TY - JOUR
T1 - Data-driven phenotypic profiling of prediabetes reveals heterogeneous cardiometabolic risks in Chinese adults
AU - 4C study author
AU - Jia, Xiaojing
AU - Wang, Shuangyuan
AU - Wang, Jinfeng
AU - Ding, Yilan
AU - Li, Mian
AU - Lin, Yiting
AU - Zheng, Ruizhi
AU - Huang, Feiyue
AU - Wei, Huapeng
AU - Hu, Chunyan
AU - Xu, Yu
AU - Lin, Hong
AU - Xu, Min
AU - Wang, Tiange
AU - Qiao, Hong
AU - Qin, Guijun
AU - Qin, Yingfen
AU - Tang, Xulei
AU - Ye, Zhen
AU - Hu, Ruying
AU - Shi, Lixin
AU - Su, Qing
AU - Yu, Xuefeng
AU - Yan, Li
AU - Wan, Qin
AU - Chen, Gang
AU - Gao, Zhengnan
AU - Wang, Guixia
AU - Shen, Feixia
AU - Gu, Xuejiang
AU - Luo, Zuojie
AU - Chen, Li
AU - Hou, Xinguo
AU - Li, Qiang
AU - Huo, Yanan
AU - Zhang, Yinfei
AU - Zeng, Tianshu
AU - Liu, Chao
AU - Wang, Youmin
AU - Wu, Shengli
AU - Yang, Tao
AU - Deng, Huacong
AU - Li, Donghui
AU - Lai, Shenghan
AU - Chen, Lulu
AU - Zhao, Jiajun
AU - Mu, Yiming
AU - Ning, Guang
AU - Bi, Yufang
AU - Wang, Weiqing
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2026/12
Y1 - 2026/12
N2 - Background: The heterogeneous and complex nature of prediabetes presents a major challenge in identifying individuals predisposed to developing incident diabetes and related complications. We aimed to identify phenotypic subgroups of prediabetes at risk and to explore their distinct associations with cardiometabolic outcomes. Methods: This study included 79,000 individuals with prediabetes from the three large-scale prospective cohorts in China. Phenotypic heterogeneity was identified using a soft-clustering algorithm based on the proximity network derived from uniform manifold approximation and projection (UMAP), combined with graph-clustering and Gaussian mixture models. Associations between phenotype probabilities and the incidence of type 2 diabetes (T2D), cardiovascular disease (CVD), and kidney events were assessed to evaluate risk differences across the identified profiles. Results: Six phenotypic profiles were identified, including five with distinct metabolic features (representing ~ 70% of the total population), and one without significant features. These profiles demonstrated substantial differences in both baseline cardiometabolic burden and future disease risk. For instance, individuals with a 20% higher probability of belonging to the hypertensive profile had a 9, 6, and 12% higher risk of T2D, CVD, and CKD, respectively, while the profile with high lipids, creatinine, and liver enzyme was associated with an 10% increased risk of T2D and kidney events. Moreover, incorporating phenotypic probabilities into multivariable models significantly improved the prediction of disease risks (likelihood ratio test, P < 0.05). Conclusions: Prediabetes exhibits substantial phenotypic heterogeneity, and delineation of distinct metabolic profiles enables refined risk stratification and informs precision prevention strategies.
AB - Background: The heterogeneous and complex nature of prediabetes presents a major challenge in identifying individuals predisposed to developing incident diabetes and related complications. We aimed to identify phenotypic subgroups of prediabetes at risk and to explore their distinct associations with cardiometabolic outcomes. Methods: This study included 79,000 individuals with prediabetes from the three large-scale prospective cohorts in China. Phenotypic heterogeneity was identified using a soft-clustering algorithm based on the proximity network derived from uniform manifold approximation and projection (UMAP), combined with graph-clustering and Gaussian mixture models. Associations between phenotype probabilities and the incidence of type 2 diabetes (T2D), cardiovascular disease (CVD), and kidney events were assessed to evaluate risk differences across the identified profiles. Results: Six phenotypic profiles were identified, including five with distinct metabolic features (representing ~ 70% of the total population), and one without significant features. These profiles demonstrated substantial differences in both baseline cardiometabolic burden and future disease risk. For instance, individuals with a 20% higher probability of belonging to the hypertensive profile had a 9, 6, and 12% higher risk of T2D, CVD, and CKD, respectively, while the profile with high lipids, creatinine, and liver enzyme was associated with an 10% increased risk of T2D and kidney events. Moreover, incorporating phenotypic probabilities into multivariable models significantly improved the prediction of disease risks (likelihood ratio test, P < 0.05). Conclusions: Prediabetes exhibits substantial phenotypic heterogeneity, and delineation of distinct metabolic profiles enables refined risk stratification and informs precision prevention strategies.
KW - Cardiovascular disease
KW - Clustering
KW - Diabetes
KW - Heterogeneity
KW - Kidney events
KW - Prediabetes
UR - https://www.scopus.com/pages/publications/105026910262
UR - https://www.scopus.com/pages/publications/105026910262#tab=citedBy
U2 - 10.1186/s12933-025-03008-9
DO - 10.1186/s12933-025-03008-9
M3 - Article
C2 - 41331573
AN - SCOPUS:105026910262
SN - 1475-2840
VL - 25
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 3
ER -