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ABSTRACT: Objective
This study aimed to identify clinically interpretable DKD sub-phenotypes for personalized prognosis and intervention.Methods
We enrolled participants with type 2 diabetes mellitus (T2DM) from three hospitals in China. Clinically interpretable sub-phenotypes were identified using two complementary clustering frameworks: a static model (k-means clustering) capturing the metabolic-renal profile at DKD diagnosis, and a dynamic model (group-based multi-trajectory model, GBMTM) reconstructing longitudinal trajectories preceding diagnosis. Associations between DKD clusters and post-diagnosis DKD progression were estimated using cox regression.Results
A total of 1520 participants were included for the analysis of static clustering, 32.53% were females with a mean
SUBMITTER: Li K
PROVIDER: S-EPMC13643975 | biostudies-literature | 2026 Jul
REPOSITORIES: biostudies-literature