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Application of the back-error propagation artificial neural network (BPANN) on genetic variants in the PPAR-γ and RXR-α gene and risk of metabolic syndrome in a Chinese Han population

机译:反向误差传播人工神经网络(BPANN)在中国汉族人群PPAR-γ和RXR-α基因遗传变异和代谢综合征风险中的应用

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摘要

This study was aimed to explore the associations between the combined effects of several polymorphisms in the PPAR-γ and RXR-α gene and environmental factors with the risk of metabolic syndrome by back-error propagation artificial neural network (BPANN). We established the model based on data gathered from metabolic syndrome patients (n = 1012) and normal controls (n = 1069) by BPANN. Mean impact value (MIV) for each input variable was calculated and the sequence of factors was sorted according to their absolute MIVs. Generalized multifactor dimensionality reduction (GMDR) confirmed a joint effect of PPAR-γ and RXR-α based on the results from BPANN. By BPANN analysis, the sequences according to the importance of metabolic syndrome risk factors were in the order of body mass index (BMI), serum adiponectin, rs4240711, gender, rs4842194, family history of type 2 diabetes, rs2920502, physical activity, alcohol drinking, rs3856806, family history of hypertension, rs1045570, rs6537944, age, rs17817276, family history of hyperlipidemia, smoking, rs1801282 and rs3132291. However, no polymorphism was statistically significant in multiple logistic regression analysis. After controlling for environmental factors, A1, A2, B1 and B2 (rs4240711, rs4842194, rs2920502 and rs3856806) models were the best models (cross-validation consistency 10/10, P = 0.0107) with the GMDR method. In conclusion, the interaction of the PPAR-γ and RXR-α gene could play a role in susceptibility to metabolic syndrome. A more realistic model is obtained by using BPANN to screen out determinants of diseases of multiple etiologies like metabolic syndrome.
机译:本研究旨在通过反向误差传播人工神经网络(BPANN)探索PPAR-γ和RXR-α基因中的几种多态性与环境因素与代谢综合征风险之间的关联。我们基于BPANN从代谢综合征患者(n = 1012)和正常对照(n = 1069)收集的数据建立了模型。计算每个输入变量的平均影响值(MIV),并根据其绝对MIV排序因子顺序。基于BPANN的结果,广义多维度降维(GMDR)证实了PPAR-γ和RXR-α的联合作用。通过BPANN分析,根据代谢综合征危险因素的重要性排列的顺序为体重指数(BMI),血清脂联素,rs4240711,性别,rs4842194、2型糖尿病家族史,rs2920502,体育活动,饮酒,rs3856806,高血压家族史,rs1045570,rs6537944,年龄,rs17817276,高脂血症家族史,吸烟,rs1801282和rs3132291。但是,在多逻辑回归分析中,没有多态性在统计学上显着。在控制了环境因素之后,使用GMDR方法,A1,A2,B1和B2(rs4240711,rs4842194,rs2920502和rs3856806)模型是最佳模型(交叉验证一致性10/10,P = 0.0107)。总之,PPAR-γ和RXR-α基因的相互作用可能在代谢综合征易感性中起作用。通过使用BPANN筛选多种病因(如代谢综合征)的疾病的决定因素,可以获得更现实的模型。

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