Meng Wang

h-index8
2papers
184citations

2 Papers

6.2CVJul 7, 2025Code
Parameterized Diffusion Optimization enabled Autoregressive Ordinal Regression for Diabetic Retinopathy Grading

Qinkai Yu, Wei Zhou, Hantao Liu et al.

As a long-term complication of diabetes, diabetic retinopathy (DR) progresses slowly, potentially taking years to threaten vision. An accurate and robust evaluation of its severity is vital to ensure prompt management and care. Ordinal regression leverages the underlying inherent order between categories to achieve superior performance beyond traditional classification. However, there exist challenges leading to lower DR classification performance: 1) The uneven distribution of DR severity levels, characterized by a long-tailed pattern, adds complexity to the grading process. 2)The ambiguity in defining category boundaries introduces additional challenges, making the classification process more complex and prone to inconsistencies. This work proposes a novel autoregressive ordinal regression method called AOR-DR to address the above challenges by leveraging the clinical knowledge of inherent ordinal information in DR grading dataset settings. Specifically, we decompose the DR grading task into a series of ordered steps by fusing the prediction of the previous steps with extracted image features as conditions for the current prediction step. Additionally, we exploit the diffusion process to facilitate conditional probability modeling, enabling the direct use of continuous global image features for autoregression without relearning contextual information from patch-level features. This ensures the effectiveness of the autoregressive process and leverages the capabilities of pre-trained large-scale foundation models. Extensive experiments were conducted on four large-scale publicly available color fundus datasets, demonstrating our model's effectiveness and superior performance over six recent state-of-the-art ordinal regression methods. The implementation code is available at https://github.com/Qinkaiyu/AOR-DR.

8.4AIDec 24, 2017
Predicting Rich Drug-Drug Interactions via Biomedical Knowledge Graphs and Text Jointly Embedding

Meng Wang

Minimizing adverse reactions caused by drug-drug interactions has always been a momentous research topic in clinical pharmacology. Detecting all possible interactions through clinical studies before a drug is released to the market is a demanding task. The power of big data is opening up new approaches to discover various drug-drug interactions. However, these discoveries contain a huge amount of noise and provide knowledge bases far from complete and trustworthy ones to be utilized. Most existing studies focus on predicting binary drug-drug interactions between drug pairs but ignore other interactions. In this paper, we propose a novel framework, called PRD, to predict drug-drug interactions. The framework uses the graph embedding that can overcome data incompleteness and sparsity issues to achieve multiple DDI label prediction. First, a large-scale drug knowledge graph is generated from different sources. Then, the knowledge graph is embedded with comprehensive biomedical text into a common low dimensional space. Finally, the learned embeddings are used to efficiently compute rich DDI information through a link prediction process. To validate the effectiveness of the proposed framework, extensive experiments were conducted on real-world datasets. The results demonstrate that our model outperforms several state-of-the-art baseline methods in terms of capability and accuracy.