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1.
Int J Bioinform Res Appl ; 11(3): 233-46, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26561019

RESUMO

This paper aims to enlighten the complex etiology beneath obesity by analysing data from a large nutrigenetics study, in which nutritional and genetic factors associated with obesity were recorded for around two thousand individuals. In our previous work, these data have been analysed using artificial neural network methods, which identified optimised subsets of factors to predict one's obesity status. These methods did not reveal though how the selected factors interact with each other in the obtained predictive models. For that reason, parallel Multifactor Dimensionality Reduction (pMDR) was used here to further analyse the pre-selected subsets of nutrigenetic factors. Within pMDR, predictive models using up to eight factors were constructed, further reducing the input dimensionality, while rules describing the interactive effects of the selected factors were derived. In this way, it was possible to identify specific genetic variations and their interactive effects with particular nutritional factors, which are now under further study.


Assuntos
Mineração de Dados/métodos , Redução Dimensional com Múltiplos Fatores/métodos , Nutrigenômica/métodos , Obesidade/genética , Obesidade/metabolismo , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fenômenos Fisiológicos da Nutrição , Polimorfismo de Nucleotídeo Único , Adulto Jovem
2.
BMC Bioinformatics ; 11: 453, 2010 Sep 08.
Artigo em Inglês | MEDLINE | ID: mdl-20825661

RESUMO

BACKGROUND: Obesity is a multifactorial trait, which comprises an independent risk factor for cardiovascular disease (CVD). The aim of the current work is to study the complex etiology beneath obesity and identify genetic variations and/or factors related to nutrition that contribute to its variability. To this end, a set of more than 2300 white subjects who participated in a nutrigenetics study was used. For each subject a total of 63 factors describing genetic variants related to CVD (24 in total), gender, and nutrition (38 in total), e.g. average daily intake in calories and cholesterol, were measured. Each subject was categorized according to body mass index (BMI) as normal (BMI ≤ 25) or overweight (BMI > 25). Two artificial neural network (ANN) based methods were designed and used towards the analysis of the available data. These corresponded to i) a multi-layer feed-forward ANN combined with a parameter decreasing method (PDM-ANN), and ii) a multi-layer feed-forward ANN trained by a hybrid method (GA-ANN) which combines genetic algorithms and the popular back-propagation training algorithm. RESULTS: PDM-ANN and GA-ANN were comparatively assessed in terms of their ability to identify the most important factors among the initial 63 variables describing genetic variations, nutrition and gender, able to classify a subject into one of the BMI related classes: normal and overweight. The methods were designed and evaluated using appropriate training and testing sets provided by 3-fold Cross Validation (3-CV) resampling. Classification accuracy, sensitivity, specificity and area under receiver operating characteristics curve were utilized to evaluate the resulted predictive ANN models. The most parsimonious set of factors was obtained by the GA-ANN method and included gender, six genetic variations and 18 nutrition-related variables. The corresponding predictive model was characterized by a mean accuracy equal of 61.46% in the 3-CV testing sets. CONCLUSIONS: The ANN based methods revealed factors that interactively contribute to obesity trait and provided predictive models with a promising generalization ability. In general, results showed that ANNs and their hybrids can provide useful tools for the study of complex traits in the context of nutrigenetics.


Assuntos
Doenças Cardiovasculares/etiologia , Redes Neurais de Computação , Nutrigenômica/métodos , Obesidade/etiologia , Adulto , Idoso , Índice de Massa Corporal , Ingestão de Energia , Feminino , Variação Genética , Humanos , Masculino , Pessoa de Meia-Idade , Avaliação Nutricional , Obesidade/complicações , Obesidade/genética , Valor Preditivo dos Testes , Curva ROC , Fatores de Risco , População Branca/genética , Adulto Jovem
3.
Artigo em Inglês | MEDLINE | ID: mdl-19163743

RESUMO

Clinical studies indicate that exaggerated postprandial lipemia is linked to the progression of atherosclerosis, leading cause of Cardiovascular Diseases (CVD). CVD is a multi-factorial disease with complex etiology and according to the literature postprandial Triglycerides (TG) can be used as an independent CVD risk factor. Aim of the current study is to construct an Artificial Neural Network (ANN) based system for the identification of the most important gene-gene and/or gene-environmental interactions that contribute to a fast or slow postprandial metabolism of TG in blood and consequently to investigate the causality of postprandial TG response. The design and development of the system is based on a dataset of 213 subjects who underwent a two meals fatty prandial protocol. For each of the subjects a total of 30 input variables corresponding to genetic variations, sex, age and fasting levels of clinical measurements were known. Those variables provide input to the system, which is based on the combined use of Parameter Decreasing Method (PDM) and an ANN. The system was able to identify the ten (10) most informative variables and achieve a mean accuracy equal to 85.21%.


Assuntos
Doenças Cardiovasculares/complicações , Doenças Cardiovasculares/diagnóstico , Hiperlipidemias/diagnóstico , Hiperlipidemias/etiologia , Redes Neurais de Computação , Doenças Cardiovasculares/genética , Meio Ambiente , Jejum , Feminino , Variação Genética , Humanos , Hiperlipidemias/genética , Masculino , Modelos Genéticos , Modelos Estatísticos , Período Pós-Prandial , Reprodutibilidade dos Testes , Fatores de Risco , Fatores de Tempo
4.
Artigo em Inglês | MEDLINE | ID: mdl-18002811

RESUMO

Aim of this paper is to evaluate the diagnostic contribution of various types of texture features in discrimination of hepatic tissue in abdominal non-enhanced Computed Tomography (CT) images. Regions of Interest (ROIs) corresponding to the classes: normal liver, cyst, hemangioma, and hepatocellular carcinoma were drawn by an experienced radiologist. For each ROI, five distinct sets of texture features are extracted using First Order Statistics (FOS), Spatial Gray Level Dependence Matrix (SGLDM), Gray Level Difference Method (GLDM), Laws' Texture Energy Measures (TEM), and Fractal Dimension Measurements (FDM). In order to evaluate the ability of the texture features to discriminate the various types of hepatic tissue, each set of texture features, or its reduced version after genetic algorithm based feature selection, was fed to a feed-forward Neural Network (NN) classifier. For each NN, the area under Receiver Operating Characteristic (ROC) curves (Az) was calculated for all one-vs-all discriminations of hepatic tissue. Additionally, the total Az for the multi-class discrimination task was estimated. The results show that features derived from FOS perform better than other texture features (total Az: 0.802+/-0.083) in the discrimination of hepatic tissue.


Assuntos
Algoritmos , Inteligência Artificial , Interpretação de Imagem Assistida por Computador/métodos , Neoplasias Hepáticas/diagnóstico por imagem , Reconhecimento Automatizado de Padrão/métodos , Tomografia Computadorizada por Raios X/métodos , Humanos , Aumento da Imagem/métodos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
5.
Artif Intell Med ; 41(1): 25-37, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17624744

RESUMO

OBJECTIVES: The aim of the present study is to define an optimally performing computer-aided diagnosis (CAD) architecture for the classification of liver tissue from non-enhanced computed tomography (CT) images into normal liver (C1), hepatic cyst (C2), hemangioma (C3), and hepatocellular carcinoma (C4). To this end, various CAD architectures, based on texture features and ensembles of classifiers (ECs), are comparatively assessed. MATERIALS AND METHODS: Number of regions of interests (ROIs) corresponding to C1-C4 have been defined by experienced radiologists in non-enhanced liver CT images. For each ROI, five distinct sets of texture features were extracted using first order statistics, spatial gray level dependence matrix, gray level difference method, Laws' texture energy measures, and fractal dimension measurements. Two different ECs were constructed and compared. The first one consists of five multilayer perceptron neural networks (NNs), each using as input one of the computed texture feature sets or its reduced version after genetic algorithm-based feature selection. The second EC comprised five different primary classifiers, namely one multilayer perceptron NN, one probabilistic NN, and three k-nearest neighbor classifiers, each fed with the combination of the five texture feature sets or their reduced versions. The final decision of each EC was extracted by using appropriate voting schemes, while bootstrap re-sampling was utilized in order to estimate the generalization ability of the CAD architectures based on the available relatively small-sized data set. RESULTS: The best mean classification accuracy (84.96%) is achieved by the second EC using a fused feature set, and the weighted voting scheme. The fused feature set was obtained after appropriate feature selection applied to specific subsets of the original feature set. CONCLUSIONS: The comparative assessment of the various CAD architectures shows that combining three types of classifiers with a voting scheme, fed with identical feature sets obtained after appropriate feature selection and fusion, may result in an accurate system able to assist differential diagnosis of focal liver lesions from non-enhanced CT images.


Assuntos
Hepatopatias/diagnóstico , Interpretação de Imagem Radiográfica Assistida por Computador/métodos , Tomografia Computadorizada por Raios X , Algoritmos , Diagnóstico Diferencial , Humanos , Computação Matemática , Redes Neurais de Computação , Reprodutibilidade dos Testes
6.
Comput Biol Chem ; 30(6): 416-24, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17097352

RESUMO

The location of the membrane lipid bilayer relative to a transmembrane protein structure is important in protein engineering. Since it is not present on the determined structures, it is essential to automatically define the membrane embedded protein region in order to test mutation effects or to design potential drugs. beta-Barrel transmembrane proteins, present in nature as outer membrane proteins (OMPs), comprise one of the two transmembrane protein fold classes. Lately, the number of their determined structures has increased and this enables the implementation and evaluation of structure-based annotation methods and their more comprehensive study. In this paper, we propose two new algorithms for (i) the geometric modelling of beta-barrels and (ii) the detection of the transmembrane region of a beta-barrel transmembrane protein. The geometric modelling algorithm combines a non-linear least square minimization method and a genetic algorithm in order to find the characteristics (axis, radius) of a shape with axial symmetry which best models a beta-barrel. The transmembrane region is detected by profiling the external residues of the beta-barrel along its axis in terms of hydrophobicity and existence of aromatic and charged residues. TbB-Tool implements these algorithms and is available in . A non-redundant set of 22 OMPs is used in order to evaluate the algorithms implemented and the results are very satisfying. In addition, we quantify the abundance of all amino acids and the average hydrophobicity for external and internal beta-stranded residues along the axis of beta-barrel, thus confirming and extending other researchers' results.


Assuntos
Bicamadas Lipídicas/química , Proteínas de Membrana/química , Modelos Moleculares , Estrutura Secundária de Proteína , Animais , Proteínas da Membrana Bacteriana Externa/química , Biologia Computacional , Bases de Dados de Proteínas , Humanos , Interações Hidrofóbicas e Hidrofílicas , Dobramento de Proteína
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