As the volume of electronic medical data grows, understanding disease progression and identifying risk factors have become central to public health research. Disease trajectories provide valuable insights into disease progression and risk factors. LUKB DT (LUKB Disease Trajectories) is a user-friendly web tool designed to facilitate disease trajectory analysis using electronic medical records (EMR), particularly the UK Biobank data. LUKB DT processes EMR data, including patient ID, disease diagnoses, corresponding timestamps, and other relevant variables, combining Cox regression, binomial tests, and conditional logistic regression to identify disease trajectories. This tool offers a quick and efficient way to prepare and analyze disease trajectories, contributing to the expanding field of disease trajectory research and providing valuable insights for risk factor identification and disease progression studies. Detailed deployment and usage can be found in the Supplementary Material. LUKB DT is freely available at https://github.com/HaiGenBuShang/LUKB.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis work was supported by supported by Shanghai Municipal Science and Technology Major Project (2023SHZDZX02 and 2017SHZDZX01 to L.J.), the National Natural Science Foundation of China (82394432) and has been conducted using the UK Biobank Resource under Application Number 103791.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The study used (or will use) ONLY openly available human data that were originally located at: UK Biobank (https://www.ukbiobank.ac.uk/).
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced are available online at UK Biobank (https://www.ukbiobank.ac.uk/).
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