SynthesisCurrent microbiology2025
Diabetes Mellitus, a Leading Comorbidity in COVID-19: an Insight on Pathophysiology, Molecular Interactions, and Comprehensive Management.
Synthesis in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Transcending risk factors: the implications of redefining diabetes as an immunometabolic disease for infectious disease studies.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Coronavirus disease 2019 (COVID-19) has triggered a global pandemic with widespread disruption. Its mortality rate is notably higher in individuals with coexisting non-communicable diseases, particularly diabetes mellitus (DM). Despite extensive efforts, there remains no definitive treatment for COVID-19, making it imperative to protect populations with pre-existing risk factors that predispose them to severe or fatal outcomes. In this systematic literature review, we delineate the key biological and clinical risk factors-specifically, chronic hyperglycemia, endothelial dysfunction, and dysregulated angiotensin-converting enzyme 2 (ACE2) expression-that may exacerbate COVID-19 severity in diabetic patients. We explore how immune and inflammatory pathways intersect with COVID-19 pathogenesis and contribute to differential clinical manifestations in diabetic versus non-diabetic individuals. Particular emphasis is placed on the pathophysiological mechanisms facilitating viral entry and propagation in diabetic patients. Currently, insulin is the primary therapeutic modality for managing acute hyperglycemia in COVID-19, while sodium-glucose cotransporter 2 (SGLT2) inhibitors are generally discouraged due to potential adverse outcomes. As existing evidence is largely preliminary, further research is essential to establish optimized treatment strategies for this vulnerable patient population.
Indexed as
Identifiers
40668418What Socratic holds
Registered trials
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.