Patent Application
20110111526
Subject of the present invention is an in vitro method for the prediction of impaired peak oxygen consumption (VO2) for a subject not having a heart failure:
Another subject of the invention is the use of this method for risk assessment before non-cardiac surgery.
The clinical use of maximal cardiopulmonary exercise (CPET) with measurement of peak VO2 is well established (Cappuccio et al, Eur J Clin Invest 1991; 21:40-6; Benzo et al, Respir Med 2007; 101:1790-7; Bolliger et al, Am J Respir Crit. Care Med 1995; 151:1472-80; Brutsche et al, Bur Respir J 2000; 15:828-32; Butler et al, J Am Coll Cardiol 2004; 43:787-93; Isnard et al, Am J Cardiol 2000; 86:417-21; Isnard et al, Am Heart J 2003; 146:729-35). However, due to required equipment, time as well as a high degree of knowledge by both the technician and physician, CPET is not a broadly applied technique. Notably, estimation of peak VO2 based on the maximal workload achieved during a standard exercise test without gas exchange techniques, i.e. speed and grade of the treadmill or resistance of the bicycle ergometer, may be associated with significant inaccuracies, particularly in patients with low exercise capacity (Benzo et al, Chest 2007; 132:1500-5, Myers et al, J Am Coll Cardiol 1991; 17:1334-42), and is an insufficient alternative to CPET. Thus, rapidly and easily available alternatives to the assessment of peak VO2 would be highly desirable. In a previous study among patients with chronic heart failure (HF), B-type natriuretic peptide (BNP) has been proposed as a biochemical tool for the differentiation of patients with severely and moderately impaired exercise capacity (Kruger et al, J Am Coll Cardiol 2002; 40:718-22). (BNP is derived from a larger precursor peptide, proBNP, which can be proteolytically cleaved into BNP and N-terminal proBNP (NT-proBNP)). However, other studies in HF patients revealed that the correlation between BNP and peak VO2 might not be strong enough for reliable assessment of peak VO2 (Brunner-La Rocca et al, Heart 1999; 81:121-7, Maeder et al, Int J Cardiol 2007; 120:391-8). Furthermore, estimation of exercise capacity is required not only in HF patients. Similar studies for less selected patient groups and studies with other biomarkers are not available.
Thus, it was the objective of the present invention to find another marker as a surrogate for the assessment of peak VO2 by CPET. A surrogate marker according to the present invention is a substitute for the direct assessment of peak VO2 by CPET.
The marker assessed in the present invention is related to Endothelin-1. Endothelin (ET)-1 is a potent endothelium-derived endogenous vasoconstrictor (13). ET-1 exerts its vascular effects by activation of ET(A) and ET(B) receptors on smooth muscle cells, which causes an increase in intracellular calcium (Yanagisawa et al, J Hypertens Suppl 1988; 6:S188-91). Endogenous ET-1 contributes significantly to the vascular tone at rest (Spratt et al, Br Pharmacol 2001; 134:648-54), and ET(A) receptor-mediated vasoconstriction has been shown to account at least in part for the impaired vasodilatory response to exercise in hypertensive subjects (McEniery et al, Hypertension 2002; 40:202-6). Elevated ET-1 levels have been found in conditions associated with impaired exercise capacity, including post-myocardial infarction (Omland et al, Circulation 1994; 89:1573-9) and HF (Wei et al, Circulation 1994; 89:1580-6), but also chronic obstructive pulmonary disease (COPD) (Ferri et al, J Clin Pathol 1995; 48:519-24). In HF patients, a correlation between ET-1 and peak VO2 has been suggested previously (Kinugawa et al, J Card Fail 2003; 9:318-24). HF patients seem to exhibit an upregulation of neurohormones including ET-1 already without exercise testing. The effects of athletic strength and endurance exercise training in young humans on plasma endothelin-1 concentration and arterial distensibility have also been described (Otsuki et al., Experimental biology and medicine, 2006, 231, No. 6, 789-793).
Object of the present invention was the provision of a marker of peak VO2 in unselected patients, especially in subjects not having heart failure.
Thus, subject of the present invention is an in vitro method for the prediction of impaired peak VO2 (<14 ml/kg/min) for a subject not having heart failure:
In a preferred embodiment of the method according to the invention the sample was taken from said subject at rest and thus resting levels of Pro-Endothelin-1 (ProET-1) or fragments thereof of at least 12 amino acids are determined.
In another preferred embodiment of the method according to the invention the level of Pro-Endothelin-1 (ProET-1) or fragments thereof of at least 12 amino acids is additionally measured to maximal body weight-indexed bicycle workload (WLmax) and wherein the measurement of Pro-Endothelin-1 (ProET-1) or fragments thereof of at least 12 amino acids leads to an improvement in the accuracy of WLmax for the prediction of impaired peak VO2 (<14 ml/kg/min). WLmax is the maximal workload achieved during CEPT divided by the individual's body weight [Watt/kg].
VO2 max or peak VO2 (also maximal oxygen consumption, maximal oxygen uptake or aerobic capacity) is the maximum capacity of an individual's body to transport and utilize oxygen during incremental exercise, which reflects the physical fitness of the individual. VO2 max is properly defined by the Fick Equation: VO2 max=Q(CaO2−CvO2), wherein Q is the cardiac output of the heart, CaO2 is the arterial oxygen content, and CvO2 is the venous oxygen content. In general clinical and athletic testing, the measuring of VO2 max usually involves a graded exercise test (either on a treadmill or on a cycle ergometer) in which exercise intensity is progressively increased while measuring ventilation and oxygen and carbon dioxide concentration of the inhaled and exhaled air. VO2 max is reached when oxygen consumption remains at steady state despite an increase in workload. VO2 max is widely accepted as a good measure of cardiovascular fitness and maximal aerobic power.
A surrogate marker according to the present invention is a substitute for the direct assessment of peak VO2 by CPET.
The appraisal of peak VO2 (VO2 max) has to take into consideration the individual's gender and age. A peak VO2 of 14 (ml/kg/min) or less can be considered as severely reduced, since frequently it qualifies for a heart transplantation (http://www.brianmac.co.uk/vo2max.htm see
Endothelin-1 is derived from a larger precursor molecule named Pro-Endothelin-1. Pro-Endothelin-1 can be proteolytically processed into various fragments as described (Struck J, Morgenthaler N G, Bergmann A. Proteolytic processing pattern of the endothelin-1 precursor in vivo. Peptides. 2005 December; 26(12):2482-6.). These fragments are subject to proteolytic degradation in the blood circulation, which can happen quickly or slowly, depending on the type of fragment and the type and concentration/activity of proteases present in the circulation. Thus, according to the present invention the level of any of these fragments of at least 12 amino acids may be measured, preferably fragments of at least 20 amino acids, more preferably of at least 30 amino acids, Preferably, C-terminal pro-ET-1 (CT-proET-1) or a fragment thereof may be measured.
In another preferred embodiment of the invention the level of proBNP or fragments thereof of at least 12 amino acids including BNP or NT-proBNP is measured in addition to WLmax and wherein the measurement of proBNP or fragments thereof of at least 12 amino acids leads to an improvement in the accuracy of WLmax for the prediction of impaired peak VO2. Thus, according to the present invention the level of any of these fragments of at least 12 amino acids may be measured, preferably fragments of at least 20 amino acids, more preferably of at least 30 amino acids.
In an especially preferred embodiment both the level of Pro-Endothelin-1 (ProET-1) or fragments thereof of at least 12 amino acids and proBNP or fragments thereof of at least 12 amino acids including BNP or NT-proBNP is measured in addition to WLmax and wherein the measurement of Pro-Endothelin-1 (ProET-1) or fragments thereof of at least 12 amino acids and proBNP or fragments thereof of at least 12 amino acids including BNP or NT-proBNP leads to an improvement in the accuracy of WLmax for the prediction of impaired peak VO2.
When CT-proET-1 and BNP are used as fragments of their precursors, preferable cut-off values are 74.4 pmol/L and 35.9 pg/mL, respectively. Thus, the use of these two biomarkers in combination with a standard exercise test for the prediction of a severely impaired peak VO2 is subject of the present invention.
Subject of the present invention is further the use of Pro-Endothelin-1, preferably CT-proET-1, in clinical practice in situations where a semi-quantitative estimate of peak VO2 seems sufficient, e.g., for risk assessment before non-cardiac surgery. For low- or medium-risk surgery in patients without significant risk factors such as angina, symptomatic HF, or diabetes, guidelines suggest an exercise capacity threshold of four metabolic equivalents as the criterion to decide about the need for additional non-invasive tests (Eagle et al, Circulation 2002; 105:1257-67).
Thus, subject of the present invention is the use of CT-proET-1 for preoperative risk assessment. One might also consider a combination of BNP and CT-proET-1.
According to the present invention said sample that is obtained from a subject not having heart failure is selected from the group comprising a blood sample, a serum sample, and a plasma sample.
According to a preferred embodiment of the invention said level of CT-proET-1 (or fragments thereof) is measured with a sandwich immunoassay. An example for such sandwich immunoassay has been described (Papassotiriou J, Morgenthaler N G, Struck J, Alonso C, Bergmann A. Immunoluminometric assay for measurement of the C-terminal endothelin-1 precursor fragment in human plasma. Clin Chem. 2006 μm; 52(6):1144-51.)
Instead of Pro-Endothelin-1 (ProET-1) or fragments thereof another surrogate marker may be used selected from the group comprising Pro-Adrenomedullin or fragments thereof of at least 12 amino acids including MR-proADM, CT-proADM, Adrenomedullin and PAMP (DE 103 16 583.5; DE 10 2006 060 11; Beltowski J, Jamroz A. Adrenomedullin—what do we know 10 years since its discovery? Poi J. Pharmacol. 2004 January-February; 56(1):5-27; Struck J, Tao C, Morgenthaler N G, Bergmann A. Identification of an Adrenomedullin precursor fragment in plasma of sepsis patients. Peptides. 2004 August; 25(8):1369-72.).
In the context of the present invention, the term “level” as referring to levels of markers, refers to the quantity of the molecular entity mentioned in the respective context, or in the case of enzymes it can also refer to the enzyme activity.
As mentioned herein in the context of proteins or peptides, the term “fragment” refers to smaller proteins or peptides derivable from larger proteins or peptides, which hence comprise a partial sequence of the larger protein or peptide. Said fragments are derivable from the larger proteins or peptides by saponification of one or more of its peptide bonds.
As mentioned herein, an “assay” or “diagnostic assay” can be of any type applied in the field of diagnostics. Such an assay may be based on the binding of an analyte to be detected to one or more capture probes with a certain affinity. Concerning the interaction between capture molecules and target molecules or molecules of interest, the affinity constant is preferably greater than 108M−1.
Preferred detection methods comprise immunoassays in various formats such as for instance radioimmunoassays, chemiluminescence- and fluorescence-immunoassays, Enzyme-linked immunoassays (ELISA), Luminex-based bead arrays, protein microarray assays, and rapid test formats such as for instance immunochromatographic strip tests.
The assays can be homogenous or heterogeneous assays, competitive and non-competitive sandwich assays. In a particularly preferred embodiment, the assay is in the form of a sandwich assay, which is a noncompetitive immunoassay, wherein the molecule to be detected and/or quantified is bound to a first antibody and to a second antibody. The first antibody may be bound to a solid phase, e.g. a bead, a surface of a well or other container, a chip or a strip, and the second antibody is an antibody which is labeled, e.g. with a dye, with a radioisotope, or a reactive or catalytically active moiety. The amount of labeled antibody bound to the analyte is then measured by an appropriate method. The general composition and procedures involved with “sandwich assays” are well-established and known to the skilled person. (The Immunoassay Handbook, Ed. David Wild, Elsevier LTD, Oxford; 3rd ed. (May 2005), ISBN-13: 978-0080445267; Hultschig C et al., Curr Opin Chem. Biol. 2006 February; 10(1):4-10. PMID: 16376134), incorporated herein by reference.
In a particularly preferred embodiment the assay comprises two capture molecules, preferably antibodies which are both present as dispersions in a liquid reaction mixture, wherein a first marking component is attached to the first capture molecule, wherein said first marking component is part of a marking system based on fluorescence- or chemiluminescence-quenching or amplification, and a second marking component of said marking system is attached to the second capture molecule, so that upon binding of both capture molecules to the analyte a measurable signal is generated that allows for the detection of the formed sandwich complexes in the solution comprising the sample.
Even more preferred, said marking system comprises rare earth cryptates or rare earth chelates in combination with a fluorescence dye or chemiluminescence dye, in particular a dye of the cyanine type.
In the context of the present invention, fluorescence based assays comprise the use of dyes, which may for instance be selected from the group comprising FAM (5- or 6-carboxyfluorescein), VIC, NED, Fluorescein, Fluoresceinisothiocyanate (FITC), IRD-700/800, Cyanine dyes, auch as CY3, CY5, CY3.5, CY5.5, Cy7, Xanthen, 6-Carboxy-2′,4′,7′,4,7-hexachlorofluorescein (HEX), TET, 6-Carboxy-4′,5′-dichloro-2′,7′-dimethodyfluorescein (JOE), N,N,N′,N′-Tetramethyl-6-carboxyrhodamine (TAMRA), 6-Carboxy-X-rhodamine (ROX), 5-Carboxyrhodamine-6G (R6G5), 6-carboxyrhodamine-6G (RG6), Rhodamine, Rhodamine Green, Rhodamine Red, Rhodamine 110, BODIPY dyes, such as BODIPY TMR, Oregon Green, Coumarines such as Umbelliferone, Benzimides, such as Hoechst 33258; Phenanthridines, such as Texas Red, Yakima Yellow, Alexa Fluor, PET, Ethidiumbromide, Acridinium dyes, Carbazol dyes, Phenoxazine dyes, Porphyrin dyes, Polymethin dyes, and the like.
In the context of the present invention, chemiluminescence based assays comprise the use of dyes, based on the physical principles described for chemiluminescent materials in Kirk-Othmer, Encyclopedia of chemical technology, 4th ed., executive editor, J. I. Kroschwitz; editor, M. Howe-Grant, John Wiley & Sons, 1993, vol. 15, p. 518-562, incorporated herein by reference, including citations on pages 551-562. Preferred chemiluminescent dyes are Acridiniumesters.
In the context of assays, “capture probes” are molecules which may be used to bind target molecules or molecules of interest, i.e. analytes, from a sample. Capture molecules must thus be shaped adequately, both spatially and in terms of surface features, such as surface charge, hydrophobicity, hydrophilicity, presence or absence of lewis donors and/or acceptors, to specifically bind the target molecules or molecules of interest. Hereby, the binding may for instance be mediated by ionic, van-der-Waals, pi-pi, sigma-pi, hydrophobic or hydrogen bond interactions or a combination of two or more of the aforementioned interactions between the capture molecules and the target molecules or molecules of interest. In the context of the present invention, capture molecules may for instance be selected from the group comprising a nucleic acid molecule, a carbohydrate molecule, a PNA molecule, a protein, an antibody, a peptide or a glycoprotein. Preferably, the capture molecules are antibodies, including fragments thereof with sufficient affinity to a target or molecule of interest, and including recombinant antibodies or recombinant antibody fragments, as well as chemically and/or biochemically modified derivatives of said antibodies or fragments derived from the variant chain with a length of at least 12 amino acids thereof.
As used herein, terms such as “marker” “prognostic marker(s), parameter(s) or factor(s)” or “biomarker” or “biological marker” are used interchangeably and relate to measurable and quantifiable biological parameters (e.g., specific enzyme concentration, specific hormone concentration, specific gene phenotype distribution in a population, presence of biological substances) which serve as indices for health- and physiology-related assessments, such as disease risk, psychiatric disorders, environmental exposure and its effects, disease diagnosis, metabolic processes, substance abuse, pregnancy, cell line development, epidemiologic studies, etc. Furthermore, a biomarker is defined as a characteristic that is objectively measured and evaluated as an indicator of normal biological processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention. A biomarker may be measured on a biosample (as a blood, urine, or tissue test), it may be a recording obtained from a person (blood pressure, ECG, or Halter), or it may be an imaging test (echocardiogram or CT scan) (Vasan et al. 2006, Circulation 113:2335-2362).
Biomarkers can indicate a variety of health or disease characteristics, including the level or type of exposure to an environmental factor, genetic susceptibility, genetic responses to exposures, biomarkers of subclinical or clinical disease, or indicators of response to therapy. Thus, a simplistic way to think of biomarkers is as indicators of disease trait (risk factor or risk biomarker), disease state (preclinical or clinical), or disease rate (progression). Accordingly, biomarkers can be classified as antecedent biomarkers (identifying the risk of developing an illness), screening biomarkers (screening for subclinical disease), diagnostic biomarkers (recognizing overt disease), staging biomarkers (categorizing disease severity), or prognostic biomarkers (predicting future disease course, including recurrence and response to therapy, and monitoring efficacy of therapy). Biomarkers may also serve as surrogate end points. A surrogate end point is one that can be used as an outcome in clinical trials to evaluate safety and effectiveness of therapies in lieu of measurement of the true outcome of interest. The underlying principle is that alterations in the surrogate end point track closely with changes in the outcome of interest. Surrogate end points have the advantage that they may be gathered in a shorter time frame and with less expense than end points such as morbidity and mortality, which require large clinical trials for evaluation. Additional values of surrogate end points include the fact that they are closer to the exposure/intervention of interest and may be easier to relate causally than more distant clinical events. An important disadvantage of surrogate end points is that if clinical outcome of interest is influenced by numerous factors (in addition to the surrogate end point), residual confounding may reduce the validity of the surrogate end point. It has been suggested that the validity of a surrogate end point is greater if it can explain at least 50% of the effect of an exposure or intervention on the outcome of interest. For instance, a biomarker may be a protein, peptide or a nucleic acid molecule.
“Subjects” in the meaning of the invention are understood to be all persons or animals, irrespective whether or not they exhibit pathological changes, unless stated otherwise. In the meaning of the invention, any sample collected from cells, tissues, organs, organisms or the like can be a sample of a patient to be diagnosed. In a preferred embodiment the subject according to the invention is a human.
A “Sample” in the meaning of the invention can be all biological tissues and all fluids such as lymph, urine, cerebral fluid, blood, saliva, serum, or faeces. Tissues may be, e.g. epithelium tissue, connective tissue such as bone or blood, muscle tissue such as visceral or smooth muscle and skeletal muscle and, nervous tissue, bone marrow, cartilage, skin, mucosa or hair. The sample is collected from the patient or subjected to the diagnosis according to the invention. Where appropriate, as for instance in the case of solid samples, the sample may need to be solubilized, homogenized, or extracted with a solvent prior to use in the present invention in order to obtain a liquid sample. A liquid sample hereby may be a solution or suspension. Liquid samples may be subjected to one or more pre-treatments prior to use in the present invention. Such pre-treatments include, but are not limited to dilution, filtration, centrifugation, concentration, sedimentation, precipitation, or dialysis. Pre-treatments may also include the addition of chemical or biochemical substances to the solution, such as acids, bases, buffers, salts, solvents, reactive dyes, detergents, emulsifiers, or chelators.
Title: Relationship between peak oxygen consumption, external workload and biomarkers Caption: Scatter plots illustrating the correlations between peak oxygen consumption (peak VO2) and B-type natriuretic peptide (BNP, panel A), C-terminal-pro-endothelin-1 (CT-proET-1, panel B), and the maximal body weight-indexed external bicycle workload (WLmax, panel C) and as well as the correlation between BNP and CT-proET-1 (panel D). Spearman correlation coefficients are given. Note the logarithmic scale for peak VO2 and BNP.
Title: Accuracy of biomarkers alone or combined with external workload for the prediction of a peak oxygen consumption <14 ml/kg/min.
Caption: Panel A: Receiver-operator-characteristics (ROC) curves showing the AUC (with 95% confidences intervals) for the prediction of a peak VO2<14 ml/kg/min for B-type natriuretic peptide (BNP) and C-terminal-pro-endothelin-1 (CT-proET-1) at rest. Panel B: ROC curves showing the AUC (with 95% confidences intervals) for the prediction of a peak VO2<14 ml/kg/min for BNP and CT-proET-1 at rest and at peak exercise. Panel C: ROC curves showing the AUC for the prediction of a peak VO2<14 ml/kg/min for BNP and CT-proET-1 at rest and the maximal body weight-indexed external bicycle workload (WLmax). For better comparison with BNP and CT-proET-1 the ROC curve for 1/WLmax is shown. In addition, sensitivity and 1-specificity of the combinations of optimal cut-offs for WLmax with optimal cut-offs for CT-proET-1 and BNP are shown. The arrows indicate sensitivity and 1-specificity of the optimal WLmax cut-off (→) and combinations of WLmax, CT-proET-1, and BNP to achieve optimal specificity or sensitivity
.
VO2 max average ranges for women and men.
(a) Receiver-operator-characteristics (ROC) curves showing the areas under the curve (AUC) for B-type natriuretic peptide (BNP), the BNP-based five-item score, and the six-item score [addition of C-terminal-pro-endothelin-1 (CT-pre-ET-1)] for the prediction of a peak oxygen consumption (peak VO2)<14 mL kg−1 min−1.
(b) ROC curves showing the AUC for CT-proET-1, the CT-proET-1-based five-item score, and the six-item score (addition of BNP) for the prediction of a peak VO2<14 mL kg−1 min−1.
The present study of a representative sample of unselected patients referred for CPET revealed two important findings: First, CT-proET-1 measured at rest was related to peak VO2 and had a high accuracy in predicting a severely impaired peak VO2 and thereby outperformed BNP. Second, additional measurement of CT-proET-1 and BNP led to a marked improvement in the accuracy of WLmax for the prediction of severely impaired peak VO2.
From May 2004 to June 2005, 185 consecutive patients referred for CPET for the evaluation of unexplained exercise intolerance were eligible for inclusion. We excluded patients without informed consent (n=12) and patients without CT-pro-ET-1 and/or BNP determination (n=11). This left a total of 162 patients for the present analysis. This study was approved by the local ethics committee. Written informed consent was obtained from all participating patients.
Patients underwent symptom-limited upright bicycle exercise using routine protocols with a 12-lead electrocardiogram recording each minute of exercise and continuous monitoring of the electrocardiogram throughout the test. The following test end points were applied: physical exhaustion, severe angina, sustained ventricular arrhythmia or exertional hypotension. Expired gases were acquired continuously, and oxygen uptake (VO2) and carbon dioxide output (VCO2) were recorded in rolling 30 second averages. Calibration of the system was performed before each test with a 3-liter syringe. The respiratory exchange ratio respiratory exchange ration (RER), defined as VCO2 divided by VO2, was determined throughout the test. Maximal effort was assumed if at least one of the following criteria was fulfilled: 1. peak heart rate >80% predicted, 2. RER >1.2, 3. lactate at peak exercise >4.5 mmol/l, or 4. base excess >−2.5 mmol/l (Schmid et al, Respirology 2007; 12:916-23). These criteria have been used in our CPET laboratory for years and reflect the principles outlined in the guidelines of the American Thorax Society/Amercian College of Chest Physicians (ATS/ACCP Statement on cardiopulmonary exercise testing, Am J Respir Crit. Care Med 2003; 167:211-77). Exercise capacity was expressed as directly measured peak VO2 and the maximal body weight-indexed external bicycle workload (WLmax).
A specimen of venous blood was drawn before and one minute after peak exercise in the seated position from a catheter previously inserted into the antecubital vein. These samples were collected in plastic tubes containing ethylene-diamin-tetra-acetate. They were placed on ice and then centrifuged at 3,000 g; and plasma was frozen at −80° C. All plasma samples were analyzed approximately one year after collection. The laboratory technician who performed the assays was at a different site and blinded to patients characteristics and CPET results. CT-proET-1 was detected using a novel commercially available assay in the chemiluminescence/coated tube-format (BRAHMS AG, Hennigsdorf/Berlin, Germany) as previously described (Papassotiriou et al, Clin Chem 2006; 52:1144-51; Khan et al, Am Heart J 2007; 154:736-42). BNP concentration was determined using the commercially available AxSYM BNP assay (Abbott Laboratories, Zug, Switzerland) (Mueller et al, Clin Chem 2004; 50:1104-6). This fully automated microparticle enzyme immunoassay uses two monoclonal mouse antibodies in a two-step format. Being harmonized to the Biosite BNP assay, it has a dynamic range of 1-4000 pg/ml.
Data were expressed as numbers and percentages, mean±standard deviation, and median (interquartile range) unless otherwise indicated. Normal distribution of the data was tested with the use of the Kolmogorov-Smirnov test. Comparisons were made using chi-square or Fisher exact tests, unpaired t-tests, or nonparametric tests as appropriate. To compare BNP (log-transformed due to skewed distribution) and CT-proET-1 levels at rest and at peak exercise analysis of variance for repeated measures was performed. Correlations between parameters of interest were performed using Spearman correlation coefficients.
ROC curves were constructed to assess the sensitivity and specificity of CT-proET-1 and BNP throughout the concentrations and WLmax to detect a peak VO2<14 ml/kg/min. This cut-off was selected based on its established prognostic value in patients with HF (Cappuccio et al, Eur J Clin Invest 1991; 21:40-6) and the fact that it corresponds to four metabolic equivalents, which is a frequently used cut-off for the differentiation of severely and moderately impaired exercise capacity for preoperative risk stratification (Eagle et al, Circulation 2002; 105:1257-67). Sensitivity, specificity, positive predictive value, and negative predictive values for optimal cut-offs of biomarkers and WLmax as well as their combination were calculated. ROC curves were compared using the method by DeLong et al. (DeLong et al, Biometrics 1988; 44:837-45) using a specialized software (Analyse-it V2.04, Leeds, UK). All other statistical analyses were performed using SPSS/PC (version 15.0, SPSS Inc, Chicago, Ill.). All hypothesis testing was two-tailed. A p value <0.05 was considered statistically significant.
Characteristics of patients achieving a peak VO2<14 ml/kg/min (n=39) versus ml/kg/min (n=123) are presented in Table 1. Patients with a peak VO2<14 ml/kg/min were older, more overweight, were more likely to have coronary artery disease, peripheral arterial obstructive disease, chronic obstructive pulmonary disease, and pulmonary hypertension, were more likely to be treated with beta blockers, inhibitors of the renin-angiotensin-aldosterone system, diuretics, nitrates, aspirin, and statins, and were more symptomatic than patients with peak VO2≧14 ml/kg/min.
Results from CPET are shown in Table 2. Peak heart rate, peak systolic blood pressure, and per definition, measures of exercise capacity were lower in patients with peak VO2<14 ml/kg/min than in those with peak VO2>14 ml/kg/min. The forced expiratory volume within the first second and the ratio of the forced expiratory volume within the first second to forced vital capacity was lower, and the resting respiratory rate was higher in patients with a peak VO2<14 ml/kg/min. The arterial pressure of oxygen at peak exercise but not at rest and the arterial carbon dioxide pressure at rest but not at peak exercise were lower, and the alveolo-arterial gradient both at rest and at peak exercise was higher in patients with a peak VO2<14 ml/kg/min as compared to those with a peak VO2≧14 ml/kg/min.
In Table 3, biomarker levels at rest and at peak exercise as well as absolute and relative changes from rest to peak exercise in patients with a peak VO2<14 ml/kg/min versus 14 ml/kg/min are displayed. CT-proET-1 and BNP levels at rest (p<0.001 for both) and at peak exercise (p<0.001 for both) were higher in patients with a peak VO2<14 ml/kg/min as compared to those with a peak VO2 ml/kg/min. There was a significant increase in CT-pro-ET-1 and BNP from rest to peak exercise in both patients with peak VO2<14 ml/kg/min and ≧14 ml/kg/min. Absolute and relative changes in CT-proET-1 and BNP were similar in both groups.
As shown in
CT-proET-1 and BNP at Rest for the Prediction of a Peak VO2<14 ml/kg/min
In
CT-proET and BNP at Peak Exercise for the Prediction of a Peak VO2<14 ml/kg/min
In
WLmax Combined with Biomarkers for the Prediction of a Peak VO—<14 ml/kg/min
As expected, WLmax had a high albeit not perfect accuracy for the prediction of a peak VO2≧14 ml/kg/min [AUG 0.92 (95% CI 0.88-0.96); p<0.001]. An optimal cut-off of 1.22 Watts/kg had a sensitivity of 87% and a specificity of 85%. As shown in
In Table 4, test characteristics of the optimal cut-offs for WLmax and the biomarkers as well as their combinations are shown. The added use of CT-proET-1 or/and BNP improved specificity and the positive predictive value of WLmax for the prediction of a peak VO2<14 ml/kg/min from 85% and 65%, respectively to up to 97% and 85%, respectively. On the other hand, there was no patient without any pathological test value (ie. BNP <35.9 pg/ml, CT-pro-ET<74.4 pmol/l, WLmax>1.22 Watt/kg) who had a peak VO2<14 ml/kg/min, ie. sensitivity and negative predictive value of this combination were 100%, whereas sensitivity and negative predictive value of the optimal WLmax cut-off alone were 85% and 95%, respectively.
In
BNP and CT-proET-1 combined with other parameters for the prediction of a peak VO2<14 mL kg−1 min−1
The AUC for FEV1, D(A-a)O2 and BMI for the prediction of a peak VO2<14 mL kg−1 min−1 were 0.77 [95% confidence interval (95% CI) 0.68-0.87; P<0.001], 0.76 (95% CI 0.66-0.85; P<0.001) and 0.65 (95% CI 0.53-0.78; P=0.01) respectively. Optimal cut-offs and test characteristics are shown in Table 4. The AUC for PaCO2 did not reveal a statistically significant result (P=0.07). A five-item score with one score point for FEV1<1.88 L, D(A-a)O2>28 mmHg, BMI>28 kg m−2, presence of diabetes and BNP >37.2 pg mL−1 had an AUC of 0.88 (
The accuracy of the two biomarkers for the prediction of a peak VO2<20 mL kg−1 min−1 (n=90), which is the cut-off for an impaired exercise capacity according to the Weber classification (Weber et al., Circulation 1987; 76: VI40-5.) was also determined. The AUC for BNP and CT-proET-1 were 0.76 (95% CI 0.68-0.84; P<0.001) and 0.75 (95% CI 0.67-0.84; P<0.001) respectively. In contrast, the AUC for BNP and CT-proET-1 for the prediction of a peak VO2≦84% of the predicted value (n=103), which is the cut-off for an impaired exercise capacity according to CPET guidelines (ATS/ACCP statement on cardiopulmonary exercise testing, Am J Respir Crit. Care Med 2003; 167: 211-77.) were only 0.63 (95% CI 0.53-0.73; P=0.02) and 0.58 (95% CI 0.47-0.68; P=0.17) respectively.
| Number | Date | Country | Kind |
|---|---|---|---|
| 08154267.2 | Apr 2008 | EP | regional |
| 09151573.4 | Jan 2009 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2009/054251 | 4/8/2009 | WO | 00 | 12/28/2010 |
