| Literature DB >> 33968664 |
Jun Tan1,2, Feng Qin1, Jiuhong Yuan1,2.
Abstract
In recent years, the advantages of artificial intelligence (AI) in data processing and model analysis have emerged in the medical field, enabled by computer technology developments and the integration of multiple disciplines. The application of AI in the medical field has gradually deepened and broadened. Among them, the development of clinical medicine intelligent decision-making is the fastest. The advantage of clinical medicine intelligent decision-making is to make the diagnosis faster and more accurate on the basis of certain information. Urine detection technologies, such as urine proteomics, urine metabolomics, and urine RNomics, have developed rapidly with the advancements in omics and medical tests. Advances in urine testing have made it possible to obtain a wealth of information from easily accessible urine. However, it has always been a problem to extract effective information from this information and use it. AI technology provides the possibility to process and use the information in urine. AI, combined with urine detection, not only provides new possibilities for precise and individual diagnosis and disease treatment, but also helps promote non-invasive diagnosis and treatment. This article reviews the research and applications of AI combined with urine detection for disease diagnosis and treatment and discusses its existing problems and future development. 2021 Translational Andrology and Urology. All rights reserved.Entities:
Keywords: Artificial intelligence (AI); diagnosis; omics; urine detection
Year: 2021 PMID: 33968664 PMCID: PMC8100834 DOI: 10.21037/tau-20-1405
Source DB: PubMed Journal: Transl Androl Urol ISSN: 2223-4683
Studies using artificial intelligence combined with urine detection
| Study | Application | Sample size | Training features | Algorithms/modes | Accuracy (%) | Sensitivity | Specificity | AUC (%) | |
|---|---|---|---|---|---|---|---|---|---|
| Training set | Test set | ||||||||
| Rossing | Diagnosed HF | 127 HErEF patients; 581 controls | 94 HFrEF patients | 103 potential HFrEF peptide biomarkers | SVM | NA | 93.6 | 92.9 | 0.972 |
| Zhang | Predicted progression from asymptomatic left ventricular dysfunction to symptomatic HF | 57 patients with HF; 38 patients progressed to HF during follow-up; 192 controls | 175 patients with asymptomatic diastolic left ventricular dysfunction | 96 potential HF peptide biomarkers | SVM | NA | NA | NA | 0.7 |
| Von Zur Mühlen | Identified specific biomarkers for DVT and PE | 17 patients with DVT and DVT+PE; 32 controls | 6 patients with DVT and DVT+PE; 41 controls | 62 urinary peptides | SVM | NA | 100 | 83 | 0.90 |
| Zhang | Identified biomarkers for lung cancer diagnosis | 23 lung cancer; 23 healthy controls | 10 lung cancer; 10 healthy controls | 5 urinary biomarkers | RF | NA | NA | NA | 0.8747–0.9853 |
| Nakajima | Distinguished between CRC, benign diseases, and healthy people | 201 CRCs; 31 non-CRCs | 59 samples | N1, N12diacetylspermine and other 6 polyamines | Decision tree | NA | NA | NA | 0.961 |
| Roux-Dalvai | Identified bacterial species causing UTIs quickly | 190 samples including inoculated and non-inoculated urine | NA | 82 peptides | RF and so on | 100 | NA | NA | 0.98 |
| Eisner | Predicted whether a patient needed colonoscopy | 355 patients required colonoscopy; 633 normal controls | Data set spilt into several folds | NA | SVM; RF; LASSO | NA | 64.00 | 65.00 | 0.715 |
| Shao | Predicted BCa | 87 BCa patients; 65 hernia patients | 47 patients | 6 putative markers | Decision tree | 76.60 | 71.88 | 86.67 | NA |
| Kouznetsova | Identified early and late BCa | Metabolites obtained from publication (McDunn | 205 metabolites of early stage BCa; 42 metabolites of late-stage BCa | All metabolites from the sources | ANN; SGD | 72.00 (for early BCa); | NA | NA | NA |
| Caudarella | Predicted the recurrence of calculus in 5 years | 80 outpatients | NA | 6 parameters from urine of patients | ANN | NA | NA | NA | 0.961 |
| Liang | Searched for metabolic markers of liver cancer | 25 early HCC patients and 12 controls | 15 HCC patient and 10 controls | 15 kinds of urine metabolites | SVM and so on | NA | 96.50 | 83.00 | 0.903 |
| Dykstra | Predicted the tolerance and response of CRC patients who underwent adjuvant chemotherapy | 62 patients with CRC | NA | 12 metabolites | LASSO; SVM; RF; decision tree | NA | NA | NA | 0.750 (the highest) |
| Martinez-Vernon | Built a diabetes prediction model | 72 patients with type II diabetes; 43 healthy controls | NA | Volatile organic compounds in urine | RF; SLR; SVM; ANN | NA | NA | NA | 0.825 |
| Sapre | Constructed a BCa prediction model | 30 patients with active cancer (recurrers); 30 non-recurrers 21 benign controls | NA | 6 parameters from urine of patients | ANN | NA | NA | NA | 0.961 |
| Connell | Found microRNAs related to BCa and constructed a prostate cancer prediction model | 358 prostate patients | 177 prostate patients | Urine-derived EV-RNA profiles | LASSO | NA | NA | NA | 0.770 |
| Sanghvi | Developed a model to process whole slide images and predict diagnoses | 1,615 voided and instrumented urine cytology cases | 790 cases | Hyperchromasia, chromatin coarseness, and nuclear membrane irregularity, N/C | Deep learning | NA | 79.50 | 84.50 | 0.910 |
| Muralidaran | Built an artificial neural networks model to identify urothelial cell carcinoma | 59 urothelial cell carcinoma cases; 56 benign cases | NA | Nuclear area, diameter, standard deviation of nuclear area, and so on | ANN | 100 (all the benign and malignant cases) | NA | NA | NA |
| Heckerling | Predicted urinary tract infections | 212 women presented to an ambulatory clinic with urinary complaints | NA | Urinary frequency, foul urine odor, LE on urine dipstick, and bacteria and epithelial cells on urinalysis | ANN | 0.764 | 0.821 | 0.744 | 0.853 (the best) |
HErEF, heart failure with reduced ejection fraction; support vector machines, support vector machine; HF, heart failure; DVT, deep vein thrombosis; PE, pulmonary embolism; random forests, random forest; MS, metabolic syndrome; CRC, colorectal cancer; EV-RNA, extracellular-vesicle RNA; LASSO, least absolute shrinkage and selection operator; UCB, urothelial carcinoma of the bladder; BCa, bladder cancer; artificial neural networks, artificial neural network; SGD, stochastic gradient descent; HCC, hepatocellular carcinoma; SLR, sparse logistic regression; N/C, nuclear-cytoplasmic ratio; LE, leukocyte esterase.
Figure 1The applications of artificial intelligence combined with urine detection.