Prediction of dyslipidemia using gene mutations, family history of diseases and anthropometric indicators in children and adolescents: The CASPIAN-III study

被引:16
作者
Marateb, Hamid R. [1 ,2 ]
Mohebian, Mohammad Reza [1 ]
Javanmard, Shaghayegh Haghjooy [3 ]
Tavallaei, Amir Ali [1 ]
Tajadini, Mohammad Hasan [4 ]
Heidari-Beni, Motahar [5 ]
Angel Mananas, Miguel [2 ,6 ]
Motlagh, Mohammad Esmaeil [7 ]
Heshmat, Ramin [8 ]
Mansourian, Marjan [3 ,9 ]
Kelishadi, Roya [10 ]
机构
[1] Univ Isfahan, Fac Engn, Dept Biomed Engn, Esfahan, Iran
[2] UPC, BarcelonaTech, Dept Automat Control, Biomed Engn Res Ctr, Barcelona, Spain
[3] Isfahan Univ Med Sci, Isfahan Cardiovasc Res Inst, Appl Physiol Res Ctr, Esfahan, Iran
[4] Tarbiat Modares Univ, Dept Clin Biochem, Tehran, Iran
[5] Isfahan Univ Med Sci, Res Inst Primordial Prevent Noncommunicable Dis, Child Growth & Dev Res Ctr, Nutr Dept, Esfahan, Iran
[6] Biomat & Nanomed CIBER BBN, Biomed Res Networking Ctr Bioengn, Barcelona, Spain
[7] Ahvaz Jundishapur Univ Med Sci, Dept Pediat, Ahvaz, Iran
[8] Univ Tehran Med Sci, Endocrinol & Metab Populat Sci Inst, Chron Dis Res Ctr, Dept Epidemiol, Tehran, Iran
[9] Isfahan Univ Med Sci, Fac Hlth, Biostat & Epidemiol Dept, Esfahan, Iran
[10] Isfahan Univ Med Sci, Res Inst Primordial Prevent Noncommunicable Dis, Child Growth & Dev Res Ctr, Pediat Dept, Esfahan, Iran
来源
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL | 2018年 / 16卷
关键词
Computer-assisted diagnosis; Deep learning; Dyslipidemia; Genomics; Health promotion; Machine learning; COMPUTER-AIDED-DIAGNOSIS; ISCHEMIC-HEART-DISEASE; BODY-MASS INDEX; LIPOPROTEIN-LIPASE; CARDIOVASCULAR-DISEASE; LIPID-LEVELS; MIDDLE-EAST; PEDIATRIC POPULATION; PRIMARY PREVENTION; BIRTH-WEIGHT;
D O I
10.1016/j.csbj.2018.02.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dyslipidemia, the disorder of lipoprotein metabolism resulting in high lipid profile, is an important modifiable risk factor for coronary heart diseases. It is associated with more than four million worldwide deaths per year. Half of the children with dyslipidemia have hyperlipidemia during adulthood, and its prediction and screening are thus critical. We designed a new dyslipidemia diagnosis system. The sample size of 725 subjects (age 14.66 +/- 2.61 years; 48% male; dyslipidemia prevalence of 42%) was selected by multistage random cluster sampling in Iran. Single nucleotide polymorphisms (rs1801177, rs708272, rs320, rs328, rs2066718, rs2230808, rs5880, rs5128, rs2893157, rs662799, and Apolipoprotein-E2/E3/E4), and anthropometric, life-style attributes, and family history of diseases were analyzed. A framework for classifying mixed-type data in imbalanced datasetswas proposed. It included internal featuremapping and selection, re-sampling, optimized group method of data handling using convex and stochastic optimizations, a new cost function for imbalanced data and an internal validation. Its performance was assessed using hold-out and 4-fold-cross-validation. Four other classifiers namely as supported vector machines, decision tree, and multilayer perceptron neural network and multiple logistic regression were also used. The average sensitivity, specificity, precision and accuracy of the proposed system were 93%, 94%, 94% and 92%, respectively in cross validation. It significantly outperformed the other classifiers and also showed excellent agreement and high correlation with the gold standard. A non-invasive economical version of the algorithm was also implemented suitable for low-and middle-income countries. It is thus a promising new tool for the prediction of dyslipidemia. (c) 2018 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:121 / 130
页数:10
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