Abaach M, Morilla I. Learning models for colorectal cancer signature reconstruction and classification in patients with chronic inflammatory bowel disease. Artif Intell Cancer 2022; 3(2): 27-41 [DOI: 10.35713/aic.v3.i2.27]
Corresponding Author of This Article
Ian Morilla, PhD, Assistant Professor, Research Associate, Laboratoire Analyse, Géométrie et Applications, Centre National de la Recherche Scientifique (Unité mixte de Recherche), Université Sorbonne Paris Nord, 99 avenue Jean Baptiste clément, Villetaneuse, Paris 93430, France. morilla@math.univ-paris13.fr
Research Domain of This Article
Mathematical & Computational Biology
Article-Type of This Article
Basic Study
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Table 1 Possible comparisons to be made during the unsupervised (i.e., we do not rely on the type of disease) global analysis of patients following the considered three different strategies
Strategy
Comparison
Strategy 1 (classic)
1 vs (2,3,4)
2 vs (3,4)
3 vs 4
Strategy 2 (1&1)
1 vs 2; 1 vs 3; 1 vs 4
2 vs 1; 2 vs 3; 2 vs 4
3 vs 1; 3 vs 2; 3 vs 4
4 vs 1; 4 vs 2; 4 vs 3
Strategy 3 (pairwise)
1 vs (2,3,4)
2 vs (1,3,4)
3 vs (1,2,4)
4 vs (1,2,3)
Table 2 Summary of patients’ classification predicted by random forests/support vector machines respectively. From left to right: Group of patients, amount of selected miRNA, percentage of success in true positive classification, sensitivity, specificity and their area under the curve
Methods
Nº miRNA
% True classification (95%CI)
Sensitivity
Specificity
AUC
All miRNA
Strategy 1
56
69 (62-75)/69 (62-75)
0.25/0.43
0.93/0.83
0.76/0.74
CD
9
87 (78-93)/86 (77-92)
0.70/0.73
0.96/0.93
0.89/0.92
UC
30
72% (63-80)/76 (67-83)
0.45/0.55
0.86/0.87
0.77/0.81
miRNAs selected by sPLS-DA
Strategy 1
11
69 (62-75)/68 (62-75)
0.36/0.36
0.87/0.86
0.72/0.74
CD
5
80 (70-88)/82 (67-86)
0.67/0.60
0.87/0.87
0.84/0.86
UC
8
73 (64-80)/81 (73-88)
0.48/0.57
0.86/0.93
0.73/0.81
Table 3 All patients contingence matrix of the 56-selected miRNAs by means of random forests and support vector machines methods
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
18
54
31
41
Controls
10
124
23
111
Table 4 Contingence matrix of the 9-selected miRNA and random forests methods for Crohn’s disease patients
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
21
9
22
4
Controls
2
53
8
51
Table 5 Contingence matrix of the 30-selected miRNA and random forests methods for Ulcerative colitis patients
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
19
23
23
19
Controls
11
68
10
69
Table 6 Contingence matrix of the 11-selected miRNA and random forests methods for all patients
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
27
45
26
46
Controls
18
116
19
115
Table 7 Contingence matrix of the 5-selected miRNA and random forests methods for Crohn’s disease patients
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
20
10
20
10
Controls
7
48
5
50
Table 8 Contingence matrix of the 9-selected miRNA and random forests methods for Ulcerative colitis patients.
Predicted by RF Predicted by SVM
Cases
Controls
Cases
Controls
True
Case
20
22
24
18
Controls
11
68
5
74
Citation: Abaach M, Morilla I. Learning models for colorectal cancer signature reconstruction and classification in patients with chronic inflammatory bowel disease. Artif Intell Cancer 2022; 3(2): 27-41