Review
Copyright ©The Author(s) 2025.
World J Diabetes. Jul 15, 2025; 16(7): 106218
Published online Jul 15, 2025. doi: 10.4239/wjd.v16.i7.106218
Table 1 Representative multi-omics studies across different diabetes subtypes and complications
Dm subtype/focus
Omics approach(s)
Primary objective/key findings
Ref.
T1DM (human cohorts)Genomics (HLA region); metabolomics (LC-MS); epigenomics (RRBS)Investigate autoimmune-driven β-cell destruction and identify early T1DM biomarkers[1-3]
T2DM (human & animal)Transcriptomics (RNA-Seq); proteomics (LC-MS/MS); metabolomics (NMR)Elucidate insulin resistance, islet dysfunction; discover novel therapeutic targets[8,9]
GDM (human studies)Metabolomics (GC-MS); microbiomics (16S rRNA)Uncover pregnancy-specific metabolite and microbiome signatures predictive of GDM[10,12-15]
DKD/DR complicationsProteomics (targeted); metabolomics (untargeted); ML-based integrationCorrelate inflammatory and fibrotic biomarkers with organ damage; early detection in both T1DM and T2DM[17-20]
GI complicationsMulti-omics synergy (transcript + metabolite)Reveal changes in gut motility, microbiome composition, disease progression in T2DM[25,36,42]
Maternal hyperglycemiaMetabolomics (LC-MS); lipidomicsAssess how hyperglycemia in pregnant sows influences neonatal hepatic metabolism[43]
Microbiome in T1DM/ T2DM/GDMMicrobiomics (16S rRNA, shotgun metagenomics); Metabolomics (SCFAs)Examine gut dysbiosis related to insulin resistance, inflammation, and distinct metabolic phenotypes[62-64]