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Int J Med Sci 2020; 17(7):970-984. doi:10.7150/ijms.42078 This issue Cite

Research Paper

Role of Artificial Intelligence in Kidney Disease

Qiongjing Yuan^1#, Haixia Zhang^1,2#, Tianci Deng¹, Shumei Tang¹, Xiangning Yuan¹, Wenbin Tang¹, Yanyun Xie¹, Huipeng Ge¹, Xiufen Wang¹, Qiaoling Zhou¹, Xiangcheng Xiao¹

1. Department of Nephrology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan 410008, China
2. Department of Nephrology, Second Affiliated Hospital of Soochow University, 1055 Sanxiang Road, Suzhou, Jiangsu 215000, China
#Equal contribution.

✉ Corresponding author: Xiangcheng Xiao (E-mail: xiaoxcedu.cn).

Abstract

Artificial intelligence (AI), as an advanced science technology, has been widely used in medical fields to promote medical development, mainly applied to early detections, disease diagnoses, and management. Owing to the huge number of patients, kidney disease remains a global health problem. Challenges remain in its diagnosis and treatment. AI could take individual conditions into account, produce suitable decisions and promise to make great strides in kidney disease management. Here, we review the current studies of AI applications in kidney disease in alerting systems, diagnostic assistance, guiding treatment and evaluating prognosis. Although the number of studies related to AI applications in kidney disease is small, the potential of AI in the management of kidney disease is well recognized by clinicians; AI will greatly enhance clinicians' capacity in their clinical practice in the future.

Keywords: Artificial intelligence, kidney disease, Alerting systems, Diagnostic assistance, Guiding treatment, Evaluating prognosis

Introduction

Kidney disease is a major public health problem in part because of its common etiology caused by diabetes, hypertension, obesity, and aging; the incidence of these conditions is increasing. According to the Global Burden of Diseases, Injuries, and Risk Factors Study 2015, 750 million people worldwide suffered from kidney disease [1]. Kidney disease brings a huge burden to society. In 2017, a survey showed that the yearly cost was approximately $1,205 for a patient with stage 3 chronic kidney disease (CKD3), $1963 for a CKD4 individual, $8,035 for a person at CKD5 condition, and $34,554 for a hemodialysis patient [2]. Early detection and prevention of the progression of kidney disease towards end stage renal disease is therefore of significant importance.

AI is a science of computer simulated thinking processes and human behaviors, which involves computer science, psychology, philosophy and linguistics. In 2016, Alphago 3-0 won a professional human Go player. It was the first computer program that defeated a world champion of Go, clearly revealing the potential that AI will bring technological advances in the era. The continued rapid growth in computer-processing power over the past two decades, the availability of large data sets and the development of advanced algorithms have driven major improvements in machine learning[3].

Electronic medical records (EMR) provide large-scale and real-world clinical data, which is the basis for developing AI technology in the clinic. It is challenging for humans to directly analyze these massive data; this is not only because of the massive time required and cares needed to avoid human errors but also the ability to derive the insights or information in depth. Clearly, AI technology holds nonparallel advantages over humans in these domains [4]. The studies of AI in kidney diseases are at a beginning stage. According to the existing literature, the function of AI in kidney disease mainly focuses on four aspects: Alerting systems, Diagnostic assistance, Guiding treatment and Evaluating prognosis.

Materials and Methods

Data source

A non-systematic review of the literature was performed by screening PubMed up to 1st of August 2019. Using the search terms including "artificial intelligence", "machine learning", “artificial neuron networks”, “deep learning”, "kidney Disease", "chronic kidney disease" , "acute kidney Injury" and “nephrology”.

Study selection

Literature was derived from English articles or articles that could be obtained with English abstracts. Studies of human dataset were included. References were also identified from the bibliographies of identified articles and the authors' files.

The function of AI in kidney disease: Alerting systems, Diagnostic assistance, Guiding treatment and Evaluating prognosis

Alerting systems

Early prediction of deterioration can play an important role in supporting health care professionals, as an estimated 11 percent of hospital deaths follow a failure to promptly recognize and treat deteriorating patients [5].AI can identify information quickly and effectively, explore intrinsic relationship.

Alerting AKI

It is reported that AI technology has an advantage in warning of critical illness, such as acute kidney injury (AKI) [6]. AKI is a common critical illness in clinic, especially for elderly and perioperative patients. The incidence of AKI was 7-18% among hospitalized and 50% in ICU patients [7], and it was increasing by 11% per year [8]. AKI would prolong hospitalization and increase the cost of treatment [9]. Patients with AKI would be more likely to progress to end-stage renal disease (ESRD) than those without AKI [10]. There were approximately 2 million patients died of AKI every year. The mortality rate was 10-30% for AKI patients without complication, and 30-80% for those with multiple organ failure [11]. At present, the diagnosis of AKI is still based on serum creatinine and urine output, which are not obvious in early AKI. It is difficult for clinicians to recognize AKI in time [12]. Early recognition and prevention of potential AKI is importance.

The traditional linear models require the statistical assumption of a liner relationship between the covariates and the risk of morbidity, and are often overfitting and multicollinearity. Machine learning approaches were introduced for better or comparable predictive ability than statistical analysis to predict postoperative outcomes. AI may offer opportunities for identifying patients at risk within a time window that enables early treatment [5]. On 9 June 2014, National Health Service (NHS) England published the national AKI algorithm in its patient safety alert, recommending “the wide scale introduction and uptake of an automated computer software algorithm to detect AKI” [13]. In 2015, Google developed the Streams program, which could predict AKI and send warnings to doctors to early intervention [13]. After that, the application of AI in AKI gradually attracted scientists' attention.

Tomaše et al. build a model which can predict 55.8% of all inpatient episodes of AKI, and 90.2% of all AKI that required subsequent administration of dialysis by AI in 703,782 adult patients [5]. Lee et al. [14] retrospectively reviewed 2,010 patients after cardiac surgery and used six machine learning techniques, including decision tree, random forest(RF), extreme gradient boosting, support vector machine(SVM), neural network classifier, and deep learning, to train AKI prediction models. The study demonstrated that the machine learning technique of extreme gradient boosting showed significantly better performance than the traditional logistic regression analysis or previous risk scores in predicting both AKI of all stages and stage 2 or 3 AKI after cardiac surgery which may help to evaluate the risk of AKI at the end of surgery. Yin et al.[15] retrospectively reviewed 8,800 patients undergoing contrast administration to develop the model for prediction of Contrast-induced nephropathy (CIN), the third cause of all hospital-acquired renal failure [16], by the machine learning method of RF. The model shown good predictive ability of CIN development and might provide preventative measures for CIN. Hamid et al. [17] used boosted ensembles of decision trees to train an AKI prediction tool on retrospective data taken from more than 300,000 inpatients. The prediction tool offered important predictive capability for detecting which patients were likely to suffer AKI. Prediction is improved for the cases with closer kinetics to AKI. These tools allow clinicians to potentially intervene before kidney damage manifests. Tang et al. [18] built risk prediction models for AKI in 157 severely burned patients, and compare the prediction performance of XGBoost machine learning and logistic regression model; machine learning method was found to have a better prediction performance than logistic regression. Besides, a Gradient Boosting Machine algorithm predicted serum creatinine-based Kidney Disease Improving Global Outcomes stage 2 AKI using electronic health record data for longitudinal use in 121,158 hospitalized patients. The algorithm had a sensitivity of 84% and a specificity of 85% for stage 2 AKI which the AUC (95% CI) was 0.90 (0.90-0.90) for predicting stage 2 AKI within 24 hours and 0.87 (0.87-0.87) within 48 hours. The AUC was 0.96 (0.96-0.96) for receipt of renal replacement therapy in the next 48 hours [19]. Another study demonstrated that machine learning models (multivariate logistic regression, RF and artificial neural networks (ANN)) can predict AKI onset following ICU admission in 23,950 patients with a competitive AUC (mean AUC 0.783) [20] (Table 1).

Alerting CKD

There are also reports of AI applications in alerting the occurrence of CKD. A pilot program using e-technologies to detect CKD was conducted in Australia (Electronic Diagnosis and Management Assistance to Primary Care in Chronic Kidney Disease; EMAP-CKD). The software was built on algorithms trained to identify at-risk patients and to order a relevant screening test for CKD [21].

In addition, AI has also been studied in the early warning of complications of CKD. Galloway et al. reported that using only 2 ECG leads, a deep-learning model detected hyperkalemia in patients with renal disease with an AUC of 0.853 to 0.883. The application of artificial intelligence to the ECG may enable screening for hyperkalemia of CKD patients. However, the study is retrospective and need prospective testing. Additionally,the model is a screening test with low specificity, with upwards of 42% false-positive results, which may cause anxiety and inconvenience for patients.[22]. Pilia et al. also use an artificial neural network to reconstruct the extracellular ionic concentrations for both potassium and calcium with an acceptable precision in CKD patients [23].

Besides, AI can also predict cost and mortality of patients. Lin et al. claimed that applying AI modeling could help to provide reliable information about one-year outcomes following dialysis in the aged and super-aged populations. They concluded that those with cancer, alcohol-related disease, stroke, chronic obstructive pulmonary disease (COPD), previous hip fracture, osteoporosis, dementia, and previous respiratory failure had higher medical costs and a high mortality rate [24].

Moreover, Eiichiro et al. identified factors of progressive CKD from healthy population at a health check point by using Bayesian network and artificial intelligence. They included hypertension, the time-series changes in the prognostic category of CKD, proteinuria and eGFR et al [25]. Besides, Almansour et al. compared the ANN and SVM techniques in a dataset of 400 patients to predict CKD in early stage. The empirical results from the experiments indicated that ANN performed better than SVM, with accuracies of 99.75% and 97.75%, respectively [26]. Chen Z et al. also used multivariate models, i.e., K-nearest neighbor (KNN), SVM, and soft independent modeling of class analogy (SIMCA), to evaluate risk of 386 patients to predict CKD. The overall accuracies were over 93% [27]. Bermudez-Lopez M et al. also used RF analysis to point out that new parameters such as Proprotein convertase subtilisin-kexin type (PCSK9) have a higher discrimination ability to classify patients into the non-diabetic CKD group [28].

The high morbidity rate associated with kidney stone disease is one of the main concerns in healthcare systems. Kazemi Y et al. developed a model for the early detection of the type of kidney stone and the most influential parameters in 936 patients with nephrolithiasis. The final ensemble-based model (with an accuracy of 97.1%) could be safely applied to predict the chances of developing nephrolithiasis [29].

Whereas, the current studies are mainly retrospective analyses, and the applicability needs further verification. Moreover, it is reported that an ANN model using 3 variables did not perform better than a new regression model in improving GFR estimation [30]. Furthermore, AI technologies face ethical and legal challenges yet to clarify. In 2016, DeepMind Technologies Limited, a wholly-owned subsidiary of the Google conglomerate, Alphabet Inc., announced its first major health project: a collaboration with the Royal Free London NHS Foundation Trust, to assist in the management of AKI. Initially received with great enthusiasm, the collaboration has suffered from a lack of clarity and openness, with issues of privacy and power emerging as potent challenges as the project has unfolded [13]. In the end, the project was halted due to a lack of privacy and consent to transferring population-derived dataset to large private prospectors [31].

Computer Aided Diagnosis--diagnostic assistance

Computer Aided Diagnosis (CAD) is a technology combined medical image and computer image processing to quantify and judge the characteristics of the focus, could assist clinicians to identify and analyze lesions timely and accurately [32]. The function of CAD has been verified in many aspects, especially in tumors, such as skin cancer, breast cancer, lung cancer, and so on[33]. The studies related to kidney disease are scanty, mainly about imaging diagnosis and pathological diagnosis.

Imaging diagnosis

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common hereditary disease in kidney. It is characterized by progressive enlargement of the kidneys caused by progressive development of renal cysts, often accompanied by declining renal function [34]. Total kidney volume (TKV) associated with renal function, is a crucial biomarker for studying progression of ADPKD. Traditional methods for TKV computation are based on stereology and manual segmentation for Computed Tomography (CT) and Magnetic Resonance Imaging. The accuracy of this method depends on user-specified parameters. It is significantly important to develop rapid and reliable methods for TKV quantification, CAD is a good choice. In 2017, Kanishka et al. [35] used an automated segmentation method based on deep learning for TKV computed on CT dataset of 244 ADPKD patients. The new method facilitates fast and reproducible diagnosis, and TKV measurements transmission agrees with manual segmentations from clinical experts. Similarly, Timothy et al. [36]used an automated method to segment the kidney and measure TKV from 2400 cases of MR images. The method simulated a multi-observer approach to create an accurate and robust method for segmentation and computation of TKV. However, CAD technology only could obtain a primary diagnosis. If some characteristics are not included in training database, they need to be judged by the clinician, after that they will be included in the training model to continue learning to improve the diagnostic ability. Most recently, van Gastel MDA et al. successfully developed a fully automated segmentation method for TKV measurement that uses a deep learning network in 540 abdominal magnetic resonance images (T2-weighted HASTE coronal sequences) from patients with ADPKD. TKV measured by the automated approach correlated highly with manually traced TKV (intraclass correlation coefficients, 0.998), with low bias and high precision (<0.1%±2.7% for TKV) [37].

It is often difficult for physicians to achieve preoperative differential diagnosis between renal cell carcinoma and some benign renal tumors by virtue of existing imaging techniques (including CT and MRI), such as adiposity angiomyolipoma [38].In most cases, such benign tumors only require conservative treatment or follow-up, so it is particularly important to achieve accurate preoperative diagnosis of renal cell carcinoma and renal benign tumors[39]. Automatic deep feature classification (DFC) method can distinguished both benign angiomyolipoma without visible fat (AMLwvf)[40, 41] and oncocytoma[42] from malignant renal cell carcinoma (ccRCC) from abdominal computer tomography (CT) images.

Besides, Image genomics can complete genomic analysis in characterizing disease biology by extracting a large number of tumor image features through AI, and associating the image features with the underlying mutation status of tumors, molecular markers, underlying activated biologic pathways, or clinical outcomes by developing “association maps” between them [43, 44]. Jamshidi et al. constructed an alternative model for multi-gene expression molecular detection of renal clear cell carcinoma based on image genomics by using CT imaging features, thus achieving the independent prediction of disease-related survival of patients without any invasion method [45]. It is found out that the associations between tumor angiogenesis and radiomic imaging features from PET/MRI, which can predict the prognostic and guide the treatment of antiangiogenic agents of clear cell renal cell carcinoma (ccRCC) [46, 47]. However, most of the current clinical studies are single-center studies with small sample size, and lacking cross-test and verification.

What is more, Kuo et al. identified the CKD status defined by an eGFR of <60 ml/min/1.73 m2 based on 4,505 kidney ultrasound images by deep neural network (The AUC of the model is 0.904). A Pearson correlation coefficient of 0.741 and accuracy of 85.6% indicated the strong relationship between AI and creatinine-based GFR estimations [48].

Congenital abnormalities of the kidney and urinary tract (CAKUT) in children are a challenging task. A pre-trained deep learning model (imagenet-caffe-alex) is adopted for transfer learning-based feature extraction from 3-channel feature maps computed from ultrasound images. SVM classifiers are then built upon different sets of features, including the transfer learning features, conventional imaging features, and their combination. The AUC for classifiers built on the combination features were 0.92, 0.88, and 0.92 for discriminating the left, right, and bilateral abnormal kidney scans from controls with classification rates of 84%, 81%, and 87%; specificity of 84%, 74%, and 88%; and sensitivity of 85%, 88%, and 86%, respectively. It is suggested that the combination of transfer learning features and conventional imaging features yielded the best classification performance for distinguishing CAKUT patients from normal controls based on their ultrasound kidney images [49, 50].

Pathological diagnosis

Renal interstitial fibrosis is an indicator of the presence and extent of chronic kidney disease. The standard quantitative method of visual evaluation is very important for the diagnosis of renal diseases. The Banff schema is one of the standards used for the renal allograft rejection grades classification. The visual scoring is subject to pathologists' intra- and inter-observer variability, may not be repeatable or reproducible. CAD can reduce the workload of pathologists, also has an advantage of precision and meticulousness. Wei et al.[51] developed an automated quantification system for measuring the interstitial fibrosis in 40-image and use 70 kidney patients to prove the error rate. It had shown an average error of 9%. The system demonstrated to be an effective quantification system as a diagnostic aide. Kannan et al. developed a deep learning framework to accurately identify and segment glomeruli from digitized images of human kidney biopsies. The segmentation model that was based on the convolutional neural network (CNN) multilabel classifier accurately marked the globally sclerosis glomeruli on the test data, which indicated the power of deep learning for assessing complex histologic structures from digitized human kidney biopsies [52]. Vijaya B Kolachalama et al. also leveraged a deep learning architecture to better associate patient-specific histologic images with clinical phenotypes (training classes) including CKD stage, serum creatinine, and nephrotic-range proteinuria at the time of biopsy, and 1-, 3-, and 5-year renal survival in 171 patients. AUC values for the CNN models in predicting creatinine, proteinuria and 1-, 3-, and 5-year renal survival were 0.912, 0.867, 0.878, 0.875, and 0.904 [53]. Li C et al. trained a RF algorithm in 222 patients to build a pathological prediction model of primary nephrotic syndrome (accuracy 62.2%) [54]. However, the specimen number was small, and the general applicability was uncertain, more researches were needed to improve in the future.

Make appropriate ICD Codes

International Classification of Disease (ICD) codes is important for population health and cohort discovery when clinical information is limited. Sina Rashidian et al. used deep learning methods which based on demographics, lab results, and medications, as well as codes from previous encounters to model coder decision making. Three test cases were investigated including acute renal failure (ARF) and CKD, the AUC of predicting ARF and CKD were 0.9194 and 0.9424 separately[55].

Guiding treatment

Guidelines are the basis for decision-making, which are formulated through large-scale investigations. These guidelines are thus population-based and adjustments are needed using the guidelines on individual cases. Personalized and accurate treatment protocols are required. AI can analyze the association of treatment protocols and efficacy from a large number of patients, develop models based on efficacy and risk factors, guide the choice of treatment protocols, and improve clinical efficacy. Related studies on kidney disease are scanty, mainly in hemodialysis patients.

Anemia treatment

Anemia is one of the main common comorbidities in patients undergoing hemodialysis. The incidence and severity of anemia are gradually increasing as renal function declining [56]. In 2016, China Dialysis Outcomes and Practice Patterns Study (China's DOPPS) showed the prevalence of anemia in CKD being 21% [57]. Anemia can increase the proportion of left ventricular hypertrophy, cause heart failure and myocardial infarction, reduce quality of life and increase the risk of death. Treatment costs and mortality were also significantly increased by anemia [58]. The major cause of anemia in CKD is deficiency in erythropoietin (EPO) production [59]. Erythropoietin stimulating agents (ESAs), which would supplement EPO and increase hemoglobin (Hb) level, are widely applied by clinicians. However, the toxicities of ESAs have been verified. ESAs would increase the incidence of cardiovascular events, tumor progression, and mortality [60, 61]. It was reported that the toxicities are associated with dose [62]. It is important to find an adequate treatment for every patient in each particular situation.

Substantial progress has been made in the application of computer-driven methods to provide erythropoietic dosing information for patients with anemia resulting from chronic kidney disease. Initial solutions were simply computerized versions of traditional paper-based anemia management protocols. True personalization was achieved through the use of advanced modeling techniques such as artificial neural networks, physiologic models, and feedback control systems [63]. Early in 2003, experts in Spain have carried out an individualized prediction of the EPO dosage to be administered to CKD patients and successfully aided in the individualization of dosage and provided state-of-the-art regression models to clinicians [64] in a single center. In 2008, Gaweda et al. also reported that model predictive control (MPC) by using an artificial neural network model of EPO may result in improved anemia management [65]. Both studies had relatively small sample sizes. In 2014, Carlo used Machine Learning (Multilayer Perceptron, MLP) and linear model, which were built for prediction of ESAs therapy response, to recommend suitable ESAs doses. The accuracy of MLP prediction model was more than 90%. The MLP model outperforms previous approaches of the Hb prediction [66]. To evaluate the impact of the model, the team conducted a 24-month retrospective study using additional 752 hemodialysis patients in 2016. It was reported that median ESAs consumption decreased and on-target Hb values increased based on the model suggestions. Moreover, Hb fluctuation had a significant decrease. The model could help to improve anemia outcomes of patients with hemodialysis, minimizing ESAs dose with the potential to reduce treatment cost [67]. In 2018, María et al. [68] also assessed the usefulness of this model. The model could help to increase the percentage of Hb in range and reduce the intake of ESAs with less Hb fluctuations. Meanwhile, the transfusion, hospitalization and cardiovascular events were all decreased. In conclusion, the model was an effective tool to help clinicians to minimize the risks of treatment with ESAs and reduce costs. However, the sample size was not very large and the follow-up time was insufficient to assess the impact of the model on cardiovascular morbidity and mortality. At that time, the model has only used for hemodialysis patients, more trials should be carried out to verify the usefulness of anemia treatment in pre-dialysis and peritoneal dialysis patients. Moreover, these approaches are data-intensive and typically perform well in ranges in which adequate data exist to model the ESA response, but are unable to extrapolate beyond these ranges [63].

Blood pressure and fluid volume management

Blood pressure (BP) and fluid volume are crucial points for patients undergoing hemodialysis. The prevalence of hypertension is 40-90% of patients with ESRD according to the BP definition used, the population selected, and the timing of measurement [69, 70]. Clinicians often reduce extracellular fluid volume overload to control BP, which would increase the incidence of intradialytic hypotension. Both intradialytic hypotension and chronic hypertension are associated with poor prognosis. The clinical system EuCliD® is an international electronic health record repository allowing point-of-care data collection of routine clinical practice information [71]. By exploiting such wealth of information, Carlo et al. [71] developed a multiple-endpoint model predicting session-specific Kt/V, fluid volume removal, heart rate, and BP based on 766,000 records in 2019. The accuracy and precision of the model is encouraging. The model may help to make the optimized decision in multidimensional other than currently limited single-endpoint treatment strategies.

 Figure 1 

Artificial intelligence involves the science and engineering for developing smart wearable artificial kidneys ^[72]

Wearable dialysis devices

Dialysis is the main treatment for ESRD. Dialysis affects the patient's life in a wide range, and some patients cannot tolerate hemodynamic instability of intermittent dialysis, there are great expectations for the development of wearable artificial kidneys. Wearable dialysis devices can make the real-time analysis of equipment alarms, dialysis parameters, and patient-related data with a real-time feedback response. Martin et al. [72] combined AI and regenerative medicine technology to develop wearable dialysis devices. These devices can conduct continuous dialysis, remove toxins effectively and have little effect on hemodynamic (Figure 1). The devices have been tested in 15 ESRD patients. The results showed that dialysis was effective without any adverse reactions. The devices were authorized as a breakthrough device by the America Food and Drug Administration. However, the sample size is small; more researches are needed to include more patients to improve the model in the future. Another interesting approach is the wearable artificial kidney, a 5-kg wearable, miniaturized device with a sorbent-based hemodialysis system that is worn on the waist like a toolkit belt and is currently under development at the University of Washington, USA. An exploratory clinical trial with 10 patients received therapy with a wearable artificial kidney for 24 h. However, the trial was stopped after the inclusion of the 7th subject because of device-related technical problems, including an excessive presence of carbon dioxide bubbles in the dialysate circuit, which exceeded its degassing capacity; tubing kinks; and variable pump function that resulted in fluctuating blood and dialysate flow rates [73]. Another remarkable innovation is the implantable Renal Assist Device (iRAD) that uses micromachining techniques to fabricate a biohybrid system able to mimic renal morphology and function. This artificial kidney is a bionic device that incorporates a silicon nanopore membrane and a bioreactor of live kidney cells that will concentrate the ultrafiltrate into urine. The bundle is enclosed in a body-friendly box and connected to a patient's circulatory system and bladder. Despite having been used with success in animal models [74], it is still under development to scale it up to the clinical environment [75]. Recently, experts found MXene Sorbents for Removal of Urea from Dialysate, which open a new opportunity in designing a miniaturized dialysate regeneration system for a wearable artificial kidney [76].

Assistance of needle insertion

Robotics are also steadily being introduced in health care, especially in surgery, with systems such as the da Vinci® Surgical System that involves a magnified 3D high-definition computer vision system (part of it aided by ML) and tiny wristed instruments that bend and rotate more complexly than the human hand. An autonomous image-guided robotic needle insertion for blood draws and intravenous insertions has also been designed that combines robotics, AI, computer vision, and image technology (Figure 2) [77]. It must be made clear that a dialysis machine is not an AI-guided robot, since it is not able to respond to its environments in ways that humans have not explicitly taught it to. However, it is easy to imagine future dialysis robots capable of carrying out complex series of actions automatically or in a semi-autonomous fashion. Besides, it is reported that accurate needle insertion (< 3 mm error) can be achieved in common target sites including the kidneys when using a CT-guided robotic system [78]. The proposed optical tracker based robot registration and serving method is capable of accurate three dimension needle operation for ultrasound-guided percutaneous renal access (PRA) procedure with improved precision and shortened time [79].

Evaluating prognosis

AI can identify factors affecting prognosis by analyzing database, and develop models evaluating the relationship between factors and prognosis. In this section, we will summarize AI applications in evaluating prognosis involving several common kidney diseases.

Chronic Kidney Disease Mineral and Bone Metabolism Disorders (CKD-MBD)

CKD-MBD is another common comorbidity in ESRD patients, which increases mortality. The serum concentrations of phosphate (P), calcium (Ca) or parathyroid hormone (PTH) are associated with negative outcomes. The three parameters, P, Ca, PTH, interplay of each other, but the relationship is non-linear. Classical statistical methods have no advantages on analyzing associations among variables non-linear but affected by non-trivial feedback loops. The machine learning seems to be a predictive analytic approach. To quantify the degree of association between the three parameters, Mariano et al developed a data analysis system by RF from 1,758 HD patients. Comparing with Classical statistical methods, the power of prediction of the new model was markedly increased [80]. In 2018, Kleiman et al.[81] used RF algorithms to build model predicting risks for development of calciphylaxis in CKD patients.With an AUC value of 0.872, the model could successfully predict calciphylaxis, provide an opportunity for clinical translation of the predictive models.

 Figure 2 

System design and architecture for automated cannula insertion. (a) Functional prototype. (b) Major functional components. (c) Device data flow.(d) Hardware architecture grouped by function ^[77].

IgA nephropathy (IgAN)

IgAN is the most common primary glomerular kidney disease. About 20-40% of IgAN patients will reach ESRD within 10-20 years of diagnosis. Early prediction of ESRD is valuable. Liu et al. [82] retrospectively reviewed 262 biopsy-proven IgAN patients, and employed artificial intelligence to predict the ESRD status in IgAN patients. The predictive model showed that Oxford-MEST scores, C3 staining and eGFR were important role for ESRD prediction in Chinese IgAN patients. Most recently, Chen et al. [83] developed a prediction model using routinely available characteristics (demographic, clinical, and pathologic variables) and based on the combination of a machine learning algorithm and survival analysis which can stratify risk for kidney disease progression in the setting of IgAN.

Diabetic Kidney Disease (DKD)

DKD is a common complication and a mainly cause of diabetes deaths. It is critical to identify the risk factors to stratify DKD risk to improve patient management. As early in 2013, Leung RK et al. used a multi-staged strategy based on machine learning and mathematical modeling to predict genotype-phenotype risk patterns in 119 DKD patients and 554 without DKD type 2 diabetic patients. They found out that age, age of diagnosis and lipid parameters were major clinical predictors while genetic polymorphisms related to inflammation and lipid metabolism were the most selected genetic predictors [84].

In 2018, Arianna et al. [85] used machine learning to set a predictive of type 2 diabetes mellitus complications from 1000 patients with type 2 diabetes. The Random Forest model had the highest predictive performance. The model showed that variables, such as gender, age, time from diagnosis, body mass index, glycated hemoglobin, hypertension, and smoking habit, contributed more than others. The accuracy of the model was 0.838, more studies should be conduct to improve the accuracy and sensitivity. Another research also claimed that machine learning could compare frequent medical problems of African American and Caucasian Diabetic Kidney disease in 4,623 diabetic patients. This study found that African Americans have much higher rates of CKD-related medical problems than Caucasians for all five CKD stages, and prominent markers leading to ESRD were high glucose, high systolic BP, obesity, alcohol/drug use, and low hematocrit. In 2019, Ravizza et al. [86] carried out a direct comparison of algorithms derived from real-world data (RWD) and clinical data for quantifying the risk of CKD as a long-term complication of diabetes. After teaching the Roche/IBM model using seven prioritized features, including age, body mass index, and glomerular filtration rate, creatinine, albumin, glucose, and hemoglobin, the AUC of the prediction algorithm was 0.7937. It is concluded that the teaching of predictive analytics algorithms using real-world data could achieve equivalent or even enhanced accuracy compared with those using clinical trial data. Most recently, Song X et al. presented an ensemble feature selection approach to identify a robust set of discriminant factors to predict DKD in 15,645 adult patients with type 2 diabetes [87]. The ensemble model identified a set of 440 features, including 191 labs, 51 visit details (mainly vital signs), 39 medications, 34 orders, 30 diagnoses, and 95 other clinical features with an AUC of 0.82 on internal validation and 0.71 on external temporal validation. Besides, Makino et al. also constructed a new predictive model for DKD using AI based on the EMR of 64,059 diabetes patients. AI could predict DKD aggravation with 71% accuracy (the resultant average of the AUC was 0.743) which may contribute to more effective and accurate intervention to reduce hemodialysis [88].

Kidney transplantation

Kidney transplantation is another main treatment for ESRD. But only a few patients can receive kidney transplantation because the shortage of kidney and high technical requirements. Predicting the outcome of kidney transplantation is important to optimize transplantation parameters and modify factors related to recipient, donor, and transplant procedure. Lofaro et al. [89] retrospectively analyzed 80 renal transplant patients with 5-year follow-up, using classification trees to develop two predictive models and identifying six variables that contributed high on patient outcomes. The AUC values of these two models are 0.847 and 0.824 respectively. In another study, 4754 systemic lupus erythematosus patients who underwent kidney transplantation were enrolled. Predictive models were developed by 3 machine learning algorithm. The AUC of ANN (0.73) based on six variables was slightly better than the logistic regression based on six variables selected by Weka (0.73) and classification trees (0.70). The study showed that the ANN model had better predictive performance than other models [90]. Abdeltawab H et al. also developed a deep-learning based CAD system based on the fusion of both imaging markers and clinical biomarkers for the early detection of acute renal transplant rejection. The overall accuracy of the proposed system is 92.9% with 93.3% sensitivity and 92.3% specificity in distinguishing non-rejected kidney transplants from rejected ones [91].

CKD after AKI

Several studies between 2008 and 2017 have demonstrated that although acute kidney injury is usually reversible, some patients may experience incomplete recovery of kidney function, while others subsequently develop accelerated loss of kidney function, resulting in an increased risk of chronic kidney disease [92-94]. A prediction of advanced CKD following hospitalization with AKI will result in got opportunities to intervene and potentially improve long-term outcomes and avoid unnecessary use of clinical resources [95, 96]. A multivariable model was developed with 9973 participants and was externally validated with 2761 participants to develop a practical risk stratification approach that could be used to identify patients at high risk of chronic kidney disease after they are discharged. This model using routine laboratory data was able to predict advanced chronic kidney disease following hospitalization with acute kidney injury. But requires evaluation of its utility in a clinical setting [97].

CKD severity

Norouzi et al. predicted renal failure progression in 465 CKD patients by using Integrated Intelligent Fuzzy Expert System and found out that the model could accurately (>95%) predict the GFR for sequential 6-, 12-, and 18-month intervals [98]. Xiao et al. compared nine predictive models, including logistic regression, Elastic Net, lasso regression, ridge regression, SVM, RF, XGBoost, neural network and k-nearest neighbor in prediction of CKD progression in 551 patients with proteinuria (The AUC values of the 9 models were 0.873, 0.871, 0.872, 0.865, 0.857, 0.854, 0.868, 0.854, 0.802, respectively). The study showed that the model with the highest sensitivity was Elastic Net (0.85), while XGBoost showed the highest specificity (0.83). ALB, Scr, TG, LDL and eGFR levels, showed predictive ability for CKD severity [99]. Moreover, Zacharias HU et al. identified CKD patients at risk of progressing to ESRD in 4,640 patients by state-of-the-art machine learning methods. The results demonstrated that proton nuclear magnetic resonance features, such as creatinine, high-density lipoprotein, valine, acetyl groups of glycoproteins, and Ca²⁺-EDTA carried the highest weights are predicting factors [100].

Death Risk, cardiovascular risk after dialysis

The study was carried out on a contemporary cohort of 27,615 US veterans with incident ESRD by implementing a random forest method on 49 variables obtained before dialysis transition to predict outcomes of 30-, 90-, 180-, and 365-day all-cause mortality after dialysis initiation. The results showed that the model provided C-statistics (95% CI) of 0.7185 (0.6994-0.7377), 0.7446 (0.7346-0.7546), 0.7504 (0.7425-0.7583), and 0.7488 (0.7421-0.7554) for predicting risk of death within the 4 different time windows [101]. Mezzatesta S et al. used non-linear SVC with RBF kernel algorithm, optimized with GridSearch, allowed to obtain an accuracy of 95.25% in the Italian dataset and of 92.15% in the American dataset, in the prediction of Ischaemic Heart Disease in patients on dialysis [102].

Summary

It is noticeable that AI does not only play great role in Nephrology (Figure 3), but also in many other disciplines. Take Urology as an example, AI is applied for the prediction of genitourinary cancers [103]. We are witnessing the development of medical practice from empirical medicine to evidence-based medicine to intelligent diagnosis and to AI-directed medicine. While AI medicine is still in its infant stage, it is no question that by taking advantage of the diversity and complexity of the real-world data, AI will produce prediction algorithms suitable for routine clinical application in the near future. These findings may fuel a fundamental discussion of future medical evidence beyond the exploration of original targets for analyzing and interpreting data that are potentially costly, long-term clinical trials with a limited number of patients that may one day enhance, or even partially replace, real-world data-driven risk assessments [86]. In the future, AI is increasingly important in clinic, which can make clinician work efficiency and alleviate the pressure. Nonetheless, AI is facing multiple challenges, including the data quality uneven, lacking of agreed standards of different center, lacking of scientific verification, and the security, privacy of data. At the same time, the current studies are major retrospective studies, and absent large multi-center studies. More research is needed to apply AI to kidney diseases.

Acknowledgements

This work was supported in part by the Hunan Provincial Key Research and Development Plan under Grant no. 2018WK2061 and Xiangya Clinical Big Data Project of Central South University.

Competing Interests

The authors have declared that no competing interest exists.

 Figure 3 

AI applications in kidney disease in alerting systems, diagnostic assistance, guiding treatment and evaluating prognosis. AKI, acute kidney disease. CKD, chronic kidney disease. CKD-MBD, Chronic Kidney Disease - Mineral and Bone Disorder. IgAN, IgA nephropathy.

References

1. GBD 2015 DALYs and HALE Collaborators. Global, regional, and national disability-adjusted life-years (DALYs) for 315 diseases and injuries and healthy life expectancy (HALE), 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet (London, England). 2016;388:1603-58

2. Kim SH, Jo MW, Go DS, Ryu DR, Park J. Economic burden of chronic kidney disease in Korea using national sample cohort. J Nephrol. 2017;30:787-93

3. Fleming N. How artificial intelligence is changing drug discovery. Nature. 2018;557:S55-S7

4. Yu ZG. Artificial Intelligence and Medical. Academic Journal of Second Military Medical University. 2018;39(8):1

5. Tomašev N, Glorot X, Rae JW, Zielinski M, Askham H, Saraiva A. et al. A clinically applicable approach to continuous prediction of future acute kidney injury. Nature. 2019;572:116-9

6. Sanchez-Pinto LN, Venable LR, Fahrenbach J, Churpek MM. Comparison of variable selection methods for clinical predictive modeling. Int J Med Inform. 2018;116:10-7

7. Lewington AJ, Cerdá J, Mehta RL. Raising awareness of acute kidney injury: a global perspective of a silent killer. Kidney Int. 2013;84:457-67

8. Waikar SS, Curhan GC, Wald R, McCarthy EP, Chertow GM. Declining mortality in patients with acute renal failure, 1988 to 2002. J Am Soc Nephrol. 2006;17:1143-50

9. Silver SA, Long J, Zheng Y, Chertow GM. Cost of Acute Kidney Injury in Hospitalized Patients. J Hosp Med. 2017;12:70-6

10. Chawla LS, Eggers PW, Star RA, Kimmel PL. Acute kidney injury and chronic kidney disease as interconnected syndromes. N Engl J Med. 2014;371:58-66

11. Li PK, Burdmann EA, Mehta RL. Acute kidney injury: global health alert. Kidney Int. 2013;83:372-6

12. Huang C, Murugiah K, Mahajan S, Li SX, Dhruva SS, Haimovich JS. et al. Enhancing the prediction of acute kidney injury risk after percutaneous coronary intervention using machine learning techniques: A retrospective cohort study. PLoS Med. 2018;15:e1002703

13. Powles J, Hodson H. Google DeepMind and healthcare in an age of algorithms. Health Technol (Berl). 2017;7:351-67

14. Lee HC, Yoon HK, Nam K, Cho YJ, Kim TK, Kim WH. et al. Derivation and Validation of Machine Learning Approaches to Predict Acute Kidney Injury after Cardiac Surgery. J Clin Med. 2018;7:E322

15. Yin WJ, Yi YH, Guan XF, Zhou LY, Wang JL, Li DY. et al. Preprocedural Prediction Model for Contrast-Induced Nephropathy Patients. J Am Heart Assoc. 2017 6

16. Nash K, Hafeez A, Hou S. Hospital-acquired renal insufficiency. Am J Kidney Dis. 2002;39:930-6

17. Mohamadlou H, Lynn-Palevsky A, Barton C, Chettipally U, Shieh L, Calvert J. et al. Prediction of Acute Kidney Injury With a Machine Learning Algorithm Using Electronic Health Record Data. Can J Kidney Health Dis. 2018;5:2054358118776326

18. Tang CQ, Li JQ, Xu DY, Liu XB, Hou WJ, Lyu KY. et al. Comparison of machine learning method and logistic regression model in prediction of acute kidney injury in severely burned patients. Chin J Burns. 2018;34:343-8

19. Koyner JL, Carey KA, Edelson DP, Churpek MM. The Development of a Machine Learning Inpatient Acute Kidney Injury Prediction Model. Crit Care Med. 2018;46:1070-7

20. Zimmerman LP, Reyfman PA, Smith ADR, Zeng Z, Kho A, Sanchez-Pinto LN. et al. Early prediction of acute kidney injury following ICU admission using a multivariate panel of physiological measurements. BMC Med Inform Decis Mak. 2019;19:16

21. Shah H. The DeepMind debacle demands dialogue on data. Nature. 2017;547:259

22. Galloway CD, Valys AV, Shreibati JB, Treiman DL, Petterson FL, Gundotra VP. et al. Development and Validation of a Deep-Learning Model to Screen for Hyperkalemia From the Electrocardiogram. JAMA Cardiol. 2019;4:428-36

23. Pilia N, Mesa MH, Dossel O, Loewe A. ECG-based Estimation of Potassium and Calcium Concentrations: Proof of Concept with Simulated Data. Conf Proc IEEE Eng Med Biol Soc. 2019;2019:2610-3

24. Lin SY, Hsieh MH, Lin CL, Hsieh MJ, Hsu WH, Lin CC. et al. Artificial Intelligence Prediction Model for the Cost and Mortality of Renal Replacement Therapy in Aged and Super-Aged Populations in Taiwan. J Clin Med. 2019 8

25. Kanda E, Kanno Y, Katsukawa F. Identifying progressive CKD from healthy population using Bayesian network and artificial intelligence: A worksite-based cohort study. Sci Rep. 2019;9:5082

26. Almansour NA, Syed HF, Khayat NR, Altheeb RK, Juri RE, Alhiyafi J. et al. Neural network and support vector machine for the prediction of chronic kidney disease: A comparative study. Comput Biol Med. 2019;109:101-11

27. Chen Z, Zhang X, Zhang Z. Clinical risk assessment of patients with chronic kidney disease by using clinical data and multivariate models. Int Urol Nephrol. 2016;48:2069-75

28. Bermudez-Lopez M, Forne C, Amigo N, Bozic M, Arroyo D, Bretones T. et al. An in-depth analysis shows a hidden atherogenic lipoprotein profile in non-diabetic chronic kidney disease patients. Expert Opin Ther Targets. 2019;23:619-30

29. Kazemi Y, Mirroshandel SA. A novel method for predicting kidney stone type using ensemble learning. Artif Intell Med. 2018;84:117-26

30. Liu X, Li NS, Lv LS, Huang JH, Tang H, Chen JX. et al. A comparison of the performances of an artificial neural network and a regression model for GFR estimation. Am J Kidney Dis. 2013;62:1109-15

31. Møllersen K, Kirchesch H, Zortea M, Schopf TR, Hindberg K, Godtliebsen F. Computer-Aided Decision Support for Melanoma Detection Applied on Melanocytic and Nonmelanocytic Skin Lesions: A Comparison of Two Systems Based on Automatic Analysis of Dermoscopic Images. Biomed Res Int. 2015;2015:579282

32. Venuthurupalli SK, Hoy WE, Healy HG, Cameron A, Fassett RG. CKD Screening and Surveillance in Australia: Past, Present, and Future. Kidney Int Rep. 2018;3:36-46

33. Esteva A, Kuprel B, Novoa RA, Ko J, Swetter SM, Blau HM. et al. Dermatologist-level classification of skin cancer with deep neural networks. Nature. 2017;542:115-8

34. Grantham JJ. The etiology, pathogenesis, and treatment of autosomal dominant polycystic kidney disease: recent advances. Am J Kidney Dis. 1996;28:788-803

35. Sharma K, Rupprecht C, Caroli A, Aparicio MC, Remuzzi A, Baust M. et al. Automatic Segmentation of Kidneys using Deep Learning for Total Kidney Volume Quantification in Autosomal Dominant Polycystic Kidney Disease. Sci Rep. 2017;7:2049

36. Kline TL, Korfiatis P, Edwards ME, Blais JD, Czerwiec FS, Harris PC. et al. Performance of an Artificial Multi-observer Deep Neural Network for Fully Automated Segmentation of Polycystic Kidneys. J Digit Imaging. 2017;30:442-8

37. van Gastel MDA, Edwards ME, Torres VE, Erickson BJ, Gansevoort RT, Kline TL. Automatic Measurement of Kidney and Liver Volumes from MR Images of Patients Affected by Autosomal Dominant Polycystic Kidney Disease. J Am Soc Nephrol. 2019;30:1514-22

38. Lopes Vendrami C, Parada Villavicencio C, DeJulio TJ, Chatterjee A, Casalino DD, Horowitz JM. et al. Differentiation of Solid Renal Tumors with Multiparametric MR Imaging. Radiographics. 2017;37:2026-42

39. Soulen MC. Small Renal Masses: Challenges for the Radiologist. Radiology. 2018;288:91-2

40. Feng Z, Rong P, Cao P, Zhou Q, Zhu W, Yan Z. et al. Machine learning-based quantitative texture analysis of CT images of small renal masses: Differentiation of angiomyolipoma without visible fat from renal cell carcinoma. Eur Radiol. 2018;28:1625-33

41. Lee H, Hong H, Kim J, Jung DC. Deep feature classification of angiomyolipoma without visible fat and renal cell carcinoma in abdominal contrast-enhanced CT images with texture image patches and hand-crafted feature concatenation. Med Phys. 2018;45:1550-61

42. Yu H, Scalera J, Khalid M, Touret AS, Bloch N, Li B. et al. Texture analysis as a radiomic marker for differentiating renal tumors. Abdom Radiol (NY). 2017;42:2470-8

43. Shinagare AB, Krajewski KM, Braschi-Amirfarzan M, Ramaiya NH. Advanced Renal Cell Carcinoma: Role of the Radiologist in the Era of Precision Medicine. Radiology. 2017;284:333-51

44. Kuo MD, Jamshidi N. Behind the numbers: Decoding molecular phenotypes with radiogenomics-guiding principles and technical considerations. Radiology. 2014;270:320-5

45. Jamshidi N, Jonasch E, Zapala M, Korn RL, Aganovic L, Zhao H. et al. The Radiogenomic Risk Score: Construction of a Prognostic Quantitative, Noninvasive Image-based Molecular Assay for Renal Cell Carcinoma. Radiology. 2015;277:114-23

46. Yin Q, Hung SC, Wang L, Lin W, Fielding JR, Rathmell WK. et al. Associations between Tumor Vascularity, Vascular Endothelial Growth Factor Expression and PET/MRI Radiomic Signatures in Primary Clear-Cell-Renal-Cell-Carcinoma: Proof-of-Concept Study. Sci Rep. 2017;7:43356

47. Antunes J, Viswanath S, Rusu M, Valls L, Hoimes C, Avril N. et al. Radiomics Analysis on FLT-PET/MRI for Characterization of Early Treatment Response in Renal Cell Carcinoma: A Proof-of-Concept Study. Transl Oncol. 2016;9:155-62

48. Kuo CC, Chang CM, Liu KT, Lin WK, Chiang HY, Chung CW. et al. Automation of the kidney function prediction and classification through ultrasound-based kidney imaging using deep learning. NPJ Digit Med. 2019;2:29

49. Zheng Q, Furth SL, Tasian GE, Fan Y. Computer-aided diagnosis of congenital abnormalities of the kidney and urinary tract in children based on ultrasound imaging data by integrating texture image features and deep transfer learning image features. J Pediatr Urol. 2019;15:75.e1-e7

50. Zheng Q, Tasian G, Fan Y. TRANSFER LEARNING FOR DIAGNOSIS OF CONGENITAL ABNORMALITIES OF THE KIDNEY AND URINARY TRACT IN CHILDREN BASED ON ULTRASOUND IMAGING DATA. Proc IEEE Int Symp Biomed Imaging. 2018;2018:1487-90

51. Tey WK, Kuang YC, Ooi MP, Khoo JJ. Automated quantification of renal interstitial fibrosis for computer-aided diagnosis: A comprehensive tissue structure segmentation method. Comput Methods Programs Biomed. 2018;155:109-20

52. Kannan S, Morgan LA, Liang B, Cheung MG, Lin CQ, Mun D. et al. Segmentation of Glomeruli Within Trichrome Images Using Deep Learning. Kidney Int Rep. 2019;4:955-62

53. Kolachalama VB, Singh P, Lin CQ, Mun D, Belghasem ME, Henderson JM. et al. Association of Pathological Fibrosis With Renal Survival Using Deep Neural Networks. Kidney Int Rep. 2018;3:464-75

54. Li C, Yao Z, Zhu M, Lu B, Xu H. Biopsy-Free Prediction of Pathologic Type of Primary Nephrotic Syndrome Using a Machine Learning Algorithm. Kidney Blood Press Res. 2017;42:1045-52

55. Rashidian S, Hajagos J, Moffitt RA, Wang F, Noel KM, Gupta RR. et al. Deep Learning on Electronic Health Records to Improve Disease Coding Accuracy. AMIA Jt Summits Transl Sci Proc. 2019;2019:620-9

56. Stauffer ME, Fan T. Prevalence of anemia in chronic kidney disease in the United States. PloS one. 2014;9:e84943

57. Zuo L, Wang M, Hou F, Yan Y, Chen N, Qian J. et al. Anemia Management in the China Dialysis Outcomes and Practice Patterns Study. Blood Purif. 2016;42:33-43

58. Prasad-Reddy L, Isaacs D, Kantorovich A. Considerations and controversies in managing chronic kidney disease: An update. Am J Health Syst Pharm. 2017;74:795-810

59. Artunc F, Risler T. Serum erythropoietin concentrations and responses to anaemia in patients with or without chronic kidney disease. Nephrol Dial Transplant. 2007;22:2900-8

60. Coyne DW. Anemia in chronic kidney disease treating the numbers, not the patients. JAMA Intern Med. 2014;174:708-9

61. Pfeffer MA, Burdmann EA, Chen CY, Cooper ME, de Zeeuw D, Eckardt KU. et al. A trial of darbepoetin alfa in type 2 diabetes and chronic kidney disease. N Engl J Med. 2009;361:2019-32

62. Phrommintikul A, Haas SJ, Elsik M, Krum H. Mortality and target haemoglobin concentrations in anaemic patients with chronic kidney disease treated with erythropoietin: a meta-analysis. Lancet. 2007;369:381-8

63. Brier ME, Gaweda AE, Aronoff GR. Personalized Anemia Management and Precision Medicine in ESA and Iron Pharmacology in End-Stage Kidney Disease. Semin Nephrol. 2018;38:410-7

64. Martín-Guerrero JD, Camps-Valls G, Soria-Olivas E, Serrano-López AJ, Pérez-Ruixo JJ, Jiménez-Torres NV. Dosage individualization of erythropoietin using a profile-dependent support vector regression. IEEE Trans Biomed Eng. 2003;50:1136-42

65. Gaweda AE, Jacobs AA, Aronoff GR, Brier ME. Model predictive control of erythropoietin administration in the anemia of ESRD. Am J Kidney Dis. 2008;51:71-9

66. Barbieri C, Mari F, Stopper A, Gatti E, Escandell-Montero P, Martínez-Martínez JM. et al. A new machine learning approach for predicting the response to anemia treatment in a large cohort of End Stage Renal Disease patients undergoing dialysis. Comput Biol Med. 2015;61:56-61

67. Barbieri C, Molina M, Ponce P, Tothova M, Cattinelli I, Ion Titapiccolo J. et al. An international observational study suggests that artificial intelligence for clinical decision support optimizes anemia management in hemodialysis patients. Kidney Int. 2016;90:422-9

68. Bucalo ML, Barbieri C, Roca S, Ion Titapiccolo J, Ros Romero MS, Ramos R. et al. The anaemia control model: Does it help nephrologists in therapeutic decision-making in the management of anaemia?. Nefrologia. 2018;38:491-502

69. Agarwal R, Nissenson AR, Batlle D, Coyne DW, Trout JR, Warnock DG. Prevalence, treatment, and control of hypertension in chronic hemodialysis patients in the United States. Am J Med. 2003;115:291-7

70. Salem MM. Hypertension in the hemodialysis population: a survey of 649 patients. Am J Kidney Dis. 1995;26:461-8

71. Barbieri C, Cattinelli I, Neri L, Mari F, Ramos R, Brancaccio D. et al. Development of an Artificial Intelligence Model to Guide the Management of Blood Pressure, Fluid Volume, and Dialysis Dose in End-Stage Kidney Disease Patients: Proof of Concept and First Clinical Assessment. Kidney Dis (Basel). 2019;5:28-33

72. Hueso M, Navarro E, Sandoval D, Cruzado JM. Progress in the Development and Challenges for the Use of Artificial Kidneys and Wearable Dialysis Devices. Kidney Dis (Basel). 2019;5:3-10

73. Gura V, Rivara MB, Bieber S, Munshi R, Smith NC, Linke L. et al. A wearable artificial kidney for patients with end-stage renal disease. JCI insight. 2016 1

74. Kim S, Fissell WH, Humes DH, Roy S. Current strategies and challenges in engineering a bioartificial kidney. Front Biosci (Elite Ed). 2015;7:215-28

75. Kensinger C, Karp S, Kant R, Chui BW, Goldman K, Yeager T. et al. First Implantation of Silicon Nanopore Membrane Hemofilters. ASAIO J. 2016;62:491-5

76. Meng F, Seredych M, Chen C, Gura V, Mikhalovsky S, Sandeman S. et al. MXene Sorbents for Removal of Urea from Dialysate: A Step toward the Wearable Artificial Kidney. ACS nano. 2018;12:10518-28

77. Chen A, Nikitczuk K, Nikitczuk J, Maguire T, Yarmush M. Portable robot for autonomous venipuncture using 3D near infrared image guidance. Technology. 2013;1:72-87

78. Ben-David E, Shochat M, Roth I, Nissenbaum I, Sosna J, Goldberg SN. Evaluation of a CT-Guided Robotic System for Precise Percutaneous Needle Insertion. J Vasc Interv Radiol. 2018;29:1440-6

79. Zhang D, Li Z, Chen K, Xiong J, Zhang X, Wang L. An optical tracker based robot registration and servoing method for ultrasound guided percutaneous renal access. Biomed Eng Online. 2013;12:47

80. Rodriguez M, Salmeron MD, Martin-Malo A, Barbieri C, Mari F, Molina RI. et al. A New Data Analysis System to Quantify Associations between Biochemical Parameters of Chronic Kidney Disease-Mineral Bone Disease. PloS one. 2016;11:e0146801

81. Kleiman RS, LaRose ER, Badger JC, Page D, Caldwell MD, Clay JA. et al. Using Machine Learning Algorithms to Predict Risk for Development of Calciphylaxis in Patients with Chronic Kidney Disease. AMIA Jt Summits Transl Sci Proc. 2018;2017:139-46

82. Liu Y, Zhang Y, Liu D, Tan X, Tang X, Zhang F. et al. Prediction of ESRD in IgA Nephropathy Patients from an Asian Cohort: A Random Forest Model. Kidney Blood Press Res. 2018;43:1852-64

83. Chen T, Li X, Li Y, Xia E, Qin Y, Liang S. et al. Prediction and Risk Stratification of Kidney Outcomes in IgA Nephropathy. Am J Kidney Dis. 2019;74:300-9

84. Leung RK, Wang Y, Ma RC, Luk AO, Lam V, Ng M. et al. Using a multi-staged strategy based on machine learning and mathematical modeling to predict genotype-phenotype risk patterns in diabetic kidney disease: a prospective case-control cohort analysis. BMC Nephrol. 2013;14:162

85. Dagliati A, Marini S, Sacchi L, Cogni G, Teliti M, Tibollo V. et al. Machine Learning Methods to Predict Diabetes Complications. J Diabetes Sci Technol. 2018;12:295-302

86. Ravizza S, Huschto T, Adamov A, Böhm L, Büsser A, Flöther FF. et al. Predicting the early risk of chronic kidney disease in patients with diabetes using real-world data. Nat Med. 2019;25:57-9

87. Song X, Waitman LR, Hu Y, Yu ASL, Robins D, Liu M. Robust clinical marker identification for diabetic kidney disease with ensemble feature selection. J Am Med Inform Assoc. 2019;26:242-53

88. Makino M, Yoshimoto R, Ono M, Itoko T, Katsuki T, Koseki A. et al. Artificial intelligence predicts the progression of diabetic kidney disease using big data machine learning. Sci Rep. 2019;9:11862

89. Lofaro D, Maestripieri S, Greco R, Papalia T, Mancuso D, Conforti D. et al. Prediction of chronic allograft nephropathy using classification trees. Transplant Proc. 2010;42:1130-3

90. Tang H, Poynton MR, Hurdle JF, Baird BC, Koford JK, Goldfarb-Rumyantzev AS. Predicting three-year kidney graft survival in recipients with systemic lupus erythematosus. ASAIO J. 2011;57:300-9

91. Abdeltawab H, Shehata M, Shalaby A, Khalifa F, Mahmoud A, El-Ghar MA. et al. A Novel CNN-Based CAD System for Early Assessment of Transplanted Kidney Dysfunction. Sci Rep. 2019;9:5948

92. Coca SG, Singanamala S, Parikh CR. Chronic kidney disease after acute kidney injury: a systematic review and meta-analysis. Kidney Int. 2012;81:442-8

93. Sawhney S, Marks A, Fluck N, Levin A, McLernon D, Prescott G. et al. Post-discharge kidney function is associated with subsequent ten-year renal progression risk among survivors of acute kidney injury. Kidney Int. 2017;92:440-52

94. Ishani A, Nelson D, Clothier B, Schult T, Nugent S, Greer N. et al. The magnitude of acute serum creatinine increase after cardiac surgery and the risk of chronic kidney disease, progression of kidney disease, and death. Arch Intern Med. 2011;171:226-33

95. Goldstein SL, Jaber BL, Faubel S, Chawla LS. AKI transition of care: a potential opportunity to detect and prevent CKD. Clin J Am Soc Nephrol. 2013;8:476-83

96. James M, Bouchard J, Ho J, Klarenbach S, LaFrance JP, Rigatto C. et al. Canadian Society of Nephrology commentary on the 2012 KDIGO clinical practice guideline for acute kidney injury. Am J Kidney Dis. 2013;61:673-85

97. James MT, Pannu N, Hemmelgarn BR, Austin PC, Tan Z, McArthur E. et al. Derivation and External Validation of Prediction Models for Advanced Chronic Kidney Disease Following Acute Kidney Injury. JAMA. 2017;318:1787-97

98. Norouzi J, Yadollahpour A, Mirbagheri SA, Mazdeh MM, Hosseini SA. Predicting Renal Failure Progression in Chronic Kidney Disease Using Integrated Intelligent Fuzzy Expert System. Comput Math Methods Med. 2016;2016:6080814

99. Xiao J, Ding R, Xu X, Guan H, Feng X, Sun T. et al. Comparison and development of machine learning tools in the prediction of chronic kidney disease progression. J Transl Med. 2019;17:119

100. Zacharias HU, Altenbuchinger M, Schultheiss UT, Samol C, Kotsis F, Poguntke I. et al. A Novel Metabolic Signature To Predict the Requirement of Dialysis or Renal Transplantation in Patients with Chronic Kidney Disease. J Proteome Res. 2019;18:1796-805

101. Akbilgic O, Obi Y, Potukuchi PK, Karabayir I, Nguyen DV, Soohoo M. et al. Machine Learning to Identify Dialysis Patients at High Death Risk. Kidney Int Rep. 2019;4:1219-29

102. Mezzatesta S, Torino C, Meo P, Fiumara G, Vilasi A. A machine learning-based approach for predicting the outbreak of cardiovascular diseases in patients on dialysis. Comput Methods Programs Biomed. 2019;177:9-15

103. Checcucci E, Autorino R, Cacciamani GE, Amparore D, De Cillis S, Piana A. et al. Artificial intelligence and neural networks in urology: current clinical applications. Minerva Urol Nefrol. 2020;72:49-57

Author contact

Corresponding author: Xiangcheng Xiao (E-mail: xiaoxcedu.cn).

Received 2019-11-13
Accepted 2020-3-17
Published 2020-4-6

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