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Serena Guo

Publications and source records attributed to Serena Guo.

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Privacy-preserving causal mediation analysis using distributed electronic health record networks

Electronic health record (EHR) networks provide unprecedented opportunities to study treatment mechanisms at scale, but mediation analyses across institutions are often hindered by privacy and governance constraints that restrict sharing of patient-level data. We developed a privacy-preserving federated mediation framework that enables estimation of natural direct and indirect effects without exchanging individual-level records across participating sites. The proposed approach integrates renewable learning with counterfactual causal mediation analysis, allowing institutions to collaboratively investigate treatment mechanisms using only low-dimensional summary statistics. Both simulation studies and the real-world application demonstrated that the federated estimator closely reproduced pooled-data results while preserving patient privacy. We applied the method to 32,146 patients in the Indiana Network for Patient Care to evaluate the extent to which body mass index (BMI) mediates the effect of GLP-1 receptor agonist on glycated hemoglobin (HbA1c) reduction. The BMI-mediated pathway accounted for only a small proportion of the overall treatment effect, suggesting that most glycemic improvement occurred through mechanisms other than weight loss.

stat.AP

Feasibility of Identifying Factors Related to Alzheimer's Disease and Related Dementia in Real-World Data

A comprehensive view of factors associated with AD/ADRD will significantly aid in studies to develop new treatments for AD/ADRD and identify high-risk populations and patients for prevention efforts. In our study, we summarized the risk factors for AD/ADRD by reviewing existing meta-analyses and review articles on risk and preventive factors for AD/ADRD. In total, we extracted 477 risk factors in 10 categories from 537 studies. We constructed an interactive knowledge map to disseminate our study results. Most of the risk factors are accessible from structured Electronic Health Records (EHRs), and clinical narratives show promise as information sources. However, evaluating genomic risk factors using RWD remains a challenge, as genetic testing for AD/ADRD is still not a common practice and is poorly documented in both structured and unstructured EHRs. Considering the constantly evolving research on AD/ADRD risk factors, literature mining via NLP methods offers a solution to automatically update our knowledge map.

cs.AI