A deep learning approach to predict blood-brain barrier permeability

被引:11
作者
Alsenan, Shrooq [1 ]
Al-Turaiki, Isra [2 ]
Hafez, Alaaeldin [3 ]
机构
[1] Princess Nourah bint Abdulrahman Univ, Coll Comp & Informat Sci, Informat Syst Dept, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Comp & Informat Sci, Informat Technol Dept, Riyadh, Saudi Arabia
[3] King Saud Univ, Coll Comp & Informat Sci, Informat Syst Dept, Riyadh, Saudi Arabia
关键词
Chemoinformatics; Convolutional Neural Network (CNN); Blood Brain Barrier (BBB) permeability; Quantitative Structure-Activity Relationships (QSAR); IN-SILICO PREDICTION; FEATURE-SELECTION; NEURAL-NETWORKS; CLASSIFICATION; MODEL; VALIDATION;
D O I
10.7717/peerj-cs.515
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
The blood-brain barrier plays a crucial role in regulating the passage of 98% of the compounds that enter the central nervous system (CNS). Compounds with high permeability must be identified to enable the synthesis of brain medications for the treatment of various brain diseases, such as Parkinson's, Alzheimer's, and brain tumors. Throughout the years, several models have been developed to solve this problem and have achieved acceptable accuracy scores in predicting compounds that penetrate the blood-brain barrier. However, predicting compounds with "low" permeability has been a challenging task. In this study, we present a deep learning (DL) classification model to predict blood-brain barrier permeability. The proposed model addresses the fundamental issues presented in former models: high dimensionality, class imbalances, and low specificity scores. We address these issues to enhance the high-dimensional, imbalanced dataset before developing the classification model: the imbalanced dataset is addressed using oversampling techniques and the high dimensionality using a nonlinear dimensionality reduction technique known as kernel principal component analysis (KPCA). This technique transforms the high-dimensional dataset into a low-dimensional Euclidean space while retaining invaluable information. For the classification task, we developed an enhanced feed-forward deep learning model and a convolutional neural network model. In terms of specificity scores (i.e., predicting compounds with low permeability), the results obtained by the enhanced feed-forward deep learning model outperformed those obtained by other models in the literature that were developed using the same technique. In addition, the proposed convolutional neural network model surpassed models used in other studies in multiple accuracy measures, including overall accuracy and specificity. The proposed approach solves the problem inevitably faced with obtaining low specificity resulting in high false positive rate.
引用
收藏
页码:1 / 26
页数:26
相关论文
共 58 条
[1]  
Al-Turaiki I, 2020, 3 INT C COMPUTER APP, P65
[2]  
Alvascience Srl, 2019, ALVADESC
[3]   A survey of cross-validation procedures for model selection [J].
Arlot, Sylvain ;
Celisse, Alain .
STATISTICS SURVEYS, 2010, 4 :40-79
[4]   In-vitro blood-brain barrier models for drug screening and permeation studies: an overview [J].
Bagchi, Sounak ;
Chhibber, Tanya ;
Lahooti, Behnaz ;
Verma, Angela ;
Borse, Vivek ;
Jayant, Rahul Dev .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2019, 13 :3591-3605
[5]   THE BLOOD-BRAIN-BARRIER [J].
BRADBURY, MWB .
EXPERIMENTAL PHYSIOLOGY, 1993, 78 (04) :453-472
[6]   Towards Better BBB Passage Prediction Using an Extensive and Curated Data Set [J].
Brito-Sanchez, Yoan ;
Marrero-Ponce, Yovani ;
Barigye, Stephen J. ;
Yaber-Goenaga, Ivan ;
Morell Perez, Carlos ;
Huong Le-Thi-Thu ;
Cherkasov, Artem .
MOLECULAR INFORMATICS, 2015, 34 (05) :308-330
[7]   A Method to Predict Blood-Brain Barrier Permeability of Drug-Like Compounds Using Molecular Dynamics Simulations [J].
Carpenter, Timothy S. ;
Kirshner, Daniel A. ;
Lau, Edmond Y. ;
Wong, Sergio E. ;
Nilmeier, Jerome P. ;
Lightstone, Felice C. .
BIOPHYSICAL JOURNAL, 2014, 107 (03) :630-641
[8]   A Simple Method to Predict Blood-Brain Barrier Permeability of Drug-Like Compounds Using Classification Trees [J].
Castillo-Garit, Juan A. ;
Casanola-Martin, Gerardo M. ;
Huong Le-Thi-Thu ;
Hai Pham-The ;
Barigye, Stephen J. .
MEDICINAL CHEMISTRY, 2017, 13 (07) :664-669
[9]   SMOTE: Synthetic minority over-sampling technique [J].
Chawla, Nitesh V. ;
Bowyer, Kevin W. ;
Hall, Lawrence O. ;
Kegelmeyer, W. Philip .
2002, American Association for Artificial Intelligence (16)
[10]   The rise of deep learning in drug discovery [J].
Chen, Hongming ;
Engkvist, Ola ;
Wang, Yinhai ;
Olivecrona, Marcus ;
Blaschke, Thomas .
DRUG DISCOVERY TODAY, 2018, 23 (06) :1241-1250