Trial reportClinical and translational science2025
Development of a Novel Machine Learning Method for Estimation of Life-Long Chronic Disease Progression and Its Application to Type 2 Diabetes.
Trial report in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT00000620. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Action to Control Cardiovascular Risk in Diabetes (ACCORD)
Who cites it
1 citing paper in PubMed.
- Development of a Novel Machine Learning Method for Estimation of Life-Long Chronic Disease Progression and Its Application to Type 2 Diabetes.Clinical and translational science · 2025Trial
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Individual predictions of long-term chronic disease progression from data of limited duration provide valuable insights into estimating patient outcomes and therapeutic needs. Statistical Restoration of Fragmented Time course (SReFT) was developed to address this challenge, yet it is computationally too intensive for large-scale datasets. Although diabetes is a representative chronic disease with significant medical needs, it has been challenging to analyze long-term changes using large-scale patient data due to this limitation. In this study, we aimed to develop a new method (SReFT-machine learning, SReFT-ML) by applying machine learning to the concept of SReFT, and to confirm its performance using synthetic data and the data from a clinical trial, the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial (N = 10,251). SReFT-ML has successfully analyzed both synthetic and clinical data, and reconstructed biomarker trajectories over a 30-year period in patients with diabetes. Decreases in diastolic blood pressure and renal function may be important indicators of disease progression. Furthermore, although age and mortality data were not included in the model, survival analysis demonstrated a clear trend of hazard increases in mortality and diabetes-related outcomes with disease progression. This study introduced machine learning to enhance long-term disease progression modeling. The resulting model characterized a 30-year trajectory of disease risk in diabetes. The results provide a clinically meaningful hypothesis that incorporating systemic factors such as renal function and blood pressure, in addition to classic glycemic control, may enhance comprehensive diabetes care. Trial Registration: ClinicalTrials.gov number: NCT00000620.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.