ReviewHormones (Athens, Greece)2026
Diabetes mellitus as a multisystem disease: understanding subtypes, complications, and the link with steatotic liver diseases in humans.
Review in Hormones (Athens, Greece), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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.
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Who cites it
8 citing papers in PubMed.
- Global trends in the prevalence of type 2 diabetes mellitus: understanding trajectories through conceptual frameworks.Hormones (Athens, Greece) · 2026Review
- Divergent Trajectories of the Burden of MASLD Attributable to High Fasting Plasma Glucose in China and Globally: A GBD Study 1990-2021 and Projections to 2046.Gastroenterology research and practice · 2026Article
- Metabolic heterogeneity at the onset of type 2 diabetes: phenotypes of insulin resistance and β-cell function in the Kazakh population.Frontiers in endocrinology · 2026Article
- Metabolic reprogramming in diabetes and cancer: the role of PI3K/AKT/mTOR and beyond.American journal of cancer research · 2026Review
- Current perspectives on lipid management in diabetic kidney disease: Can fibrates offer advantages over statins for renal outcomes?Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2026Review
- Sarcopenia in the Aging Process: Pathophysiological Mechanisms, Clinical Implications, and Emerging Therapeutic Approaches.International journal of molecular sciences · 2025Review
- Nutrigenomics meets multi-omics: integrating genetic, metabolic, and microbiome data for personalized nutrition strategies.Genes & nutrition · 2025Review
- Unlocking the heterogeneity of pediatric obesity: a phenotypic subtype-based paradigm for precision management.Frontiers in endocrinology · 2025Review
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND & SCOPE OF REVIEW: Diabetes mellitus encompasses a spectrum of metabolic disorders characterized by hyperglycemia. The currently most replicated phenotypic clustering approach, introduced by Ahlqvist et al. and validated by Zaharia et al., identified subtypes based on clinical presentation and underlying pathophysiology. This classification aims at predicting complication risk and enabling targeted therapies. Our review explores shared and distinct mechanisms driving complications, focusing on cardiovascular disease and metabolic dysfunction-associated steatotic liver disease (MASLD), both strongly linked to insulin resistance. We also summarize treatment strategies targeting both conditions and outline mechanisms specific to the development of diabetic foot syndrome, exemplifying the continuum from localized to systemic complications.
methodsWe conducted a narrative review of human and translational studies, focusing on mechanisms and treatments across the above phenotype-based diabetes subtypes, given their reproducibility across populations. MAIN
resultsDiabetes is a multisystem disorder involving a cascade of metabolic disturbances. These include mitochondrial adaptations in key metabolically active tissues contributing to systemic and tissue-specific insulin resistance. Inflammation, inadequate immune responses, oxidative stress, and genetic and environmental factors shape the development of comorbidities whose prevalence varies across subtypes. The interplay between MASLD and diabetes forms a vicious cycle of metabolic abnormalities. Novel treatments show promise in both liver and glycemic endpoints.
conclusionPhenotype-based diabetes subtypes exhibit distinct underlying pathophysiological mechanisms which shape the development of complications, with insulin resistance serving as the central link. Targeting these pathways can pave the way for personalized diabetes therapies.
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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.