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DOI 10.1109/tbme.2019.2897285

Медицинская библиотека · IEEE transactions on bio-medical engineering · 2019

Severe Dengue Prognosis Using Human Genome Data and Machine Learning.

Davi Caio, Pastor Andre, Oliveira Thiego, Neto Fernando B de Lima, Braga-Neto Ulisses, Bigham Abigail W, Bamshad Michael, Marques Ernesto T A, Acioli-Santos Bartolomeu

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Dengue has become one of the most important worldwide arthropod-borne diseases. Dengue phenotypes are based on laboratorial and clinical exams, which are known to be inaccurate.

OBJECTIVE

We present a machine learning approach for the prediction of dengue fever severity based solely on human genome data.

METHODS

One hundred and two Brazilian dengue patients and controls were genotyped for 322 innate immunity single nucleotide polymorphisms (SNPs). Our model uses a support vector machine algorithm to find the optimal loci classification subset and then an artificial neural network (ANN) is used to classify patients into dengue fever or severe dengue.

RESULTS

The ANN trained on 13 key immune SNPs selected under dominant or recessive models produced median values of accuracy greater than 86%, and sensitivity and specificity over 98% and 51%, respectively.

CONCLUSION

The proposed classification method, using only genome markers, can be used to identify individuals at high risk for developing the severe dengue phenotype even in uninfected conditions.

SIGNIFICANCE: Our results suggest that the genetic context is a key element in phenotype definition in dengue. The methodology proposed here is extendable to other Mendelian based and genetically influenced diseases.

Для цитирования: Davi Caio, Pastor Andre, Oliveira Thiego, Neto Fernando B de Lima, Braga-Neto Ulisses, Bigham Abigail W, Bamshad Michael, Marques Ernesto T A, Acioli-Santos Bartolomeu. Severe Dengue Prognosis Using Human Genome Data and Machine Learning.. IEEE transactions on bio-medical engineering. 2019. DOI: 10.1109/tbme.2019.2897285.

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