Evidence mapPaperPMID 41977405Full record

ReviewInternational journal of molecular sciences2026

Connecting the Dots: Neurobiological Interplay Between Type 2 Diabetes and Alzheimer's Disease.

Analía Foncea-Bitrán, Cristián Barros-Osorio, Francisca Arriaza, Catalina Ramírez-López, Lina M Ruiz, Marlen Barreto, Fernando C Ortiz, Francisca Cornejo, Gonzalo I Gómez

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Analía Foncea-BitránCenter for Integrative Biology, Faculty of Science, Universidad Mayor, Santiago 8580745, Chile.
Cristián Barros-OsorioInstitute of Biomedical Sciences, Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago 8581151, Chile.
Francisca ArriazaMechanisms of Myelin Formation and Repair Laboratory, Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago 8350347, Chile.ORCID 0009-0006-2455-1634
Catalina Ramírez-LópezInstitute of Biomedical Sciences, Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago 8581151, Chile.
Lina M RuizInstitute of Biomedical Sciences, Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago 8581151, Chile.ORCID 0000-0002-9363-2730
Marlen BarretoInstitute of Biomedical Sciences, Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago 8581151, Chile.ORCID 0000-0002-6275-3855
Fernando C OrtizMechanisms of Myelin Formation and Repair Laboratory, Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago 8350347, Chile.ORCID 0000-0002-4776-4492
Francisca CornejoCenter for Integrative Biology, Faculty of Science, Universidad Mayor, Santiago 8580745, Chile.ORCID 0000-0001-9280-3430
Gonzalo I GómezInstitute of Biomedical Sciences, Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago 8581151, Chile.ORCID 0000-0001-7761-8675

Funding

Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT) 1250485
6 · The paper itself

Abstract

Diabetes Mellitus is a chronic metabolic disorder characterized by impaired insulin production and/or action, leading to persistent hyperglycemia and insulin resistance. It has been associated with several comorbidities, including cognitive dysfunction, affecting functions such as attention, memory, and processing speed. Mounting evidence indicates a complex relationship between type 2 Diabetes Mellitus (DM2) and neurodegenerative disorders such as mild cognitive impairment and Alzheimer's disease (AD). Beyond the conventional hallmarks of each pathology, patients with DM2 face an increased risk of neuronal degeneration, while AD is characterized by a marked reduction in insulin receptor density. Although aging, neuroinflammation, and vascular dysfunction have been recognized as key risk factors in AD, the precise molecular mechanisms driving AD pathogenesis remain incompletely understood. Various studies have been conducted to identify reliable biomarkers that elucidate the connection between DM2 and AD, including insulin dysregulation, neuroinflammation, amyloid-β aggregation, and tau hyperphosphorylation. Investigation of these biomarkers is still ongoing, and they may serve not only as diagnostic tools but also as therapeutic targets. Here, we review the current evidence supporting a convergent biological framework between DM2 and AD. Clarifying these shared pathways may improve early detection and guide the development of targeted therapeutic strategies aimed at reducing neurodegeneration in metabolically vulnerable populations.

Indexed as

Alzheimer DiseaseDiabetes Mellitus, Type 2Amyloid beta-PeptidesAnimalsBiomarkersCognitive DysfunctionHumansInsulintau ProteinsAmyloid beta-PeptidesBiomarkersInsulintau ProteinsAlzheimer’s diseaseamyloid-βbiomarkerscognitive dysfunctionhyperglycemianeuroinflammationtype 2 diabetes mellitus

Identifiers

PMID41977405
PMCPMC13073904

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.