to short and long-term outcome. The design of the trial and its main results have been published previously [21-23]. In brief, 600 patients were enrolled in 37 centers in Germany and were randomized to either IABP support or to control in a 1:1 fashion. CS was defined as hypotension, pulmonary congestion, and signs of end-organ hypoperfusion. Exclusion criteria were duration of CS &12 hours, cardiopulmonary resuscitation &30 minutes, severe cerebral deficit, mechanical causes of CS, age &90 years, absolute contraindications against IABP insertion, shock of other cause, or severe concomitant disease with life expectancy &6 months. Of the 600 patients included in the trial, 218 were enrolled at the University of Leipzig - Heart Center with a prospectively planned serial blood sampling. From 182 of these patients, blood samples were available for the present analysis (Figure 1). All patients underwent cardiac catheterization immediately after hospital admission. In resuscitated patients, cooling was initiated after PCI and blood sampling. The study was conducted according to the Declaration of Helsinki, has been approved by the ethical board of the medical faculty at the University of L K?the-Kollwitz-Stra?e 82, 04109 Leipzig and all patients or their legal representatives gave written informed consent. Figure 1 Study flow. FGF-23 = fibroblast growth factor-23.Laboratory measurementsBlood samples were collected under standardized conditions at different, predefined timepoints (day 1 [day of admission during primary PCI], day 2 and day 3). Samples were immediately centrifuged at 2,400 g for 10 minutes at room temperature. Supernatants were stored in aliquots at -80° C until further use. C-terminal FGF-23 was measured from EDTAplasma samples by enzyme-linked immunosorbent assay (FGF-23: Immunotopics, SanClemente, CA, USA; low cut-off value 3 rU/mL, high cut-off value 2000 rU/mL. Samples with FGF-23 & 2000 rU/mL were measured after dilution). Samples were assayed in duplicate. Plasma levels of creatinine, serum lactate and troponin T were measured by standard institutional laboratory measurements. For assessment of the association of FGF-23 levels with outcome with respect to renal function, the patient cohort was divided by the median of baseline serum creatinine.Statistical analysisCategorical data are presented as counts or proportions with the corresponding percentages and compared by Chi2 C test. Most continuous variables were not normally distributed. For reasons of uniformity, summary statistics for all continuous variables are thus presented as medians with interquartile range (IQR). For comparison of continuous variables, student’s ttest or Mann-Whitney test were used, as appropriate. Spearman’s-rank-correlation was used to investigate associations between continuous variables. For outcome analysis, all-cause mortality at 30 days and 1 year was used. Patients were stratified into two groups according to the median of FGF-23 concentrations at baseline. Log-rank-testing was used for outcome assessment. Stepwise logistic regression modeling for short-term (30-day) mortality and Coxregression modeling for long-term (1-year) mortality were performed. All baseline variables with an association (p-value &0.1) to short- or long-term mortality in univariable analysis entered the specific model. To assess the association between kidney function and increased FGF-23 levels at baseline (& vs. &median), patients were stratified in two groups according to the median of serum creatinine concentrations at baseline and the odds ratios were assessed separately including the calculation for interaction. Finally, the diagnostic accuracy of FGF23 for the prediction of mortality was explored by receiver-operating-characteristics-curve analysis. Comparison of the area under the curves (AUC) of FGF-23, serum lactate and a combination of both factors by multivariable logistic regression was performed with cstatistics. Statistical analysis was performed using commercially available software (MedCalc for Windows, version 13.3.1.0; MedCalc Software, Ostend, Belgium). A two-tailed p-value &0.05 was considered statistically significant.ResultsThe baseline characteristics of patients with FGF-23 concentrations at baseline below and above the median (median: 395 RU/mL, IQR 102;2395) are depicted in Table 1. As compared to patients & median, those with FGF-23 & median were older, had worse renal function, higher serum lactate and troponin concentrations. In addition, they were more likely to be female, to have prevalent peripheral artery disease, and / or coronary triple vessel disease. Of the 182 CS patients, 73 (40.1%) died within 30 days and 97 (53.3%) within one year.Table 1 Baseline characteristicsOverall FGF-23 & median FGF-23 & median p-value n = 182 n = 91 n = 91 Age (years) 71 (58;79) 67 (54;75) 74 (63;81) &0.001 Male sex, n (%) 126 (69) 71 (78) 55 (60) 0.02 Body mass index (kg/m2) 27.3 (24.5;29.4) 27.5 (24.7;29.7) 27.1 (24.5;29.4) 0.49 Baseline serum creatinine (μmol/L) 117 (95;163) 99 (81;123) 147 (109;208) &0.001 Baseline serum lactate (mmol/L) 3.7 (2.3;7.1) 3.0 (2.0;5.5) 4.6 (3.1;7.8) &0.001 Baseline troponin T (μg/L) 0.9 (0.3;2.9) 0.7 (0.2;1.6) 1.2 (0.4;3.4) 0.01 Heart rate at admission (n/min) 91 (75;110) 90 (72;110) 98 (78;114) 0.16 Systolic blood pressure at admission (mmHg) 86 (78;106) 85 (79;105) 86 (78;106) 0.98 Hypertension, n (%) 127 (70) 57 (63) 70 (77) 0.053 Hypercholesterolemia, n (%) 55 (30) 22 (24) 33 (36) 0.11 Diabetes mellitus, n (%) 65 (36) 28 (31) 37 (41) 0.22 Known peripheral artery disease, n (%) 22 (12) 5 (5) 17 (19) 0.01 Prior myocardial infarction, n (%) 39 (21) 20 (22) 19 (21) 0.99 Prior PCI, n (%) 33 (18) 17 (19) 16 (18) 0.99 Prior CABG, n (%) 10 (6) 6 (7) 4 (4) 0.75 Randomized to IABP, n (%) 89 (49) 51 (56) 38 (42) 0.08 Triple vessel disease, n (%) 90 (50) 33 (36) 57 (63) &0.001 Resuscitation, n (%) 67 (37) 38 (42) 29 (32) 0.22 Mechanical ventilation at admission, n (%) 95 (52) 45 (49) 50 (55) 0.55 FGF-23 = fibroblast growth factor-23; PCI = percutaneous c CABG = coronary IABP = intra-aortic balloon pump.Association of FGF-23 with clinical outcomeNon-survivors after 30 days had significantly higher FGF-23 levels c this difference was even more accentuated at day 2 and day 3 (Figure 2). In Kaplan-Meier analysis, patients with baseline FGF-23 levels above the median were characterized by an increased 30-day and 1 year mortality (Figure 3A). A landmark analysis in the 30 day survivors showed that a mortality difference was also found after the acute phase (Figure 3B). Also FGF-23 levels on day 2 and 3 were predictive in Kaplan-Meier-analysis for short-term (Day 2: hazard ratio [HR] 2.41, 95% confidence interval [CI] 1.29 C 4.49, p = 0.007, Day 3: HR 2.89, 95%CI 1.56 C 5.34, p = 0.001), and long-term mortality (Day 2: HR 2.31, 95%CI 1.41 C 3.80, p = 0.001, Day 3: HR 3.13, 95%CI 1.91 C 5.14, p & 0.001). Figure 2 Levels of FGF-23 on the different time points for 30 day-survivors and nonsurvivors. FGF-23 = fibroblast growth factor-23. Figure 3 A + B: Kaplan-Meier curves for patients with FGF-23 levels & median (red dashed line) and & median (blue line) for the overall cohort (A) and as landmark analysis for patients surviving until day 30 (B). FGF-23 = fibroblast growth factor-23; HR = CI = confidence interval.Regression analysisIn univariable logistic regression analysis FGF-23, age, EF, serum lactate and serum creatinine concentrations showed an association with time to 30-day mortality (p & 0.1 for all). In multivariable stepwise logistic regression analysis including these parameters, FGF-23 concentration remained an independent predictor of clinical outcome at 30 days (Table 2). Inlong-term (1 year) survival analysis including the same parameters, FGF-23 levels also remained independent predictors for time to death (independent predictors: FGF-23 per 10LOG: HR 1.50, 95%CI 1.11 C 2.04, p = 0.009, age per 10 years: HR 1.27, 95%CI 1.03 C 1.56, p = 0.03; ejection fraction per 10% increase: HR 0.76, 95%CI 0.62 C 0.92, p = 0.006; serum lactate per 10LOG: HR 2.92, 95%CI 1.23 C 6.94, p = 0.009, coronary 3-vessel disease and baseline serum creatinine, both univariable predictive, were not significant in multivariable testing). Table 2 Multivariable stepwise logistic regression analysis for 30-day mortalityUnivariable analysis OR 95%CI P FGF-23 per 10LOG 2.08 1.41 C 3.06 &0.001 Age per 10 years 1.30 1.02 - 1.66 0.03 Ejection fraction per 10% 0.59 0.44 C 0.80 &0.001 Diabetes mellitus 1.21 0.65 C 2.24 0.54 Serum lactate per 10LOG 7.90 2.79 C 22.42 &0.001 4.18 Serum creatinine per 10LOG 15.35 2.92 C 80.77 0.001 Troponin T per 10LOG 1.29 0.80 C 2.07 0.30 Known peripheral artery disease 1.28 0.52 C 3.15 0.59 Systolic blood pressure per 10 mmHg 0.93 0.81 C 1.08 0.33 Randomized to control group 1.13 0.62 C 2.04 0.69 Female gender 1.46 0.77 C 2.76 0.25 3-vessel disease 1.57 0.86 C 2.85 0.14 Resuscitation prior randomization 1.36 0.74 C 2.50 0.33 Mechanical ventilation at admission. 1.43 0.79 C 2.60 0.24 OR = CI = FGF -23 = fibroblast growth factor-23. Multivariable stepwise logistic regression analysis OR 95%CI P 1.80 1.11 C 2.92 0.02 0.63 0.46 C 0.86 0.003 1.17 C 14.87 0.03 -Receiver operating characteristicsIn c-statistics, the AUC of FGF-23 levels was equal to the one of serum lactate concentrations at baseline with regard to the prediction of 30-day mortality (FGF-23 vs. serum lactate: 0.677 vs. 0.673; p = 0.95). Interestingly, when combining both factors, the AUC increased significantly compared to the AUC of serum lactate alone (0.724 vs. 0.673; p = 0.04).FGF-23 and renal functionBaseline FGF-23 levels correlated moderately with baseline serum creatinine levels (r = 0.583; p & 0.001). Patients were stratified in two groups according to the median creatinine levels at baseline (117 μmol/L). FGF-23 levels at baseline were significantly higher in patients with serum creatinine levels & median (low vs. high creatinine: 150 [IQR 69; 485] vs. ; 5706] RU/mL, p & 0.001). The difference in FGF-23 concentrations between survivors and non-survivors was only evident in the group of patients with creatinine concentrations above the median (FGF-23: 626 [IQR 164;3673] versus 86] RU/mL, p & 0.001), whereas in the group with creatinine concentrations below the median, no differences in FGF-23 levels were observed with respect to the survival of the patients (141 (72;458) versus 204 (62;524) RU/mL, p = 0.72). In accordance, the negative prognostic association of increased baseline FGF-23 with 30-day mortality as well as 1-year mortality was only significant in patients with serum creatinine above the median, whereas in the group of patients with creatinine below the median, no difference was observed (Figure 4A + B). This was also observed for the adjusted HR for long-term mortality by quartiles of FGF-23concentration (Table 3). The calculated interaction terms for baseline FGF-23 & and & median with baseline serum creatinine & and & median in prediction of short- (p = 0.04) and longterm (p = 0.01) survival were significant (Figure 5). When the population was divided into tertiles by baseline serum creatinine the AUC for the prognostic value in ROC analysis of baseline FGF-23 increased per tertile (Group 1 [creatinine ≤ 100 μmol/L]: AUC 0.515; Group 2 [creatinine 101-142 μmol/L]: AUC 0.675; Group 3 [creatinine ≥ 142 μmol/L]: AUC 0.750). Figure 4 A + B: Kaplan-Meier curves for patients with FGF-23 levels & median (red dashed line) and & median (blue line) for patients with baseline serum creatinine & median (A) and & median (B). FGF-23 = fibroblast growth factor-23; HR = CI = confidence interval. Table 3 Fibroblast growth factor-23 quartiles and hazard ratios with 95% confidence interval for long-term mortality adjusted for age, ejection fraction and baseline serum lactateOverall cohort Creatinine ≥117 μmol/L Creatinine &117 μmol/L Quartile 1 1 1 1 Quartile 2 1.02 (0.44C2.37) 1.11 (0.17C7.06) 0.89 (0.33C2.38) Quartile 3 1.59 (0.78C3.24) 2.78 (0.61C12.62) 0.95 (0.36C2.49) Quartile 4 2.34 (1.12C4.88) 3.56 (0.81C15.72) 1.42 (0.30C6.82)Figure 5 Forrest plot for odds ratios of FGF-23 levels & median for short- and long-term survival grouped by baseline serum creatinine & median and & median. FGF-23 = fibroblast growth factor-23; OR = CI = confidence interval.DiscussionThe present study aimed to validate and extend preliminary findings from a prior study on plasma levels of the phosphaturic hormone FGF-23 in CS: we first confirm profoundly increased FGF-23 plasma levels in patients with infarction-related CS in a larger, bettercharacterized patient cohort within the randomized IABP-SHOCK II trial [9]. Second, we were able to show that increased FGF-23 levels are associated not only with increased shorttime (30-day) C as reported in our earlier study [9]C but also long-term (1-year) mortality. Third, the negative prognostic association of FGF-23 with both short- and long-time mortality persisted in multivariable analyses adjusted for several well-known prognostic factors. Fourth, the prognostic role of FGF-23 appears only to be relevant in patients with impaired renal function, as assessed by the baseline serum creatinine concentrations. The phosphaturic hormone FGF-23 is profoundly increased in patients with CKD [24] and associated with cardiovascular events and mortality [10,11]. Recently, understanding has emerged that this relationship is also present in apparently healthy individuals from the general population [14], in patients with prevalent cardiovascular disease [10] and in patients with stable chronic systolic heart failure [12,13]. As a pathophysiological explanation for these epidemiological findings, Faul et al. could show that FGF-23 exerts direct harmful pro-hypertrophic effects on myocardial tissue in vivo and in vitro [16]. Taken together, there is evidence from clinical and experimental studies thatFGF-23 may not only be a bystander, but a direct or indirect mediator of cardiovascular disease. However, a direct contribution of FGF-23 to myocardial disease is still under debate, after two further experimental studies failed to confirm a role of FGF-23 in left-ventricular hypertrophy [20,25]. The present data provide further evidence to the proposed reverse causality between elevated FGF-23 and cardiovascular disease according to which high FGF-23 secretion (hyperphosphatonism) not (only) induces cardiovascular disease, but instead prevalent subtle or overt cardiovascular disease may induce FGF-23 secretion. This hypothesis is underscored by our present observations that - as in our previous study [9] - FGF-23 levels in CS patients exceeded by far those found in patients with stable CAD, or in individuals with mild-to moderate CKD. Thus, it is unlikely that patients recruited into the present study had a substantial elevation of FGF-23 before they suffered CS, even though we cannot present formal evidence for this assumption. Interestingly, in several prospective epidemiologic studies, baseline FGF-23 levels did not predict future AMI [12,26] and in our previous study, patients with AMI without CS are characterized by FGF-23 levels comparable to those of stable CAD patients [9]. Thus, the profound rise in FGF-23 appears to be due to the neuroendocrinologic and/or hemodynamic impacts of CS rather than to the acute myocardial ischemia per se. A possible explanation for the increase in FGF-23 in CS might be the interplay between FGF-23, the renin-angiotensinaldosterone system (RAAS) [8,27] and the sympathetic activation [28]. Patients with CS are characterized by an activated RAAS and sympathetic system [29]. The increased RAAS activity down-regulates Klotho, an important cofactor of FGF-23 signaling, and leads to an up-regulation of FGF-23 [8]. Similarly, a role of sympathetic activation in FGF-23 secretion was proposed [28]. In the present study, the negative prognostic association of FGF-23 was not only observed with regard to short-term (30 days) but also to 1-year mortality. Furthermore, FGF-23 remained an independent predictor for mortality in a multivariate analysis including several factors known to affect risk of CS patients. Notably, regarding risk prediction of short-time mortality, FGF-23 was equally potent as serum lactate levels and combination of these two factors increased the diagnostic accuracy significantly. Interestingly, the negative prognostic association of FGF-23 was only observed in the patients with serum creatinine concentrations at baseline above the median, whereas in patients below the median, FGF-23 levels did not differ between survivors and non-survivors. These results are in line with previously published epidemiologic data, where associations to left ventricular hypertrophy and outcome have generally been stronger among individuals with impaired renal function [18,30]. As one example, cross-sectional data from the Heart and Soul Study, which recruited 887 patients with stable CAD and history of AMI, found an association between FGF-23 and left ventricular hypertrophy in individuals with estimated glomerular filtration rate & 60 ml/min/1.73 m2, but not in participants with intact renal function [20]. Patients with CKD are characterized by an activated vitamin D deficiency due to reduced 1α-hydroxylase activity. Low vitamin D has been shown to be a predictor of mortality in critically ill patients [31,32]. As vitamin D inhibits renin release, vitamin D deficiency is believed to increase RAAS-activity. This, in turn, might further promote the before-mentioned negative interplay between the RAAS and FGF-23 in CS. Increased RAAS activity leads to increased FGF-23 levels, which, in turn further impairs vitamin D activation [8].As a limitation to all epidemiologic studies, we cannot prove that elevated FGF-23 is causally linked to adverse outcome in CS. One potential mechanism might be above mentioned interplay between FGF-23 and Vitamin D. Moreover, recent evidence suggests that FGF-23 may contribute to volume retention, which further aggravates CS [33]. Alternatively, high FGF-23 may reflect preexisting CKD, or more severe left-ventricular disease, both of which directly contribute to poor outcome in CS. A further limitation of the study is its design as a single-center sub-analysis of a multicenter study.ConclusionsIn conclusion, our findings confirm in a large cohort study that patients with CS are characterized by profoundly increased FGF-23 levels. Beyond this, we show that in CS patients increased FGF-23 has a strong and independent negative prognostic association with short- and long-term outcome and that this association is observed only in patients with worse renal function. These results underline the need for future studies in order to clarify whether this association is causal or whether FGF-23 rather represents an innocent bystander, partly reflecting the underlying kidney damage, or more severe left-ventricular disease.Key messages? FGF-23 levels are an independent predictor of short- and long-term outcome in CS complicating AMI. ? These findings were only observed in patients with reduced kidney function.AbbreviationsAMI: Acute m AUC: A CAD: Cor CI: C CKD: Ch CS: C EF: Left ventricul FGF-23: Fibroblast growth factor 23; HR: H IABP: Intraaortic Balloon P IQR: I OR: O RAAS: Reninangiotensin-aldosterone system.Competing interestsAll authors declare that they have no conflicts of interest concerning the specific subject of this study. H.T: consulting fees from Eli Lilly, grant support on behalf of his institution from Eli Lilly and Terumo, and lecture fees from AstraZeneca, Boehringer Ingelheim, Daiichi Sankyo, Eli Lilly, the Medicines Company, and Terumo. M.B.: consulting fees from AstraZeneca, Bayer, Boehringer Ingelheim, Daiichi Sankyo, Medtronic, Merck, Novartis, Pfizer, Sanofi Aventis, and Servier and lecture fees from AstraZeneca, AWD.pharma Dresden, Bayer, Berlin-Chemie, Boehringer Ingelheim, Daiichi Sankyo, Merck, Novartis, Pfizer, Sanofi Aventis, and S J.P.: consulting fees from Sanofi Aventis. All other authors report no further conflict of interest.Authors’ contributionsGF: conception and design, data acquisition, analysis and interpretation of the data, drafting the manuscript. JP: conception and design, analysis and interpretation of the data, drafting the manuscript. DD: data acquisition, interpretation of the data, critical revision of the manuscript. SD: conception and design, interpretation of the data, critical revision of the manuscript. GHH: interpretation of the data, critical revision of the manuscript. IE: conception and design, interpretation of the data, critical revision of the manuscript. SS: interpretation of the data, critical revision of the manuscript. SdW: data acquisition, interpretation of the data, critical revision of the manuscript. SE: interpretation of the data, critical revision of the manuscript. AL: conception and design, interpretation of the data, critical revision of the manuscript. GS: conception and design, critical revision of the manuscript. VA: data acquisition, critical revision of the manuscript. MB: conception and design, interpretation of the data, critical revision of the manuscript. HT: conception and design, interpretation of the data, critical revision of the manuscript. All authors had full access to the data, take responsibility for the integrity of the data and the accuracy of the analysis, and have read and approved the final manuscript.Authors’ informationMichael B?hm and Holger Thiele share senior authorship.References1. Goldberg RJ, Samad NA, Yarzebski J, Gurwitz J, Bigelow C, Gore JM: Temporal trends in cardiogenic shock complicating acute myocardial infarction. N Engl J Med 62C1168. 2. Goldberg RJ, Spencer FA, Gore JM, Lessard D, Yarzebski J: Thirty-year trends (1975 to 2005) in the magnitude of, management of, and hospital death rates associated with cardiogenic shock in patients with acute myocardial infarction: a population-based perspective. Circulation 11C1219. 3. Kouraki K, Schneider S, Uebis R, Tebbe U, Klein HH, Janssens U, Zahn R, Senges J, Zeymer U: Characteristics and clinical outcome of 458 patients with acute myocardial infarction requiring mechanical ventilation. Results of the BEAT registry of the ALKKstudy group. 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