Evidence map›Paper›PMID 41683694›Full record

ReviewInternational journal of molecular sciences2026

Neurochemical and Energetic Alterations in Depression: A Narrative Review of Potential PET Biomarkers.

Santiago Jose Cornejo Schmiedl, Bryan Astudillo Ortega, Bernardo Sosa-Moscoso, Gabriela González de Armas, Jose Ignacio Montenegro Galarza, Jose A Rodas, Jose E Leon-Rojas

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

7 authors.

Santiago Jose Cornejo SchmiedlNeurALL Research Group, Quito 170157, Ecuador.
Bryan Astudillo OrtegaNeurALL Research Group, Quito 170157, Ecuador.ORCID 0009-0006-2111-8974
Bernardo Sosa-MoscosoNeurALL Research Group, Quito 170157, Ecuador.ORCID 0000-0002-3416-2951
Gabriela González de ArmasEscuela de Medicina, Universidad de Las Américas, Quito 170124, Ecuador.
Jose Ignacio Montenegro GalarzaEscuela de Medicina, Universidad de Las Américas, Quito 170124, Ecuador.
Jose A RodasSchool of Psychology, University College Dublin, D04 V1W8 Dublin, Ireland.ORCID 0000-0001-8217-0238
Jose E Leon-RojasEscuela de Medicina, Universidad de Las Américas, Quito 170124, Ecuador.ORCID 0000-0002-8130-6460

Funding

Universidad de Las Américas 592.A.XVII.25
6 · The paper itself

Abstract

Depression is a heterogeneous neuropsychiatric disorder with variable clinical presentation and response to treatment. This variability has motivated interest in neuroimaging biomarkers capable of disease characterization and therapeutic prediction. Positron emission tomography (PET) enables in vivo assessment of cerebral glucose utilization, neurochemical targets, inflammatory markers, and cerebral blood flow. This narrative review synthesizes PET studies conducted predominantly in adults with major depressive disorder diagnosed using DSM-based criteria, with bipolar disorder included only when imaging was performed during a depressive episode. Studies were identified through a structured, non-systematic literature search of major databases. Depression is consistently associated with regionally specific PET alterations within cortico-limbic and cortico-striatal circuits; studies most frequently report reduced glucose-derived PET measures in prefrontal and anterior cingulate regions at baseline, with treatment responders showing relative increases or redistribution of these measures following interventions. Neurochemical PET studies demonstrate altered receptor, transporter, or enzyme-related binding in serotonergic, dopaminergic, and noradrenergic systems, while neuroinflammatory and perfusion studies reveal regionally increased PET signals in subsets of patients. Overall, PET findings indicate convergent, region-specific and neurochemical alterations associated with depressive episodes and treatment response. Interpretation is constrained by methodological and clinical heterogeneity, underscoring the need for harmonized, longitudinal PET studies.

Indexed as

BiomarkersBrainDepressionMajor Depressive DisorderPositron-Emission TomographyAnimalsGlucoseHumansBiomarkersGlucosebiomarkerbrain metabolismdepressionPETpositron emission tomography

Identifiers

PMID41683694
PMCPMC12898749

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Registered trials

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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 OpenQuestion graph.