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Ning Meng

Publications and source records attributed to Ning Meng.

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Identifying Unique Spatial-Temporal Bayesian Network without Markov Equivalence

Identifying vanilla Bayesian network to model spatial-temporal causality can be a critical yet challenging task. Different Markovian-equivalent directed acyclic graphs would be identified if the identifiability is not satisfied. To address this issue, Directed Cyclic Graph is proposed to drop the directed acyclic constraint. But it does not always hold, and cannot model dynamical time-series process. Then, Full Time Graph is proposed with introducing high-order time delay. Full Time Graph has no Markov equivalence class by assuming no instantaneous effects. But, it also assumes that the causality is invariant with varying time, that is not always satisfied in the spatio-temporal scenarios. Thus, in this work, a Spatial-Temporal Bayesian Network (STBN) is proposed to theoretically model the spatial-temporal causality from the perspective of information transfer. STBN explains the disappearance of network structure $X\rightarrow Z \rightarrow Y$ and $X\leftarrow Z \leftarrow Y$ by the principle of information path blocking. And finally, the uniqueness of STBN is proved. Based on this, a High-order Causal Entropy (HCE) algorithm is also proposed to uniquely identify STBN under time complexity $\mathcal{O}(n^3\tau_{max})$, where $n$ is the number of variables and $\tau_{max}$ is the maximum time delay. Numerical experiments are conducted with comparison to other baseline algorithms. The results show that HCE algorithm obtains state-of-the-art identification accuracy. The code is available at https://github.com/KMY-SEU/HCE.

cs.AI

Prediction of Coronary Heart Disease Using Routine Blood Tests

Background --The objective of this study was to examine the association of routine blood test results with coronary heart disease (CHD) risk, to incorporate them into coronary prediction models and to compare the discrimination properties of this approach with other prediction functions. Methods and Results --This work was designed as a retrospective, single-center study of a hospital-based cohort. The 5060 CHD patients (2365 men and 2695 women) were 1 to 97 years old at baseline with 8 years (2009-2017) of medical records, 5051 health check-ups and 5075 cases of other diseases. We developed a two-layer Gradient Boosting Decision Tree(GBDT) model based on routine blood data to predict the risk of coronary heart disease, which could identify 86% of people with coronary heart disease. We built a dataset with 15,000 routine blood tests results. Using this dataset, we trained the two-layer GBDT model to classify healthy status, coronary heart disease and other diseases. As a result of the classification after machine learning, we found that the sensitivity of detecting the health data was approximately 93% for all data, and the sensitivity of detecting CHD was 93% for disease data that included coronary heart disease. On this basis, we further visualized the correlation between routine blood results and related data items, and there was an obvious pattern in health and coronary heart disease in all data presentations, which can be used for clinical reference. Finally, we briefly analyzed the results above from the perspective of pathophysiology. Conclusions --Routine blood data provides more information about CHD than what we already know through the correlation between test results and related data items. A simple coronary disease prediction model was developed using a GBDT algorithm, which will allow physicians to predict CHD risk in patients without overt CHD.

physics.med-ph