Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 5 min ago
Peer-reviewedCC BYEndocrinology, diabetes & metabolism

Body Composition Phenotypes and Their Metabolic Associations in Treatment-Naïve Patients With Newly Diagnosed Type 2 Diabetes: A DXA-Based Cluster Analysis.

  1. 1Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
  2. 2Department of Endocrinology, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.

Abstract

Background and aims

We characterized body-composition heterogeneity in treatment-naive type 2 diabetes (T2DM) using dual-energy X-ray absorptiometry (DXA), and assessed whether cluster-metabolic associations persisted after accounting for sex-related body-composition differences.Methods

K-means clustering of 50 DXA-derived body-composition variables classified 185 treatment-naive T2DM patients. Variance decomposition, sex-stratified analyses, sex-stratified clustering, sex-specific standardization clustering and multiple imputation (20 datasets) addressed sex confounding and missing data.Results

Four exploratory body-composition clusters were identified: Low Fat-Low Muscle, Male-Predominant Central Obesity (98.6% male), Female-Predominant Low-Muscle High-Adiposity (98.0% female) and High Fat-High Muscle. Two clusters showed strong sex predominance; sex-specific normalization reduced sex-cluster dependence while preserving metabolic associations. In multiple-imputation-adjusted models, Clusters 2 and 4 had markedly higher MASLD odds (OR = 9.69 and 8.55, respectively), while Cluster 4 had lower osteoporosis (OR = 0.16) and higher hyperuricemia (OR = 6.36) odds versus Cluster 1. Bone turnover markers, diabetic retinopathy and diabetic kidney disease showed no significant associations.Conclusions

DXA-based body-composition clusters are associated with distinct metabolic and comorbidity profiles-particularly MASLD, osteoporosis and hyperuricemia-that persisted after sex-specific standardization and multiple imputation. Given the sex-cluster overlap and modest silhouette width, these findings are hypothesis-generating and require prospective validation.

Related

  1. Physical activity phenotypes identified by latent class analysis and their associations with metabolic syndrome among Korean adults
    Yuntae Ju, Joohyun Lee, Dae-Hee Kim +1
    BMC Public HealthPeer-reviewedCC BY-NC-ND 4.0PhysiologyCrossref
  2. Telomere-Independent Associations of hTERT Promoter Polymorphisms with Metabolic Phenotypes and Diabetic Complications
    Krzysztof Sawicki, Małgorzata Suchecka, Magdalena Matysiak-Kucharek +4
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0Full textPhysiologyCrossrefEurope PMC
  3. Physical activity phenotypes from volume-based versus intensity-based wearable metrics: discordant classification and divergent metabolomic, body composition, and cardiac magnetic resonance associations
    Sarah Shi Sien Goh, Khung Keong Yeo, Khung Keong Yeo +9
    Frontiers in Digital HealthPeer-reviewedCC BYFull textPhysiologyDOAJ
  4. Effectiveness of metformin as initial treatment on the metabolic profile of Saudi patients newly diagnosed with type 2 diabetes mellitus : A prospective observational study
    Huda Alkreathy, Fawaz Abdullah Alharbi, Rania Magadmi +8
    MedicinePeer-reviewedCC BY-NCFull textGeneral medicineEurope PMCPMC
  5. Dysfunctional Sleep Beliefs and Attitudes in Major Depressive Disorder: Dimensional Associations with Clinical Phenotypes and Gut-Neuroimmune-Metabolic-Oxidative Pathways
    M. Wang, M. Niu, X. Luo +7
    medRxivPreprintCC BY-NDFull textPsychiatry & mental healthmedRxiv
BibTeX
@article{zhang2026body,
  title = {{Body Composition Phenotypes and Their Metabolic Associations in Treatment-Naïve Patients With Newly Diagnosed Type 2 Diabetes: A DXA-Based Cluster Analysis.}},
  author = {Xintong Zhang and Rui Zhang and Tao Jiang},
  journal = {Endocrinology, diabetes \& metabolism},
  year = {2026},
  month = oct,
  doi = {10.1002/edm2.70366},
  url = {https://europepmc.org/article/MED/42897745},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Body Composition Phenotypes and Their Metabolic Associations in Treatment-Naïve Patients With Newly Diagnosed Type 2 Diabetes: A DXA-Based Cluster Analysis.
AU  - Xintong Zhang
AU  - Rui Zhang
AU  - Tao Jiang
PY  - 2026
DA  - 2026/10/30
JO  - Endocrinology, diabetes & metabolism
DO  - 10.1002/edm2.70366
UR  - https://europepmc.org/article/MED/42897745
AB  - Background and aims  We characterized body-composition heterogeneity in treatment-naive type 2 diabetes (T2DM) using dual-energy X-ray absorptiometry (DXA), and assessed whether cluster-metabolic associations persisted after accounting for sex-related body-composition differences.Methods  K-means clustering of 50 DXA-derived body-composition variables classified 185 treatment-naive T2DM patients. Variance decomposition, sex-stratified analyses, sex-stratified clustering, sex-specific standardization clustering and multiple imputation (20 datasets) addressed sex confounding and missing data.Results  Four exploratory body-composition clusters were identified: Low Fat-Low Muscle, Male-Predominant Central Obesity (98.6% male), Female-Predominant Low-Muscle High-Adiposity (98.0% female) and High Fat-High Muscle. Two clusters showed strong sex predominance; sex-specific normalization reduced sex-cluster dependence while preserving metabolic associations. In multiple-imputation-adjusted models, Clusters 2 and 4 had markedly higher MASLD odds (OR = 9.69 and 8.55, respectively), while Cluster 4 had lower osteoporosis (OR = 0.16) and higher hyperuricemia (OR = 6.36) odds versus Cluster 1. Bone turnover markers, diabetic retinopathy and diabetic kidney disease showed no significant associations.Conclusions  DXA-based body-composition clusters are associated with distinct metabolic and comorbidity profiles-particularly MASLD, osteoporosis and hyperuricemia-that persisted after sex-specific standardization and multiple imputation. Given the sex-cluster overlap and modest silhouette width, these findings are hypothesis-generating and require prospective validation.
SN  - 2398-9238
ER  -