- Research article
- Open Access
- Open Peer Review
Would artificial neural networks implemented in clinical wards help nephrologists in predicting epoetin responsiveness?
© Gabutti et al; licensee BioMed Central Ltd. 2006
- Received: 01 June 2006
- Accepted: 18 September 2006
- Published: 18 September 2006
Due to its strong intra- and inter-individual variability, predicting the ideal erythropoietin dose is a difficult task. The aim of this study was to re-evaluate the impact of the main parameters known to influence the responsiveness to epoetin beta and to test the performance of artificial neural networks (ANNs) in predicting the dose required to reach the haemoglobin target and the monthly dose adjustments.
We did a secondary analysis of the survey on Anaemia Management in dialysis patients in Switzerland; a prospective, non-randomized observational study, enrolling 340 patients of 26 centres and in order to have additional information about erythropoietin responsiveness, we included a further 92 patients from the Renal Services of the Ente Ospedaliero Cantonale, Bellinzona, Switzerland. The performance of ANNs in predicting the epoetin dose was compared with that of linear regressions and of nephrologists in charge of the patients.
For a specificity of 50%, the sensitivity of ANNs compared with linear regressions in predicting the erythropoietin dose to reach the haemoglobin target was 78 vs. 44% (P < 0.001). The ANN built to predict the monthly adaptations in erythropoietin dose, compared with the nephrologists' opinion, allowed to detect 48 vs. 25% (P < 0.05) of the patients treated with an insufficient dose with a specificity of 92 vs. 83% (P < 0.05).
In predicting the erythropoietin dose required for an individual patient and the monthly dose adjustments ANNs are superior to nephrologists' opinion. Thus, ANN may be a useful and promising tool that could be implemented in clinical wards to help nephrologists in prescribing erythropoietin.
- Anaemia Management
- Clinical Ward
- Impaired Left Ventricular Ejection Fraction
Stable haemoglobin levels maintained in the target range of 11 to 12 g/dL as recommended by the Kidney Disease Outcomes Quality Initiative, are associated with both clinical and quality of life benefits as well as a reduction in hospitalisation and mortality [1–4]. Whether, in targeted subgroups, the haemoglobin concentration should be set above 12 g/dL has not been definitively demonstrated ; however, considering the likelihood of increasing thrombotic events [6, 7], its value should not exceed 14 g/dL .
The response to erythropoietin is known to have a large inter- and intra-individual variability explained by blood losses, co-morbidities , dialysis efficiency [9, 10], iron status [5, 11], folic acid and vitamin B12 deficiency , hyper- and hypo-parathyroidism [13, 14], pro-inflammatory cytokine activities , aluminium toxicity , treatment with angiotensin converting enzyme inhibitors (ACE-I)  and probably angiotensin II receptor blockers (ARB) . Thus, maintaining the haemoglobin level in the target range is sometimes a difficult task which necessitates regular doses adjustments.
To optimize anaemia management several protocols, based on physician or nurse-driven algorithm as well as computer assisted prescription tools, some of them involving the use of Artificial Neural Networks (ANNs), have been described [18–26].
A large amount of clinical and biochemical data that could be useful in making crucial follow-up decisions are actually collected during dialysis sessions [27–29]. Unfortunately the multidimensionality and at least partial non-linearity of the data, (i) limits the value of both intuition/experience of the nephrologists and standard statistical procedures and (ii) makes their interpretation and practical use in clinical wards difficult . The importance of individualizing drug dosage regimens by adding patient-specific post-administration data about serum levels or responsiveness to population pharmacokinetic and dynamic models, has been thoroughly demonstrated . Compared to other non linear mathematical and statistical tools based for instance on Bayesian fitting and adaptive control, ANNs have the advantage of being user friendly, tolerating missing data and errors in individual variables well and also of being applicable to translate multivariate non-linear relationships into continuous functions without the need of understanding precisely the underlying relationships between variables [31–36]. ANNs have been widely used in clinical medicine and have already assisted nephrologists in solving various complex clinical problems [27–33, 37, 38].
The purposes of the present study were (i) to characterize the linear or non-linear relationships between several clinical and biological variables and the response to epoetin beta and (ii) to build a computer assisted mathematical tool able to predict the epoetin requirement in an individual patient and the monthly adjustments in the epoetin dose.
We did a secondary analysis of the survey on Anaemia Management in dialysis patients in Switzerland (AIMS); a prospective, open label, non-randomized observational study designed to assess anaemia management in the dialysis centres in Switzerland [Lötscher N, et al. Swiss Med Forum 2004; 4: S7; Abstract]. In this study (inclusion and exclusion criteria were: current dialysis treatment, age > 18 y, renal anaemia requiring epoetin therapy, ferritin > 200 μg/L and respectively absence of vitamin B12 or folic acid deficiency, unstable angina pectoris, untreated hypertension, haemoglobinopathy, haemolysis, epilepsy), data about sex, weight, age, presence or absence of a diabetes mellitus and/or a cardiomyopathy, haemoglobin, epoetin beta dose and its administration route (subcutaneous vs. intravenous), ferritin and creatinine were collected in 340 hemodialysis patients. In order to increase the statistical power of the study and to gain more information about factors influencing erythropoietin responsiveness, a further 92 haemodialysis patients (with complete historical data and selected with the same criteria applied for the AIMS survey) were included in the analysis. These additional patients were selected based on the same inclusion criteria from the Renal Services of the Ente Ospedaliero Cantonale (EOC), Bellinzona, Switzerland after having been followed for at least 12 months (the 2 databases pooled together being called AIMSEOC data). For each patient the sex, weight and age, the haemoglobin, epoetin beta dose and its administration route (subcutaneous vs. intravenous), ferritin, creatinine, urea, Kt/V, pH, phosphate, ionized calcium, albumin, parathyroid hormone (PTH), C reactive protein (CRP) and intravenous iron dose over the 12 treatment months were collected. Comorbidity information about the concomitance of diabetes mellitus, cardiomyopathy with impaired left ventricular ejection fraction (<50%) and ACE-I or ARB medication were also registered.
The Kt/V, a parameter of dialysis adequacy defined as the dialyzer clearance of urea multiplied by the duration of the dialysis treatment and divided by the volume of distribution of urea in the body, was estimated with a second generation single-pool Daugirdas formula : Kt/V = -ln (R -0.03) + [(4-3.5 × R) × (UF/W)] where: R = post-dialysis urea/pre-dialysis urea, UF = net ultrafiltration and W = weight.
Estimation of the erythropoietin dose required to obtain a haemoglobin of 11.5 g/dL
To calculate the epoetin dose that should have been prescribed in order to obtain a haemoglobin of 11.5 g/dL a linear regression plotting epoetin dose against haemoglobin was built for each patient. The choice of using suboptimal tools like linear regressions to estimate the ideal epoetin dose was made considering that (i) the small number of observations reduced the statistical options at our disposal and (ii) an epoetin dose approximating the ideal one was necessary to build the models.
Artificial Neural Networks
In order to build the non-linear continuous functions expressing the interdependency between the collected data and the epoetin dose a series of artificial neural networks (ANNs) were built, trained, cross-validated and tested using the NeuroSolution for Excel 4.32 software, NeuroDimension Inc.
The databases selected to be analyzed were randomized using the same software package. After selecting 25% of the data for the validation phase, the remaining pool was divided into the training, cross validation and testing subgroups assigning respectively to each one 50, 10 and 40% of the data. As a network structure only Multilayer Perceptrons (MLP) (layered feed-forward networks trained with static backpropagation) and Generalized Feedforward Networks (GFN) (generalization of the MLP with connections jumping over hidden layers) were used (see Figure 1). Seeing that the critical difference between the two network structures is the amount of training data requested to optimize the performance (higher in the MLP and lower in the GFN) and because of the database with a limited extension used, each set of variables was used to train both models. A hyperbolic tangent transfer function (maximum and minimum output 1 and -1 respectively), as recommended by the producer (default setting), was chosen for each neuron. All initial connection weights were randomized before beginning a training phase. As a learning rule a gradient and weight change one (momentum) was chosen. To avoid overtraining, the training phase was stopped when the minimum squared error (MSE), displayed as a function of the training epochs, between the predictions and the desired output in the cross validation subgroup (indirect indicator of the level of generalisation) began to increase. All the networks were built using only one hidden layer while the ideal number of hidden neurons was determined by training, cross validating and testing a MLP, increasing unitarily the number of neurons beginning with 4 and stopping when the MSE between the predictions and the desired output in the testing subgroup began to increase. Once a definitive MLP was obtained, its performance was compared with a GFN with an identical number of processing elements (being both trained, cross validated and tested 5 times) and the best performing model (best compromise in the testing subgroup between linear correlation and normalized mean squared error r/NMSE) (see "Statistical and data analysis" paragraph for details) was selected to be tested in the validation subgroup. All studied variables were first analyzed separately and then combined in order to achieve the best prediction performance. The study was designed according to the prescriptions of Cross et al. .
Prediction by the nephrologists in charge of the patients of a follow-up haemoglobin level below the target of 11.0 g/dL
The sensitivity, specificity and the positive and negative predictive values in detecting a follow-up haemoglobin < 11.0 g/dL were calculated by interpreting the decision of the nephrologists to increase the epoetin dose as if it had been a prediction of a follow-up haemoglobin below the target level. Respecting statistical and modeling exigencies the haemoglobin measured one month after the adaptation in the dose has been considered as the follow-up haemoglobin.
Selection of the data for the prediction of the monthly epoetin dose adjustments
The data necessary to build and test the ANN predicting the monthly epoetin dose adjustments were selected from the AIMSEOC pool. Complete data of 4 consecutive months from months 3 to 6 and/or 7 to 10 were requested. The data of the months 3–5 and 7–9 were used as input while the data of months 6 and 10 were used as desired output.
Statistical and data analysis
Statistical and data analysis was performed using a statistical software package (SPSS 12.0; SPSS Inc.). SPSS was also used to build linear regressions (forward stepwise method based on the F probability including collinearity diagnostics) and to infer receiver-operating-characteristic curves (ROC) plotting the sensitivity against 1 minus the specificity for each prediction from the ANN, the linear regressions or the nephrologists (the areas under the curves were calculated by the trapezoidal nonparametric method and are expressed with the 95% confidence interval). Accuracy was expressed by the Combined Root Mean Square Error (CRMSE) calculated as the square root of [(mean difference in estimate-observed)2 + (standard deviation of the difference)2]. Agreement between the predictions and the basis data was expressed by "limits of agreement", "95% confidence interval for the bias" and "95% confidence interval for the lower and upper limits of agreement" according to Bland and Altman . The mean difference in estimate – observed, also called "bias", and the standard deviation of the difference of the same subtraction, also called "precision" are included concepts in both CRMSE and "limits of agreement". Histograms comparing the performance of the ANNs and the best performing linear regression were built using Excel SP3, Microsoft Inc. With the intention of facilitating the graphical representation of the differences in the predictive performances the ratio r/NMSE was calculated dividing the Pearson linear correlation coefficient r by the normalized mean squared error (obtained dividing the mean squared error by the variance of the reference population); the higher the value the better the performance. Percentages were compared using a Fisher exact test. The values are in mean ± standard deviation (SD). A P-value < 0.05 was considered statistically significant.
The 12-month follow-up of the AIMS survey was initiated in June 2002. 340 patients from 26 centres were included in the final analysis. The mean age of the participating patients was 63 ± 15 y. The most common causes of end-stage renal disease were glomerulonephritis (23%), diabetic nephropathy (21%) and hypertension (21%). The most prevalent baseline co-morbidities were cardiac-related. Hypertension occurred in 61% of the patients and diabetes was reported in 27%. The mean haemoglobin concentration was 11.8 ± 1.4 g/dl with approximately 80% of the included patients achieving the target haemoglobin of at least 11 g/dL. The mean epoetin beta dose was 149 ± 104 IU/kg/week.
Ninety-two patients (1104 monthly clinical and biochemical data) of the 3 dialysis units of the renal services of the Ente Ospedaliero Cantonale (EOC), Bellinzona, Switzerland, all meeting the requisite criteria, were also included in the analysis.
Characteristics of the studied populations
AIMS data (± SD)
EOCdata (± SD)
Sex (% of males)
63.5 ± 14.6
69.7 ± 12.1
69.5 ± 15.3
69.9 ± 15.4
Diabetes mellitus (%)
ACE-I or ARB treatment (%)
Haemoglobin g/dL b
11.8 ± 1.4
11.6 ± 0.7
Creatinine μmol/L b
580 ± 156
552 ± 145
BUN mmol/L b
24.6 ± 6.0
1.33 ± 0.26
7.36 ± 0.04
Phosphate mmol/L b
2.00 ± 1.38
Ionized calcium mmol/L b
1.20 ± 0.07
Albumin g/L b
37.9 ± 2.9
411 ± 297
482 ± 255
25.8 ± 21.9
CRP mg/L b
15.7 ± 15.8
Iron intravenously mg/month
134 ± 50
Epoetin beta dose IU/Kg/week to reach a haemoglobin of 11.5 g/dL
149 ± 104
107 ± 63
Epoetin administration route % of subcutaneous
Anaemia Management in dialysis patients in Switzerland
Renal units of the Ente Ospedaliero Cantonale, Bellinzona, Switzerland
AIMS and EOC data pooled
Artificial neural network
Angiotensin converting enzyme inhibitor or angiotensin receptor blocker treatment
Blood urea nitrogen a
Ionized calcium a
C reactive protein
Epoetin administration route subcutaneous vs. intravenous
normalized mean squared error divided by the Pearson correlation coefficient
Intra- and inter-individual variability of the epoetin dose
In the 2 databases pooled together (AIMSEOC data) the intra- and inter-individual variability in the epoetin dose prescribed, expressed by the mean absolute deviation from the mean, were 24.7 ± 27.1 and 49.8 ± 48.0 U/Kg/week (P < 0.001) respectively.
Linear correlations between variables and epoetin dose
In the same data pool the variables correlating significantly in a multiple linear regression with the epoetin dose (after intra- or extrapolation for a haemoglobin of 11.5 g/dL) were weight (standardized coefficient beta (β): -1.673; p < 0.001), ferritin (β: 0.079; P < 0.001), age (β: -0.800; P < 0.05), epoetin administration route (subcutaneous vs. intravenous) (β: -22.730; P < 0.05) and presence or absence of a cardiomyopathy (β: 33.050; P < 0.01). The obtained linear model with a constant of 301.686 (P < 0.001) explained 40.3 % of the variability in the epoetin dose (1.6 % imputable to the epoetin administration route; the intravenous one being associated with an epoetin dose 22.73 U/Kg/week higher). Taking the hemoglobin (before the intra- or extrapolation process) as a dependent variable, the epoetin dose (β: -0.003) and the epoetin administration route (subcutaneous vs. intravenous) (β:-0.528) were the only two significant variables (P < 0.001 in both cases) in building a linear model (constant: 12.980, R: 0.405). The epoetin administration route explained 10.2% of the haemoglobin variability in the model; the intravenous one being associated with a lower haemoglobin by 0.528 g/dL.
Non-linear correlations between variables and epoetin dose
Prediction of the epoetin requirement in an individual patient
The linear regressions, performed for each individual patient, plotting epoetin dose against haemoglobin with the aim of estimating the epoetin dose that should have been prescribed in order to obtain a haemoglobin of 11.5 g/dL, allowed, with a r value of 0.247 ± 0.237, to obtain an intrapolated value in 91% of the patients and an extrapolated one in 9%.
Prediction of the monthly epoetin dose adjustments
For the prediction of the monthly epoetin dose adjustments required to maintain the haemoglobin in the target range the training, cross-validation, testing and validation data pool consisted respectively of 200, 40, 140 and 110 monthly clinical and biochemical data taken from the AIMSEOC pool, including for each individual the haemoglobin and epoetin dose of the two previous months and the haemoglobin of the following one. The mean haemoglobin from the current observation (Hb), the 2 previous (Hb-1 and Hb-2) and the following (Hb+1) month and the mean epoetin dose from the current observation (EPO) and the 2 previous (EPO-1 and EPO-2) months were as follows: Hb: 11.51 ± 1.14, Hb-1: 11.55 ± 1.14, Hb-2: 11.54 ± 1.13, Hb+1: 11.52 ± 1.04, EPO: 83.97 ± 60.67, EPO-1: 87.05 ± 60.15, EPO-2: 85.34 ± 58.00. The remaining variables did not give a significant contribution in building an efficient non linear model and were excluded from the final algorithm.
Prediction ability of the nephrologists compared to ANNs
Mean absolute error
95% CI lower
95% CI upper
The sensitivity, the specificity, the positive and negative predictive value in predicting a follow-up haemoglobin < 11.0 g/dL of the best performing ANN compared with the nephrologists were 0.48 (27/56) versus 0.25 (14/56) P < 0.05, 0.92 (132/143) versus 0.83 (119/143) P < 0.05, 0.71 (27/38) vs. 0.39 (14/36) P < 0.01 and 0.82 (132/161) vs. 0.73 (119/162) n.s. respectively.
This study was performed in order to characterize once more the linear and non-linear relationship between several clinical and biological variables and the response to epoetin beta and to test the performance of non-linear mathematical models, based on artificial neural networks, in the prediction of the erythropoietin dose required for an individual patient. Our results show that ANNs which could be implemented in wards are clearly superior to linear regressions or the nephrologist's opinion in predicting the erythropoietin dose for an individual patient.
The first observation of this study is that linear regressions are less performant than ANNs as predictive tools. Indeed, as illustrated in Figure 3, in contrary to non-linear mathematical models based on ANNs, the best performing linear regression did not demonstrate any significant ability to predict erythropoietin responsiveness. This performance gap confirms a non-linear relationship between factors influencing both erythropoietin responsiveness and need in individual patients. As highlighted in previous studies [41, 42], on the basis of the results of the linear regressions, the administration route of erythropoietin significantly influenced the erythropoietin dose: patients treated with intravenous erythropoietin required a higher erythropoietin dose (16.0% more) and had lower haemoglobin (0.53 g/dL less).
Analysing the AIMSEOC data pool, the main variables influencing the mean erythropoietin dose needed to obtain a haemoglobin of 11.5 g/dL were weight, drug administration route (subcutaneous vs. intravenous), age and ferritin (see Figure 2 Panel A). Among these variables the relevance of the correlation with the weight has to be considered cautiously since the epoetin dose in the AIMSEOC database was indexed to body weight and in a previous study the absence of justification for body weight adjusted dosage was demonstrated . Confirming previous epidemiological and experimental data, the analysis of the EOC subgroup allowed the identification of further variables showing a relevant non linear relationship: particular attention should be given to pH, Kt/V, PTH and CRP (see Figure 2 Panel B) [9, 10, 13–15].
The good performance of the ANN built using as input variables weight, epoetin administration route, age, presence or absence of cardiomyopathy and creatinine is shown in Figure 3 (ROC curves). For a specificity of 50%, the sensitivity of ANNs compared with linear regressions in predicting the erythropoietin dose to reach the haemoglobin target was 78 vs. 44% (P < 0.001). Considering that the cited variables are included in the blood tests usually performed before starting an epoetin substitution, additional information about erythropoietin responsiveness could be easy obtained without supplementary costs.
Curiously enough not one of the cited variables contributed significantly in the building of the model structured to predict the monthly adaptations in epoetin dose in individual patients. This means that, as suggested by pharmacodynamic models for other drugs  and as confirmed by the results of previous studies [24, 26], the monthly fluctuations in haemoglobin as a function of the erythropoietin dose over a 3-month period are indirectly expressing all the other tested parameters related, in an analogous non linear mathematical model, to erythropoietin responsiveness. Of note, a large intra- and inter-individual variability in the requirements of erythropoietin (17.5 ± 19.2 and 35.3 ± 34.0 % respectively), to be referred at least in part to the inclusion in the study even of patients with intercurrent illnesses susceptible to influence the haemoglobin value, making the prediction of the ideal dose particularly difficult, was found in our database.
Comparative summary of the published studies
Number of patients/centres included
Variables explored (inputs)
Gabutti et al (present study)
Sex; age; weight, presence or absence of a diabetes mellitus and/or a cardiomyopathy with EF<50%; haemoglobin; creatinine; BUN; pH; ionized calcium; albumin; CRP; ferritin; PTH; epoetin and iron dose; epoetin administration route sc vs. iv; Kt/V
Epoetin dose and follow-up haemoglobin
Sex; age; haemoglobin; calcium; PTH; epoetin dose and others non specified
Martin Guerriero et al 
Alpha and beta
Age; weight; haemoglobin; ferritin; epoetin dose; isoform and number of administrations weekly; iron dose
Gaweda et al 
Haematocrit; albumin; ferritin; iron saturation; PTH; epoetin and iron dose; Kt/V
Jacobs et al 
Haematocrit; albumin; ferritin; iron saturation; PTH; epoetin and iron dose; Kt/V
Coming back to the choice of using ANNs as a non linear adaptive learning machine for individualizing epoetin dosage regimens, their usefulness by clinical ward oriented nephrologists has been demonstrated once again. However even if compared to other computer assisted mathematical models for non linear adaptive modeling ANNs are easy to use and to access and tolerate both missing data and errors in individual variables well, their user friendliness contrasts with the still persisting difficulties in correctly evaluating the reliability of the obtained functions [34–36].
The next step will be to include in the electronic documentation of the dialysis patients in use in our centres individualized models automatically warning the nephrologists about the need and modality of adaptations in the epoetin dose.
Compared with linear models, computer assisted tools based on artificial neural networks predict the mean erythropoietin dose required for an individual patient significantly better. Surprisingly using non linear correlations the most important variable influencing the epoetin requirement expressed in units/kg/week is the weight. Even if a particular attention should be reserved to both the pre-dialysis pH and the epoetin administration route, a prediction tool built with other variables known to influence the epoetin responsiveness will not increase in a quantitatively significant way the prediction power of the model.
As expected the model built to predict the dose adjustments is mainly influenced by the historical haemoglobin levels and even using only the data of the previous 2 months would allow compared with nephrologists, with a specificity of 92%, to detect a further 23% of the patients treated with an insufficient dose of erythropoietin.
Thus, implementing computer assisted tools that help predict the ideal erythropoietin dose, allowing timely and appropriate prescription adjustments, is an important challenge that will have relevant consequences on the patients' quality of life and should be further encouraged.
This work was funded by a grant from the Fondazione Ettore Balli, Locarno, Switzerland. The AIMS study was supported by Roche Pharma, Switzerland. We are indebted to Claudio Cereghetti, Carlo Schönholzer, Cele Vicari and Hugo Zwahlen who have been involved in data collection.
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