Evidence map›Paper›PMID 41041839›Full record

ArticleInternational journal of molecular medicine2025

Changes in the endoplasmic reticulum‑mitochondria communication in dermal fibroblasts from early‑stage bipolar disorder patients: Skin‑brain axis as a new route to understand the pathophysiology of mental illness?

Ana Catarina Pereira, Ana Patrícia Marques, Rosa Resende, Laura Serrano-Cuñarro, Margarida Caldeira, Tânia Fernandes, Mariana Batista, António Macedo, Joana Barbosa De Melo, Nuno Madeira and 3 more

Abstract read
In one paragraph

Article in International journal of molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
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

13 authors.

Ana Catarina PereiraCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Ana Patrícia MarquesCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Rosa ResendeCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Laura Serrano-CuñarroCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Margarida CaldeiraCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Tânia FernandesCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Mariana BatistaClinical and Academic Center of Coimbra (CACC), 3004‑561 Coimbra, Portugal.
António MacedoFaculty of Medicine, University of Coimbra, 3000‑370 Coimbra, Portugal.
Joana Barbosa De MeloFaculty of Medicine, University of Coimbra, 3000‑370 Coimbra, Portugal.
Nuno MadeiraFaculty of Medicine, University of Coimbra, 3000‑370 Coimbra, Portugal.
Cláudia CavadasCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Maria Teresa CruzCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.
Cláudia Fragão PereiraCenter for Neuroscience and Cell Biology (CNC‑UC), Center for Innovative Biomedicine and Biotechnology (CiBB), University of Coimbra, 3004‑504 Coimbra, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compromised cellular resilience in bipolar disorder (BD) has been associated with structural brain changes and cognitive deficits caused by perturbation of redox status, endoplasmic reticulum (ER) stress and innate immunity. These crucial cellular events are regulated by the ER‑mitochondria close contacts at mitochondria‑associated membranes (MAM) through Ca

Indexed as

Bipolar DisorderBrainEndoplasmic ReticulumFibroblastsMitochondriaSkinAdultCalciumEndoplasmic Reticulum StressFemaleHumansInflammasomesMaleMiddle AgedOxidative StressCalciumInflammasomesbipolar disorderendoplasmic reticulummitochondriamitochondria-associated membranesskin fibroblasts

Identifiers

PMID41041839
PMCPMC12513433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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 OpenQuestion graph.